COMPANION-BREED-HEALTH Topics
2006 topics in this category. Every entry is available as a complete static page.
companion_breed_health_abyssinian_late_onset_photoreceptor_degeneration_catAbyssinian — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_abyssinian_omia2795_catAbyssinian — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_abyssinian_omia2929_catAbyssinian — Coat colour, ticked (Abyssinian) (hereditary; OMIA-verified breed predisposition)companion_breed_health_abyssinian_omia3282_catAbyssinian — Nephrotic syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_abyssinian_progressive_retinal_dystrophy_atrophy_cone_rod_dystrophy_dys_catAbyssinian — Progressive retinal dystrophy/atrophy; Cone-rod dystrophy/dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_aegidienberger_germany_horse_neuronal_ceroid_lipofuscinosis_horseAegidienberger, Germany (Horse) — Neuronal ceroid lipofuscinosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_affenpinscher_the_disease_is_also_called_arnold_chiari_malformation_caudal_dogAffenpinscher — Chiari malformation Type I with syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_afghan_hound_omia1311_dogAfghan Hound — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_afghan_hound_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogAfghan Hound — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_airedale_terrier_fatal_neonatal_interstitial_lung_disease_dogAiredale Terrier — Fatal neonatal interstitial lung disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_airedale_terrier_omia1311_dogAiredale Terrier — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_airedale_terrier_omia54_dogAiredale Terrier — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_airedale_terrier_omia647_dogAiredale Terrier — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_akhal_teke_horse_omia4008_horseAkhal-Teke (Horse) — Naked foal syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_akita_omia4093_dogAkita — Macrothrombocytopenia (hereditary; OMIA-verified breed predisposition)companion_breed_health_akita_omia4164_dogAkita — Amelogenesis imperfecta, ACP4-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_alapaha_blue_blood_bulldog_dermatosparaxis_ehlers_danlos_syndrome_deds_adamts2_related__dogAlapaha Blue Blood Bulldog — Dermatosparaxis Ehlers-Danlos syndrome (dEDS), ADAMTS2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaska_rabbit_omia2943_rabbitAlaska (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_husky_alaskan_husky_encephalopathy_ahe_dogAlaskan Husky — Alaskan Husky Encephalopathy (AHE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_husky_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogAlaskan Husky — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_husky_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogAlaskan Husky — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_husky_neuronal_vacuolation_and_spinocerebellar_degeneration_polyne_dogAlaskan Husky — Polyneuropathy, RAB3GAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_husky_omia647_dogAlaskan Husky — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_husky_omia702_dogAlaskan Husky — Gangliosidosis, GM1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_klee_kai_omia647_dogAlaskan Klee Kai — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_malamute_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogAlaskan Malamute — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_malamute_omia1311_dogAlaskan Malamute — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_malamute_omia4052_dogAlaskan Malamute — Polyneuropathy, NDRG1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_malamute_omia4216_dogAlaskan Malamute — Ciliary dyskinesia, primary, NME5-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_malamute_omia54_dogAlaskan Malamute — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_alaskan_malamute_omia647_dogAlaskan Malamute — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_alpine_dachsbracke_omia2977_dogAlpine Dachsbracke — Neuronal ceroid lipofuscinosis, 8 (hereditary; OMIA-verified breed predisposition)companion_breed_health_alpine_dachsbracke_omia4197_dogAlpine Dachsbracke — Ataxia, spinocerebellar, SCN8A-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_altai_dominant_blue_eyes_dbe_catAltai — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_akita_omia4164_dogAmerican Akita — Amelogenesis imperfecta, ACP4-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bobtail_feline_familial_hcm_881_catAmerican Bobtail — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bobtail_feline_familial_hcm_catAmerican Bobtail — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bobtail_manx_tailllessness_catAmerican Bobtail — Manx tailllessness (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bobtail_shorthair_feline_familial_hcm_6367_catAmerican Bobtail Shorthair — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bobtail_shorthair_feline_familial_hcm_catAmerican Bobtail Shorthair — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bulldog_autosomal_recessive_congenital_ichthyosis_dogAmerican Bulldog — autosomal recessive congenital ichthyosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bulldog_canine_multifocal_retinopathy_dogAmerican Bulldog — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bulldog_omia2053_dogAmerican Bulldog — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bulldog_omia2975_dogAmerican Bulldog — Neuronal ceroid lipofuscinosis, 10 (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bulldog_omia4083_dogAmerican Bulldog — Nemaline myopathy, NEB-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bulldog_robinow_like_syndrome_curly_tail_dogAmerican Bulldog — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_bully_autosomal_recessive_congenital_ichthyosis_dogAmerican Bully — autosomal recessive congenital ichthyosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_cocker_spaniel_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogAmerican Cocker Spaniel — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_cocker_spaniel_omia2489_dogAmerican Cocker Spaniel — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_cocker_spaniel_omia3629_dogAmerican Cocker Spaniel — Glaucoma, primary closed-angle (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_cocker_spaniel_omia3925_dogAmerican Cocker Spaniel — Glaucoma, primary open angle (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_cocker_spaniel_omia54_dogAmerican Cocker Spaniel — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_cocker_spaniel_omia729_dogAmerican Cocker Spaniel — Glycogen storage disease VII (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_cocker_spaniel_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogAmerican Cocker Spaniel — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_curl_late_onset_photoreceptor_degeneration_catAmerican Curl — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_curl_scottish_fold_scottish_fold_osteochondrodysplasia_sfocd_oste_catAmerican Curl — Scottish fold, Scottish Fold osteochondrodysplasia (SFOCD), osteodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_eskimo_dog_caldag_gefi_thrombopathia_caldag_gefi_platelet_disorder_dogAmerican Eskimo Dog — CalDAG-GEFI thrombopathia; CalDAG-GEFI platelet disorder (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_eskimo_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogAmerican Eskimo Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_eskimo_dog_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogAmerican Eskimo Dog — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_eskimo_dog_omia2489_dogAmerican Eskimo Dog — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_foxhound_omia2648_dogAmerican Foxhound — Hypocatalasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_foxhound_omia647_dogAmerican Foxhound — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_hairless_terrier_recessive_hairlessness_congenital_alopecia_dogAmerican Hairless Terrier — Recessive hairlessness, congenital alopecia (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_miniature_horse_horse_omia4086_horseAmerican Miniature Horse (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_miniature_horse_horse_silver_dapple_horseAmerican Miniature Horse (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_miniature_horse_horse_splashed_white_macchiato_horseAmerican Miniature Horse (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_equine_rhabdomyolysis_syndrome_polysaccharide_storage_myopat_horseAmerican Paint (Horse) — Equine rhabdomyolysis syndrome; Polysaccharide storage myopathy; Tying-up (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_glycogen_storage_disease_iv_gsd_iv_glycogen_storage_disease__horseAmerican Paint (Horse) — Glycogen storage disease IV (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_omia2113_horseAmerican Paint (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_omia483_horseAmerican Paint (Horse) — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_overo_lethal_white_foal_syndrome_frame_overo_spotting_horseAmerican Paint (Horse) — Overo lethal white foal syndrome; frame overo spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_palomino_horseAmerican Paint (Horse) — Palomino (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_silver_dapple_horseAmerican Paint (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_splashed_white_horseAmerican Paint (Horse) — splashed white (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_splashed_white_macchiato_horseAmerican Paint (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_paint_horse_tobiano_sabino_horseAmerican Paint (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_pit_bull_terrier_dermatosparaxis_ehlers_danlos_syndrome_deds_adamts2_related__dogAmerican Pit Bull Terrier — Dermatosparaxis Ehlers-Danlos syndrome (dEDS), ADAMTS2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_pit_bull_terrier_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogAmerican Pit Bull Terrier — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_pit_bull_terrier_omia3313_dogAmerican Pit Bull Terrier — Retinal atrophy - Cone-rod dystrophy 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_pit_bull_terrier_omia4296_dogAmerican Pit Bull Terrier — Calvarial hyperostotic syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_pit_bull_terrier_omia54_dogAmerican Pit Bull Terrier — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_pit_bull_terrier_robinow_like_syndrome_curly_tail_dogAmerican Pit Bull Terrier — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_pit_bull_terrier_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogAmerican Pit Bull Terrier — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_saddle_horse_horse_also_known_as_epitheliogenesis_imperfecta_horseAmerican Saddle Horse (Horse) — Also known as Epitheliogenesis imperfecta. (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_saddle_horse_horse_omia5331_horseAmerican Saddle Horse (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_saddle_horse_horse_silver_dapple_horseAmerican Saddle Horse (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_shorthair_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catAmerican Shorthair — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_shorthair_feline_familial_hcm_catAmerican Shorthair — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_shorthair_late_onset_photoreceptor_degeneration_catAmerican Shorthair — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_shorthair_omia4466_catAmerican Shorthair — Cardiomyopathy, hypertrophic, ALMS1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_shorthair_omia5690_catAmerican Shorthair — Epidermolysis bullosa, junctionalis, COL17A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_shorthair_omia652_catAmerican Shorthair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_also_called_multiple_osteochondromas_multiple_hereditary_exo_dogAmerican Staffordshire Terrier — Osteochondromatosis, EXT2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_cerebellar_cortical_abiotrophy_cerebellar_cortical_degenerat_dogAmerican Staffordshire Terrier — Lysosomal storage disease, ARSG related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogAmerican Staffordshire Terrier — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_hyperuricosuria_and_hyperuricemia_dogAmerican Staffordshire Terrier — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_omia3312_dogAmerican Staffordshire Terrier — Retinal atrophy - Cone-rod dystrophy 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_omia4296_dogAmerican Staffordshire Terrier — Calvarial hyperostotic syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_procoagulant_expression_canine_platelet_procoagulant_deficie_dogAmerican Staffordshire Terrier — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_robinow_like_syndrome_curly_tail_dogAmerican Staffordshire Terrier — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_ullrich_like_congenital_muscular_dystrophy_sarcolemmal_speci_dogAmerican Staffordshire Terrier — Muscular dystrophy, Ullrich type, COL6A3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_staffordshire_terrier_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogAmerican Staffordshire Terrier — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_toy_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogAmerican Toy Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_trotter_horse_chestnut_horseAmerican Trotter (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_trotter_horse_omia2113_horseAmerican Trotter (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_trotter_horse_omia3380_horseAmerican Trotter (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_trotter_horse_omia3790_horseAmerican Trotter (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_trotter_horse_omia5331_horseAmerican Trotter (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_trotter_horse_splashed_white_macchiato_horseAmerican Trotter (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_trotter_horse_tobiano_sabino_horseAmerican Trotter (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_water_spaniel_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogAmerican Water Spaniel — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_american_wirehair_late_onset_photoreceptor_degeneration_catAmerican Wirehair — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_anatolian_shepherd_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogAnatolian Shepherd Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_anatolian_shepherd_dog_omia1191_dogAnatolian Shepherd Dog — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_anatolian_shepherd_dog_omia604_dogAnatolian Shepherd Dog — Entropion (hereditary; OMIA-verified breed predisposition)companion_breed_health_anglo_arab_horse_tobiano_sabino_horseAnglo-Arab (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_angora_rabbit_omia2902_rabbitAngora (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_angora_rabbit_omia3600_rabbitAngora (Rabbit) — Hair, long (hereditary; OMIA-verified breed predisposition)companion_breed_health_appaloosa_horse_omia2113_horseAppaloosa (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_appaloosa_horse_omia2177_horseAppaloosa (Horse) — Ocular squamous cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_appaloosa_horse_omia4086_horseAppaloosa (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_appaloosa_horse_omia483_horseAppaloosa (Horse) — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_appaloosa_horse_rhabdomyolysis_with_hyperthermia_anesthesia_induced_malignan_horseAppaloosa (Horse) — rhabdomyolysis with hyperthermia; anesthesia-induced malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_appaloosa_horse_splashed_white_horseAppaloosa (Horse) — splashed white (hereditary; OMIA-verified breed predisposition)companion_breed_health_appaloosa_horse_splashed_white_macchiato_horseAppaloosa (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_appaloosa_horse_tobiano_sabino_horseAppaloosa (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_appenzeller_sennenhund_many_alias_names_exist_for_the_phenotype_they_include_congen_dogAppenzeller Sennenhund — Many alias names exist for the phenotype. They include congenital cornification disorder; CHILD nevi; CHILD-like nevi; ILVEN. The human phenotype resulting from NSDHL loss-of-function variants is termed congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD syndrome). CHILD syndrome is characterized by epidermal nevi and striking unilateral limb defects. Animals (dogs, cats, mice) with NSDHL variants have similar epidermal nevi, but so far were never reported to also have the limb defects seen in human CHILD syndrome. (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_chestnut_horseArab (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_omia2113_horseArab (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_omia2313_horseArab (Horse) — Cerebellar abiotrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_omia3790_horseArab (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_omia4491_horseArab (Horse) — Myopathy, myofibrillar (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_omia483_horseArab (Horse) — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_rhabdomyolysis_with_hyperthermia_anesthesia_induced_malignan_horseArab (Horse) — rhabdomyolysis with hyperthermia; anesthesia-induced malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_severe_combined_immunodeficiency_disease_scid_horseArab (Horse) — Severe Combined Immunodeficiency Disease (SCID) (hereditary; OMIA-verified breed predisposition)companion_breed_health_arab_horse_silver_dapple_horseArab (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_ardennes_horse_silver_dapple_horseArdennes (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogAustralian Cattle Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_canine_spongiform_leukoencephalomyelopathy_leucodystrophy_sh_dogAustralian Cattle Dog — Leukodystrophy, CYTB-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_congenital_sensorineural_deafness_dogAustralian Cattle Dog — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_cystine_urolithiasis_dogAustralian Cattle Dog — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_omia1373_dogAustralian Cattle Dog — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_omia2053_dogAustralian Cattle Dog — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_omia2489_dogAustralian Cattle Dog — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_omia2976_dogAustralian Cattle Dog — Neuronal ceroid lipofuscinosis, 5 (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_omia3062_dogAustralian Cattle Dog — Neuronal ceroid lipofuscinosis, 12 (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_omia4461_dogAustralian Cattle Dog — Coat colour, roan (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_omia6303_dogAustralian Cattle Dog — Stomatocytosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogAustralian Cattle Dog — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_procoagulant_expression_canine_platelet_procoagulant_deficie_dogAustralian Cattle Dog — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogAustralian Cattle Dog — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_cattle_dog_x_omia3315_catAustralian Cattle Dog X — Epidermolysis bullosa, junctionalis, LAMA3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_kelpie_cerebellar_ataxia_dogAustralian Kelpie — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_kelpie_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogAustralian Kelpie — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_kelpie_globoid_cell_leukodystrophy_dogAustralian Kelpie — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_kelpie_omia4254_dogAustralian Kelpie — Lipid malabsorption, ACSL5-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_kelpie_omia5594_dogAustralian Kelpie — Lissencephaly, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_koolie_this_is_the_classic_m_merle_locus_little_1957_dogAustralian Koolie — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_labradoodle_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogAustralian Labradoodle — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_bob_tail_bob_tail_dogAustralian Shepherd — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogAustralian Shepherd — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_canine_multifocal_retinopathy_dogAustralian Shepherd — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogAustralian Shepherd — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_hereditary_ataxia_dogAustralian Shepherd — hereditary ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_hyperuricosuria_and_hyperuricemia_dogAustralian Shepherd — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_ivermectin_sensitivity_dogAustralian Shepherd — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_omia1422_dogAustralian Shepherd — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_omia2489_dogAustralian Shepherd — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_omia2977_dogAustralian Shepherd — Neuronal ceroid lipofuscinosis, 8 (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_omia3097_dogAustralian Shepherd — Neuronal ceroid lipofuscinosis, 6 (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_omia4338_dogAustralian Shepherd — Epidermolysis bullosa, junctionalis, LAMB3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_omia5138_dogAustralian Shepherd — Ciliary dyskinesia, primary, STK36-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_omia5345_dogAustralian Shepherd — Hyposegmentation of granulocytes (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_omia957_dogAustralian Shepherd — Intestinal cobalamin malabsorption, AMN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_persistent_hyaloid_artery_pha_dogAustralian Shepherd — Persistent hyaloid artery (PHA) (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_primary_hereditary_cataract_dogAustralian Shepherd — Primary hereditary cataract (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_renal_cancer_syndrome_nodular_dermatofibrosis_and_kidney_dis_dogAustralian Shepherd — Renal cancer syndrome, nodular dermatofibrosis and kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_this_is_the_classic_b_brown_locus_described_by_little_1957_dogAustralian Shepherd — This is the classic B (Brown) locus described by Little (1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_this_is_the_classic_m_merle_locus_little_1957_dogAustralian Shepherd — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_shepherd_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogAustralian Shepherd — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_stumpy_tail_cattle_dog_bob_tail_bob_tail_dogAustralian Stumpy Tail Cattle Dog — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_australian_stumpy_tail_cattle_dog_omia2489_dogAustralian Stumpy Tail Cattle Dog — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_austrian_pinscher_bob_tail_bob_tail_dogAustrian Pinscher — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_balinese_late_onset_photoreceptor_degeneration_catBalinese — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_balinese_omia3786_catBalinese — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_balinese_omia652_catBalinese — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_barbet_omia2489_dogBarbet — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_basenji_omia1422_dogBasenji — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_basenji_omia1515_dogBasenji — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_basenji_omia3638_dogBasenji — Retinal atrophy, progressive, SAG-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_basenji_spontaneous_fanconi_syndrome_idiopathic_fanconi_syndrome_dogBasenji — spontaneous Fanconi syndrome, idiopathic Fanconi syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_bashkir_curly_horse_omia2313_horseBashkir Curly (Horse) — Cerebellar abiotrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_bashkir_curly_horse_omia6786_horseBashkir Curly (Horse) — Curly coat, KRT25-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_bleu_de_gascogne_omia3776_dogBasset Bleu de Gascogne — Neuronal ceroid lipofuscinosis, 7 (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_fauve_de_bretagne_weill_marchesani_like_syndrome_goniodysgenesis_dogBasset Fauve de Bretagne — Weill-Marchesani-like syndrome; goniodysgenesis (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_caldag_gefi_thrombopathia_caldag_gefi_platelet_disorder_dogBasset Hound — CalDAG-GEFI thrombopathia; CalDAG-GEFI platelet disorder (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogBasset Hound — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_globoid_cell_leukodystrophy_dogBasset Hound — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_glycogen_storage_disease_myopathy_dogBasset Hound — glycogen storage disease myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_grey_collie_syndrome_gray_collie_syndrome_dogBasset Hound — Grey Collie Syndrome; Gray Collie Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogBasset Hound — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_omia1293_dogBasset Hound — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_omia1587_dogBasset Hound — Severe combined immunodeficiency disease, X-linked (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_omia3513_dogBasset Hound — Coat colour, saddle tan vs black-and-tan (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_omia3629_dogBasset Hound — Glaucoma, primary closed-angle (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_omia4947_dogBasset Hound — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_omia647_dogBasset Hound — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_persistent_m_llerian_duct_syndrome_dogBasset Hound — Persistent Müllerian Duct Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_weill_marchesani_like_syndrome_goniodysgenesis_dogBasset Hound — Weill-Marchesani-like syndrome; goniodysgenesis (hereditary; OMIA-verified breed predisposition)companion_breed_health_basset_hound_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogBasset Hound — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBeagle — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_cerebellar_ataxia_dogBeagle — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__dogBeagle — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related; Ehlers-Danlos syndrome, classic type, 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogBeagle — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_congenital_stationary_night_blindness_dogBeagle — Congenital stationary night blindness (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_dew_claws_canine_preaxial_polydactyly_dogBeagle — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_fibrinoid_leukodystrophy_fibrinoid_encephalomyelopathy_dogBeagle — Fibrinoid leukodystrophy, fibrinoid encephalomyelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_globoid_cell_leukodystrophy_dogBeagle — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogBeagle — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_invasive_transitional_cell_carcinoma_of_the_bladder_canine_i_dogBeagle — Transitional cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_musladin_lueke_syndrome_chinese_beagle_syndrome_dogBeagle — Musladin-Lueke syndrome, Chinese beagle syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_neonatal_cerebellar_cortical_degeneration_dogBeagle — Neonatal cerebellar cortical degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia1293_dogBeagle — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia1311_dogBeagle — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia1500_dogBeagle — Retinal atrophy, progressive, X-linked, type 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia1515_dogBeagle — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia1851_dogBeagle — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia2648_dogBeagle — Hypocatalasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia3472_dogBeagle — Intestinal cobalamin (vitamin B12) malabsorption, CUBN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia3925_dogBeagle — Glaucoma, primary open angle (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia458_dogBeagle — Corneal dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia54_dogBeagle — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia6303_dogBeagle — Stomatocytosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia647_dogBeagle — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_omia702_dogBeagle — Gangliosidosis, GM1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_procoagulant_expression_canine_platelet_procoagulant_deficie_dogBeagle — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_protein_deletion_dogBeagle — Protein deletion (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_renal_cancer_syndrome_nodular_dermatofibrosis_and_kidney_dis_dogBeagle — Renal cancer syndrome, nodular dermatofibrosis and kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_beagle_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogBeagle — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_beauceron_omia5040_dogBeauceron — Deafness, CDH23-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_bedlington_terrier_copper_toxicosis_atypical_form_of_wilson_disease_dogBedlington Terrier — copper toxicosis, atypical form of Wilson disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_bedlington_terrier_copper_toxicosis_copper_storage_disease_copper_associated_he_dogBedlington Terrier — Wilson disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_bedlington_terrier_hereditary_footpad_hyperkeratosis_dogBedlington Terrier — Hereditary Footpad Hyperkeratosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_draft_horse_chestnut_horseBelgian Draft (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_draft_horse_equine_rhabdomyolysis_syndrome_polysaccharide_storage_myopat_horseBelgian Draft (Horse) — Equine rhabdomyolysis syndrome; Polysaccharide storage myopathy; Tying-up (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_draft_horse_junctional_epidermolysis_bullosa_horseBelgian Draft (Horse) — Junctional epidermolysis bullosa (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_draft_horse_myosin_heavy_chain_myopathy_horseBelgian Draft (Horse) — myosin heavy chain myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_draft_horse_omia2177_horseBelgian Draft (Horse) — Ocular squamous cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_draft_horse_omia838_horseBelgian Draft (Horse) — Hydrocephalus (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_draft_horse_tobiano_sabino_horseBelgian Draft (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBelgian Shepherd Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_cns_atrophy_with_cerebellar_ataxia_dogBelgian Shepherd Dog — CNS atrophy with cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogBelgian Shepherd Dog — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBelgian Shepherd Dog, Malinois — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_classical_haemophilia_hemophilia_dogBelgian Shepherd Dog, Malinois — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogBelgian Shepherd Dog, Malinois — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_dew_claws_canine_preaxial_polydactyly_dogBelgian Shepherd Dog, Malinois — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_leukoencephalomyelopathy_with_oligodendroglial_dysplasia_spi_dogBelgian Shepherd Dog, Malinois — Leukoencephalomyelopathy, NECAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_omia4355_dogBelgian Shepherd Dog, Malinois — Ataxia, spinocerebellar, SLC12A6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_persistent_m_llerian_duct_syndrome_dogBelgian Shepherd Dog, Malinois — Persistent Müllerian Duct Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_procoagulant_expression_canine_platelet_procoagulant_deficie_dogBelgian Shepherd Dog, Malinois — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_malinois_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogBelgian Shepherd Dog, Malinois — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_omia4314_dogBelgian Shepherd Dog — Cardiomyopathy and juvenile mortality (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_omia5551_dogBelgian Shepherd Dog — Ataxia, cerebellar, RALGAPA1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogBelgian Shepherd Dog — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_belgian_shepherd_dog_spongy_degeneration_with_cerebellar_ataxia_2_dogBelgian Shepherd Dog — Spongy degeneration with cerebellar ataxia 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__catBengal — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related; Ehlers-Danlos syndrome, classic type, 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_inherited_retinal_dystrophic_or_degenerative_disorders_early_catBengal — Retinal atrophy, progressive, KIF3B-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_late_onset_photoreceptor_degeneration_catBengal — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_longhair_omia652_catBengal Longhair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_omia2542_catBengal — Hair morphology, glitter (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_omia2795_catBengal — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_omia3732_catBengal — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_omia4955_catBengal — Coat colour and pattern, charcoal, ASIP-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_omia6335_catBengal — Epileptic encephalopathy, CAD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_omia652_catBengal — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_bengal_omia6844_catBengal — Thoracic wall deformity (hereditary; OMIA-verified breed predisposition)companion_breed_health_berber_germany_horse_tobiano_sabino_horseBerber, Germany (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_berger_de_savoie_shepherd_dog_bob_tail_bob_tail_dogBerger de Savoie Shepherd Dog — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_bernese_mountain_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBernese Mountain Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_bernese_mountain_dog_fibrinoid_leukodystrophy_fibrinoid_encephalomyelopathy_dogBernese Mountain Dog — Fibrinoid leukodystrophy, fibrinoid encephalomyelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_bernese_mountain_dog_omia1188_dogBernese Mountain Dog — Histiocytosis, malignant (hereditary; OMIA-verified breed predisposition)companion_breed_health_bernese_mountain_dog_omia1373_dogBernese Mountain Dog — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_bernese_mountain_dog_omia1851_dogBernese Mountain Dog — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_bernese_mountain_dog_references_relating_to_chronic_kidney_disease_are_included_i_dogBernese Mountain Dog — References relating to chronic kidney disease are included in this entry. (hereditary; OMIA-verified breed predisposition)companion_breed_health_bernese_mountain_dog_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogBernese Mountain Dog — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_bhotia_pony_india_horse_omia3380_horseBhotia Pony, India (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_bichon_frise_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogBichon Frise — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_bichon_frise_hyperuricosuria_and_hyperuricemia_dogBichon Frise — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_bichon_frise_omia1191_dogBichon Frise — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_bichon_frise_omia3009_dogBichon Frise — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_bichon_frise_omia54_dogBichon Frise — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_bichon_frise_renal_cancer_syndrome_nodular_dermatofibrosis_and_kidney_dis_dogBichon Frise — Renal cancer syndrome, nodular dermatofibrosis and kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_birman_congenital_hereditary_hypotrichosis_with_short_life_expectan_catBirman — Congenital/hereditary hypotrichosis with short life expectancy (hereditary; OMIA-verified breed predisposition)companion_breed_health_black_and_tan_coonhound_fxiii_dogBlack and Tan Coonhound — FXIII (hereditary; OMIA-verified breed predisposition)companion_breed_health_black_and_tan_coonhound_omia1422_dogBlack and Tan Coonhound — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_black_and_tan_coonhound_omia54_dogBlack and Tan Coonhound — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_black_forest_horse_chestnut_horseBlack Forest (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_black_russian_terrier_hyperuricosuria_and_hyperuricemia_dogBlack Russian Terrier — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_black_russian_terrier_neuronal_vacuolation_and_spinocerebellar_degeneration_polyne_dogBlack Russian Terrier — Polyneuropathy, RAB3GAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_blauer_wiener_rabbit_omia2943_rabbitBlauer Wiener (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_bloodhound_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBloodhound — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_bluetick_coonhound_globoid_cell_leukodystrophy_dogBluetick Coonhound — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_boerboel_canine_multifocal_retinopathy_dogBoerboel — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_boerboel_hyperuricosuria_and_hyperuricemia_dogBoerboel — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_bombay_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__catBombay — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related; Ehlers-Danlos syndrome, classic type, 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_bombay_omia652_catBombay — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_autosomal_dominant_centronuclear_myopathy_dogBorder Collie — Autosomal dominant centronuclear myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBorder Collie — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_cerebellar_ataxia_dogBorder Collie — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_classical_haemophilia_hemophilia_dogBorder Collie — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogBorder Collie — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_congenital_sensorineural_deafness_dogBorder Collie — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_ivermectin_sensitivity_dogBorder Collie — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia1373_dogBorder Collie — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia1422_dogBorder Collie — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia2053_dogBorder Collie — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia2115_dogBorder Collie — Goniodysgenesis (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia2817_dogBorder Collie — Trapped Neutrophil Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia2885_dogBorder Collie — Exercise-induced collapse (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia2976_dogBorder Collie — Neuronal ceroid lipofuscinosis, 5 (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia3393_dogBorder Collie — Deafness, adult-onset (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia3472_dogBorder Collie — Intestinal cobalamin (vitamin B12) malabsorption, CUBN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_omia3872_dogBorder Collie — Dental hypomineralization (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogBorder Collie — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_sensory_neuropathy_hereditary_sensory_and_autonomic_neuropat_dogBorder Collie — Sensory neuropathy; hereditary sensory and autonomic neuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_the_term_inflammatory_bowel_disease_has_been_used_historical_dogBorder Collie — Inflammatory bowel disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_this_is_the_classic_m_merle_locus_little_1957_dogBorder Collie — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogBorder Collie — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_collie_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogBorder Collie — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_terrier_omia655_dogBorder Terrier — Fanconi syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_border_terrier_omia6871_dogBorder Terrier — Phloiokeratosis, SUV39H1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_borzoi_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBorzoi — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_borzoi_dilated_cardiomyopathy_dogBorzoi — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_borzoi_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogBorzoi — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_boston_terrier_mucopolysaccharidosis_i_dogBoston Terrier — Mucopolysaccharidosis I (hereditary; OMIA-verified breed predisposition)companion_breed_health_boston_terrier_omia1422_dogBoston Terrier — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_boston_terrier_omia4053_dogBoston Terrier — Muscular dystrophy, limb-girdle, type R6 (LGMDR6) (hereditary; OMIA-verified breed predisposition)companion_breed_health_boston_terrier_primary_hereditary_cataract_dogBoston Terrier — Primary hereditary cataract (hereditary; OMIA-verified breed predisposition)companion_breed_health_boston_terrier_robinow_like_syndrome_curly_tail_dogBoston Terrier — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_bouvier_des_ardennes_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogBouvier des Ardennes — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_arrhythmogenic_right_ventricular_cardiomyopathy_dogBoxer — Arrhythmogenic right ventricular cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_canine_atopic_dermatitis_cad_dogBoxer — Canine atopic dermatitis (CAD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBoxer — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_cerebellar_ataxia_dogBoxer — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_classical_haemophilia_hemophilia_dogBoxer — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_dilated_cardiomyopathy_dogBoxer — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_omia1785_dogBoxer — Ventricular arrhythmias and sudden death (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_omia1842_dogBoxer — Spondylosis deformans (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_omia1851_dogBoxer — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_omia2053_dogBoxer — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_omia3379_dogBoxer — Cleft lip and palate (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_references_relating_to_chronic_kidney_disease_are_included_i_dogBoxer — References relating to chronic kidney disease are included in this entry. (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_renal_cancer_syndrome_nodular_dermatofibrosis_and_kidney_dis_dogBoxer — Renal cancer syndrome, nodular dermatofibrosis and kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_boxer_the_term_inflammatory_bowel_disease_has_been_used_historical_dogBoxer — Inflammatory bowel disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_boykin_spaniel_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogBoykin Spaniel — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_boykin_spaniel_omia2650_dogBoykin Spaniel — Von Willebrand disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_boykin_spaniel_omia2885_dogBoykin Spaniel — Exercise-induced collapse (hereditary; OMIA-verified breed predisposition)companion_breed_health_braque_du_bourbonnais_bob_tail_bob_tail_dogBraque du Bourbonnais — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_braque_du_bourbonnais_omia3146_dogBraque du Bourbonnais — Exfoliative cutaneous lupus erythematosus (hereditary; OMIA-verified breed predisposition)companion_breed_health_brazilian_terrier_bob_tail_bob_tail_dogBrazilian Terrier — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_brazilian_terrier_omia1258_dogBrazilian Terrier — Mucopolysaccharidosis VII (hereditary; OMIA-verified breed predisposition)companion_breed_health_breton_france_horse_junctional_epidermolysis_bullosa_horseBreton, France (Horse) — Junctional epidermolysis bullosa (hereditary; OMIA-verified breed predisposition)companion_breed_health_briard_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogBriard — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_briard_omia1344_dogBriard — Day blindness (hereditary; OMIA-verified breed predisposition)companion_breed_health_briard_retinal_dystrophy_congenital_stationary_night_blindness_csnb_dogBriard — Retinal dystrophy; congenital stationary night blindness (CSNB) (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_longhair_dominant_blue_eyes_dbe_catBritish Longhair — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_longhair_feline_familial_hcm_catBritish Longhair — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_shorthair_complex_skeletal_dysplasia_catBritish Shorthair — Complex skeletal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_shorthair_dominant_blue_eyes_dbe_catBritish Shorthair — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_shorthair_feline_autoimmune_lymphoproliferative_syndrome_catBritish Shorthair — Feline autoimmune lymphoproliferative syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_shorthair_feline_familial_hcm_catBritish Shorthair — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_shorthair_omia3818_catBritish Shorthair — Brachycephaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_shorthair_omia652_catBritish Shorthair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_shorthair_omia902_catBritish Shorthair — Hypothyroidism, congenital (hereditary; OMIA-verified breed predisposition)companion_breed_health_british_spotted_pony_spotted_pony_united_kingdom_of_great_br_omia4086_horseBritish Spotted Pony, Spotted Pony, United Kingdom of Great Britain and Northern Ireland (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_brittany_spaniel_bob_tail_bob_tail_dogBrittany Spaniel — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_brittany_spaniel_cerebellar_ataxia_dogBrittany Spaniel — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_brittany_spaniel_omia1271_dogBrittany Spaniel — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_brittany_spaniel_omia31_dogBrittany Spaniel — C3 deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_brittany_spaniel_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogBrittany Spaniel — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_brittany_spaniel_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogBrittany Spaniel — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_brussels_griffon_isolated_growth_hormone_deficiency_dogBrussels Griffon — isolated growth hormone deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_brussels_griffon_omia1293_dogBrussels Griffon — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_brussels_griffon_omia2243_dogBrussels Griffon — Syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_brussels_griffon_omia4642_dogBrussels Griffon — Vitreous degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_brussels_griffon_the_disease_is_also_called_arnold_chiari_malformation_caudal_dogBrussels Griffon — Chiari malformation Type I with syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_brussels_griffon_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogBrussels Griffon — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_mastiff_canine_multifocal_retinopathy_dogBull Mastiff — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_mastiff_mitochondrial_fission_encephalopathy_familial_cerebellar_ata_dogBull Mastiff — Mitochondrial fission encephalopathy; familial cerebellar ataxia with hydrocephalus (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_mastiff_omia4296_dogBull Mastiff — Calvarial hyperostotic syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_mastiff_retinitis_pigmentosa_dogBull Mastiff — retinitis pigmentosa (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_mastiff_white_doberman_pinscher_dogBull Mastiff — White Doberman Pinscher (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_terrier_autosomal_dominant_polycystic_kidney_disease_adpkd_bull_terr_dogBull Terrier — Polycystic kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_terrier_congenital_sensorineural_deafness_dogBull Terrier — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_terrier_lethal_acrodermatitis_dogBull Terrier — Lethal acrodermatitis (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_terrier_omia1373_dogBull Terrier — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_terrier_similar_to_alport_syndrome_in_humans_dogBull Terrier — similar to Alport syndrome in humans (hereditary; OMIA-verified breed predisposition)companion_breed_health_bull_terrier_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogBull Terrier — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_bulldog_canine_atopic_dermatitis_cad_dogBulldog — Canine atopic dermatitis (CAD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_bulldog_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogBulldog — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_burmese_burmese_hypokalaemic_periodic_polymyopathy_bhp_catBurmese — Burmese hypokalaemic periodic polymyopathy (BHP) (hereditary; OMIA-verified breed predisposition)companion_breed_health_burmese_omia1487_catBurmese — Hyperoxaluria, primary, type II (Oxalosis II) (hereditary; OMIA-verified breed predisposition)companion_breed_health_burmese_omia2877_catBurmese — Gangliosidosis, GM2, type II (Sandhoff or variant 0) (hereditary; OMIA-verified breed predisposition)companion_breed_health_burmese_omia2929_catBurmese — Coat colour, ticked (Abyssinian) (hereditary; OMIA-verified breed predisposition)companion_breed_health_burmese_omia3818_catBurmese — Brachycephaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_burmese_omia5413_catBurmese — Frontonasal dysplasia, ALX1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_burmese_omia6844_catBurmese — Thoracic wall deformity (hereditary; OMIA-verified breed predisposition)companion_breed_health_burmilla_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catBurmilla — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_cairn_terrier_autosomal_dominant_polycystic_kidney_disease_adpkd_bull_terr_dogCairn Terrier — Polycystic kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_cairn_terrier_globoid_cell_leukodystrophy_dogCairn Terrier — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_cairn_terrier_omia1515_dogCairn Terrier — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_cairn_terrier_omia1851_dogCairn Terrier — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_cairn_terrier_omia2998_dogCairn Terrier — Gallbladder mucoceles (hereditary; OMIA-verified breed predisposition)companion_breed_health_cairn_terrier_omia4947_dogCairn Terrier — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_cairn_terrier_omia54_dogCairn Terrier — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_california_rabbit_omia2902_rabbitCalifornia (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_california_rabbit_omia2943_rabbitCalifornia (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_camarillo_white_horse_united_states_of_america_horse_tobiano_sabino_horseCamarillo White Horse, United States of America (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_canaan_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogCanaan Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_caracal_omia2795_catCaracal — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_cardigan_welsh_corgi_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogCardigan Welsh Corgi — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_cardigan_welsh_corgi_epidermolysis_bullosa_simplex_split_paw_pad_disease_dogCardigan Welsh Corgi — epidermolysis bullosa simplex, split paw pad disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_cardigan_welsh_corgi_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogCardigan Welsh Corgi — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_cardigan_welsh_corgi_omia1587_dogCardigan Welsh Corgi — Severe combined immunodeficiency disease, X-linked (hereditary; OMIA-verified breed predisposition)companion_breed_health_cardigan_welsh_corgi_omia4947_dogCardigan Welsh Corgi — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_cardigan_welsh_corgi_this_is_the_classic_m_merle_locus_little_1957_dogCardigan Welsh Corgi — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_caspian_horse_equine_neuroaxonal_dystrophy_equine_degenerative_myeloenceph_horseCaspian (Horse) — Equine neuroaxonal dystrophy/equine degenerative myeloencephalopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_catahoula_leopard_dog_congenital_sensorineural_deafness_dogCatahoula Leopard Dog — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_catahoula_leopard_dog_dermatosparaxis_ehlers_danlos_syndrome_deds_adamts2_related__dogCatahoula Leopard Dog — Dermatosparaxis Ehlers-Danlos syndrome (dEDS), ADAMTS2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_catahoula_leopard_dog_omia647_dogCatahoula Leopard Dog — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_catahoula_leopard_dog_this_is_the_classic_m_merle_locus_little_1957_dogCatahoula Leopard Dog — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_also_called_episodic_falling_syndrome_episodic_hypertonicity_dogCavalier King Charles Spaniel — Episodic falling, BCAN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_also_known_as_medium_chain_acyl_coa_dehydrogenase_mcad_defic_dogCavalier King Charles Spaniel — Also known as medium-chain acyl-CoA dehydrogenase (MCAD) deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogCavalier King Charles Spaniel — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_copper_toxicosis_copper_storage_disease_copper_associated_he_dogCavalier King Charles Spaniel — Wilson disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_dry_eye_curly_coat_syndrome_dogCavalier King Charles Spaniel — Dry eye curly coat syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogCavalier King Charles Spaniel — Intervertebral disc disease, predisposition to (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_omia1271_dogCavalier King Charles Spaniel — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_omia1851_dogCavalier King Charles Spaniel — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_omia2243_dogCavalier King Charles Spaniel — Syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_omia5896_dogCavalier King Charles Spaniel — Immunodeficiency, CARMIL2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_the_disease_is_also_called_arnold_chiari_malformation_caudal_dogCavalier King Charles Spaniel — Chiari malformation Type I with syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogCavalier King Charles Spaniel — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavalier_king_charles_spaniel_xanthine_urolithiasis_xanthine_nephrolithiasis_dogCavalier King Charles Spaniel — Xanthine urolithiasis; xanthine nephrolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavall_menorqu_spain_horse_splashed_white_macchiato_horseCavall Menorquí, Spain (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_cavallo_agricolo_italiano_da_tiro_pesante_rapido_italy_horse_junctional_epidermolysis_bullosa_horseCavallo Agricolo Italiano da Tiro Pesante Rapido, Italy (Horse) — Junctional epidermolysis bullosa (hereditary; OMIA-verified breed predisposition)companion_breed_health_celestial_dominant_blue_eyes_dbe_catCelestial — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_ch_warmblut_switzerland_horse_tobiano_sabino_horseCH-Warmblut, Switzerland (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_chakouyi_china_horse_omia3380_horseChakouyi, China (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_champagne_silberkaninchen_germany_rabbit_omia2902_rabbitChampagne-Silberkaninchen, Germany (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_champagne_silberkaninchen_germany_rabbit_omia2943_rabbitChampagne-Silberkaninchen, Germany (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_chartreux_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catChartreux — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_checkered_giant_omia2902_rabbitCheckered Giant — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_checkered_giant_omia2943_rabbitCheckered Giant — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_checkered_small_omia2902_rabbitCheckered Small — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_checkered_small_omia2943_rabbitCheckered Small — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_chesapeake_bay_retriever_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogChesapeake Bay Retriever — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_chesapeake_bay_retriever_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogChesapeake Bay Retriever — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_chesapeake_bay_retriever_mps_vi_dogChesapeake Bay Retriever — MPS VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_chesapeake_bay_retriever_omia2489_dogChesapeake Bay Retriever — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chesapeake_bay_retriever_omia2885_dogChesapeake Bay Retriever — Exercise-induced collapse (hereditary; OMIA-verified breed predisposition)companion_breed_health_chesapeake_bay_retriever_omia3009_dogChesapeake Bay Retriever — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_chesapeake_bay_retriever_omia3603_dogChesapeake Bay Retriever — Ectodermal dysplasia/skin fragility syndrome, PKP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_bilateral_anterior_amelia_baa_dogChihuahua — Bilateral anterior amelia (BAA) (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_classical_ehlers_danlos_syndrome_ceds_col5a2_related_ehlers__dogChihuahua — classical Ehlers-Danlos syndrome (cEDS), COL5A2-related; Ehlers-Danlos syndrome, classic type, 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogChihuahua — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_epidermolytic_hyperkeratosis_epidermolytic_ichthyosis_dogChihuahua — Epidermolytic hyperkeratosis; epidermolytic ichthyosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_fibrinoid_leukodystrophy_fibrinoid_encephalomyelopathy_dogChihuahua — Fibrinoid leukodystrophy, fibrinoid encephalomyelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogChihuahua — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_isolated_growth_hormone_deficiency_dogChihuahua — isolated growth hormone deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_many_alias_names_exist_for_the_phenotype_they_include_congen_dogChihuahua — Many alias names exist for the phenotype. They include congenital cornification disorder; CHILD nevi; CHILD-like nevi; ILVEN. The human phenotype resulting from NSDHL loss-of-function variants is termed congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD syndrome). CHILD syndrome is characterized by epidermal nevi and striking unilateral limb defects. Animals (dogs, cats, mice) with NSDHL variants have similar epidermal nevi, but so far were never reported to also have the limb defects seen in human CHILD syndrome. (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogChihuahua — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_omia1293_dogChihuahua — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_omia1515_dogChihuahua — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_omia2489_dogChihuahua — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_omia3776_dogChihuahua — Neuronal ceroid lipofuscinosis, 7 (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_omia5235_dogChihuahua — Ichthyosis, non-epidermolytic, SDR9C7-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_omia5908_dogChihuahua — Leigh syndrome, NDUFS7-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_omia6682_dogChihuahua — Ichthyosis, ALOXE3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_the_disease_is_also_called_arnold_chiari_malformation_caudal_dogChihuahua — Chiari malformation Type I with syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_chihuahua_this_is_the_classic_m_merle_locus_little_1957_dogChihuahua — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinchilla_rabbit_omia12_rabbitChinchilla (Rabbit) — Tremor, X-linked (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_crested_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogChinese Crested — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_crested_canine_ectodermal_dysplasia_dogChinese Crested — Canine ectodermal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_crested_canine_multiple_system_degeneration_striatonigral_and_cerebe_dogChinese Crested — Multiple system degeneration, SERAC1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_crested_omia2489_dogChinese Crested — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_crested_omia2650_dogChinese Crested — Von Willebrand disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_crested_omia3776_dogChinese Crested — Neuronal ceroid lipofuscinosis, 7 (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_crested_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogChinese Crested — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_crested_procoagulant_expression_canine_platelet_procoagulant_deficie_dogChinese Crested — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_shar_pei_congenital_idiopathic_megaesophagus_dogChinese Shar-Pei — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_shar_pei_hyaluronanosis_familial_shar_pei_fever_hereditary_cutaneous__dogChinese Shar-Pei — Periodic Fever Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_shar_pei_non_epidermolytic_ichthyosis_dogChinese Shar-Pei — Non-epidermolytic ichthyosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_shar_pei_omia1484_dogChinese Shar-Pei — Prekallikrein deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_shar_pei_omia604_dogChinese Shar-Pei — Entropion (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_shar_pei_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogChinese Shar-Pei — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_shar_pei_weill_marchesani_like_syndrome_goniodysgenesis_dogChinese Shar-Pei — Weill-Marchesani-like syndrome; goniodysgenesis (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinese_tank_cat_dominant_blue_eyes_dbe_catChinese Tank Cat — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinook_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogChinook — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chinook_omia3653_dogChinook — Chondrodysplasia, disproportionate short-limbed, ITGA10-related' (hereditary; OMIA-verified breed predisposition)companion_breed_health_chow_chow_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogChow Chow — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_chow_chow_omia2053_dogChow Chow — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_chow_chow_omia54_dogChow Chow — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_chow_chow_ridge_hair_ridge_dermoid_cyst_dogChow Chow — ridge; hair ridge; dermoid cyst (hereditary; OMIA-verified breed predisposition)companion_breed_health_cirneco_dell_etna_cirneco_oculo_neurological_syndrome_dogCirneco dell'Etna — Cirneco oculo-neurological syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_clumber_spaniel_omia2765_dogClumber Spaniel — Pyruvate dehydrogenase deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_clydesdale_horse_chestnut_horseClydesdale (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_clydesdale_horse_tobiano_sabino_horseClydesdale (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_cockapoo_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogCockapoo — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_cockapoo_omia1311_dogCockapoo — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_cockapoo_omia2489_dogCockapoo — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_alport_syndrome_x_linked_hereditary_nephropathy_glomerulonep_dogCocker Spaniel — Alport syndrome, X-linked hereditary nephropathy, glomerulonephritis, X- linked nephritis (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_classical_haemophilia_hemophilia_dogCocker Spaniel — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_dew_claws_canine_preaxial_polydactyly_dogCocker Spaniel — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_dilated_cardiomyopathy_dogCocker Spaniel — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogCocker Spaniel — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_omia1191_dogCocker Spaniel — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_omia1311_dogCocker Spaniel — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_omia1373_dogCocker Spaniel — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_omia1422_dogCocker Spaniel — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_omia1851_dogCocker Spaniel — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_omia2053_dogCocker Spaniel — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_omia2998_dogCocker Spaniel — Gallbladder mucoceles (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_omia4217_dogCocker Spaniel — Bernard-Soulier syndrome, type C (hereditary; OMIA-verified breed predisposition)companion_breed_health_cocker_spaniel_persistent_m_llerian_duct_syndrome_dogCocker Spaniel — Persistent Müllerian Duct Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogCollie — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_grey_collie_syndrome_gray_collie_syndrome_dogCollie — Grey Collie Syndrome; Gray Collie Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_ivermectin_sensitivity_dogCollie — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_omia1191_dogCollie — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_omia1366_dogCollie — Optic nerve hypoplasia, bilateral (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_rough_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogCollie Rough — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_rough_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogCollie Rough — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_rough_ivermectin_sensitivity_dogCollie Rough — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_rough_omia4215_dogCollie Rough — Recurrent inflammatory pulmonary disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_rough_this_is_the_classic_m_merle_locus_little_1957_dogCollie Rough — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_collie_smooth_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogCollie Smooth — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_colorpoint_shorthair_late_onset_photoreceptor_degeneration_catColorpoint Shorthair — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_coloured_dwarf_omia2902_rabbitColoured dwarf — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_coloured_dwarf_omia2943_rabbitColoured dwarf — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_comtois_horse_junctional_epidermolysis_bullosa_horseComtois (Horse) — Junctional epidermolysis bullosa (hereditary; OMIA-verified breed predisposition)companion_breed_health_comtois_horse_silver_dapple_horseComtois (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_connemara_pony_horse_also_known_as_hoof_wall_separation_disease_horseConnemara Pony (Horse) — Also known as Hoof Wall Separation Disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_connemara_pony_horse_omia2177_horseConnemara Pony (Horse) — Ocular squamous cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_cornish_rex_late_onset_photoreceptor_degeneration_catCornish Rex — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_cornish_rex_omia3149_catCornish Rex — Vitamin D-deficiency rickets, non-type I, non-type II (hereditary; OMIA-verified breed predisposition)companion_breed_health_coton_de_tulear_bandera_s_neonatal_ataxia_dogCoton de Tulear — Bandera's neonatal ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_coton_de_tulear_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogCoton de Tulear — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_coton_de_tulear_familial_oxalate_nephropathy_dogCoton de Tulear — familial oxalate nephropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_coton_de_tulear_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogCoton de Tulear — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_coton_de_tulear_omia3065_dogCoton de Tulear — Multifocal retinopathy 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_croatian_sheepdog_bob_tail_bob_tail_dogCroatian Sheepdog — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_curly_coated_retriever_omia2885_dogCurly Coated Retriever — Exercise-induced collapse (hereditary; OMIA-verified breed predisposition)companion_breed_health_curly_coated_retriever_omia3009_dogCurly Coated Retriever — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_curly_coated_retriever_omia3100_dogCurly Coated Retriever — Glycogen storage disease IIIa (hereditary; OMIA-verified breed predisposition)companion_breed_health_curly_horse_horse_omia3790_horseCurly Horse (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_curly_horse_horse_omia6786_horseCurly Horse (Horse) — Curly coat, KRT25-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_cymric_omia652_catCymric — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_czechoslovakian_wolfdog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogCzechoslovakian Wolfdog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_czechoslovakian_wolfdog_dwarfism_pituitary_lhx3_related_pituitary_dwarfism_dogCzechoslovakian Wolfdog — Dwarfism, pituitary, LHX3-related; pituitary dwarfism (hereditary; OMIA-verified breed predisposition)companion_breed_health_czechoslovakian_wolfdog_omia569_dogCzechoslovakian Wolfdog — Pituitary hormone deficiency, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_acromelanism_himalayan_coat_color_colour_dogDachshund — Acromelanism; Himalayan coat color/colour (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_brittle_bone_disease_dogDachshund — Brittle bone disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogDachshund — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_congenital_idiopathic_megaesophagus_dogDachshund — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogDachshund — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_miniature_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__dogDachshund, Miniature — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_miniature_dilute_coat_color_with_neurological_defects_dogDachshund, Miniature — Dilute coat color with neurological defects (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_miniature_lgmd2d_alpha_sarcoglycanopathy_dogDachshund, Miniature — LGMD2D; alpha-sarcoglycanopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_miniature_long_haired_early_onset_cone_rod_dystrophy_rpgrip1_crd_dogDachshund, Miniature Long-Haired — Early-onset cone-rod dystrophy, RPGRIP1-CRD (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_miniature_smooth_haired_omia647_dogDachshund, Miniature Smooth-Haired — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_miniature_the_term_inflammatory_bowel_disease_has_been_used_historical_dogDachshund, Miniature — Inflammatory bowel disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_miniature_wire_haired_omia1293_dogDachshund, Miniature Wire-Haired — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_miniature_wire_haired_omia4592_dogDachshund, Miniature Wire-Haired — Afibrinogenaemia, FGA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_omia1311_dogDachshund — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_omia1422_dogDachshund — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_omia1515_dogDachshund — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_omia2901_dogDachshund — Neuronal ceroid lipofuscinosis, 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_omia2974_dogDachshund — Neuronal ceroid lipofuscinosis, 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_omia4947_dogDachshund — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_omia5610_dogDachshund — XY difference of sexual development, HSD17B3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_ridge_hair_ridge_dermoid_cyst_dogDachshund — ridge; hair ridge; dermoid cyst (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogDachshund — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_this_is_the_classic_m_merle_locus_little_1957_dogDachshund — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_dachshund_xanthine_urolithiasis_xanthine_nephrolithiasis_dogDachshund — Xanthine urolithiasis; xanthine nephrolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_dales_horse_foal_immunodeficiency_syndrome_in_fell_and_dales_pony_fell_p_horseDales (Horse) — Foal immunodeficiency syndrome in Fell and Dales Pony; Fell pony syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_also_known_as_acute_respiratory_distress_syndrome_ards_dogDalmatian — Also known as Acute respiratory distress syndrome (ARDS) (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogDalmatian — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_congenital_sensorineural_deafness_dogDalmatian — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_copper_toxicosis_copper_storage_disease_copper_associated_he_dogDalmatian — Wilson disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_dalmatian_leukodystrophy_miniature_poodle_demyelination_dogDalmatian — Dalmatian leukodystrophy; miniature poodle demyelination (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_globoid_cell_leukodystrophy_dogDalmatian — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_hyperuricosuria_and_hyperuricemia_dogDalmatian — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_omia4239_dogDalmatian — Leukodystrophy, cavitating (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_omia4767_dogDalmatian — Dwarfism, PRKG2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_omia5063_dogDalmatian — Lysosomal storage disease, CNP-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_omia5072_dogDalmatian — Iris sphincter dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_references_relating_to_chronic_kidney_disease_are_included_i_dogDalmatian — References relating to chronic kidney disease are included in this entry. (hereditary; OMIA-verified breed predisposition)companion_breed_health_dalmatian_similar_to_alport_syndrome_in_humans_dogDalmatian — similar to Alport syndrome in humans (hereditary; OMIA-verified breed predisposition)companion_breed_health_dandie_dinmont_terrier_omia3629_dogDandie Dinmont Terrier — Glaucoma, primary closed-angle (hereditary; OMIA-verified breed predisposition)companion_breed_health_dandie_dinmont_terrier_omia4947_dogDandie Dinmont Terrier — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_danish_swedish_farm_dog_bob_tail_bob_tail_dogDanish/swedish Farm Dog — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_danish_swedish_farm_dog_omia1422_dogDanish/swedish Farm Dog — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_deutscher_wachtelhund_omia729_dogDeutscher Wachtelhund — Glycogen storage disease VII (hereditary; OMIA-verified breed predisposition)companion_breed_health_devon_rex_devon_rex_catDevon Rex — Devon rex (hereditary; OMIA-verified breed predisposition)companion_breed_health_devon_rex_feline_familial_hcm_catDevon Rex — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_devon_rex_late_onset_photoreceptor_degeneration_catDevon Rex — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_devon_rex_omia652_catDevon Rex — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_bob_tail_bob_tail_dogDoberman Pinscher — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogDoberman Pinscher — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogDoberman Pinscher — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_copper_toxicosis_copper_storage_disease_copper_associated_he_dogDoberman Pinscher — Wilson disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_dermatosparaxis_ehlers_danlos_syndrome_deds_adamts2_related__dogDoberman Pinscher — Dermatosparaxis Ehlers-Danlos syndrome (dEDS), ADAMTS2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_dilated_cardiomyopathy_dogDoberman Pinscher — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_dings_dogDoberman Pinscher — DINGS (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogDoberman Pinscher — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_mucopolysaccharidosis_i_dogDoberman Pinscher — Mucopolysaccharidosis I (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_omia1191_dogDoberman Pinscher — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_omia1311_dogDoberman Pinscher — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_omia1978_dogDoberman Pinscher — Polyglandular autoimmune syndrome, type II (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_omia3879_dogDoberman Pinscher — Ligneous membranitis (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_omia4199_dogDoberman Pinscher — Deafness, unilateral and vestibular dysfunction, PTPRQ-related' (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_omia54_dogDoberman Pinscher — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_omia5641_dogDoberman Pinscher — Mannosidosis, alpha (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_white_doberman_pinscher_dogDoberman Pinscher — White Doberman Pinscher (hereditary; OMIA-verified breed predisposition)companion_breed_health_doberman_pinscher_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogDoberman Pinscher — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_dogo_argentino_congenital_sensorineural_deafness_dogDogo Argentino — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_dogo_argentino_omia1311_dogDogo Argentino — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_dogo_argentino_omia4767_dogDogo Argentino — Dwarfism, PRKG2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dogue_de_bordeaux_canine_multifocal_retinopathy_dogDogue de Bordeaux — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_dogue_de_bordeaux_omia1373_dogDogue de Bordeaux — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_dogue_de_bordeaux_omia3993_dogDogue de Bordeaux — Palmoplantar keratoderma, nonepidermolytic, focal 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_dogue_de_bordeaux_robinow_like_syndrome_curly_tail_dogDogue de Bordeaux — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_longhair_l_2_hydroxyglutaric_aciduria_l_2_hga_catDomestic Longhair — L-2-hydroxyglutaric aciduria (L-2-HGA) (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_longhair_omia1199_catDomestic Longhair — Mannosidosis, alpha (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_longhair_omia2514_catDomestic Longhair — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_longhair_omia2820_catDomestic Longhair — Vitamin D-deficiency rickets, type II (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_longhair_omia3786_catDomestic Longhair — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_longhair_omia4040_catDomestic Longhair — Leukocyte adhesion deficiency, type I (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_longhair_omia5085_catDomestic Longhair — Pyknodysostosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_longhair_omia902_catDomestic Longhair — Hypothyroidism, congenital (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_medium_hair_congenital_adrenal_hypoplasia_cah_catDomestic Medium Hair — Congenital adrenal hypoplasia (CAH) (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_medium_hair_omia3786_catDomestic Medium Hair — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_medium_hair_omia902_catDomestic Medium Hair — Hypothyroidism, congenital (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__catDomestic Shorthair — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_congenital_adrenal_hypoplasia_cah_catDomestic Shorthair — Congenital adrenal hypoplasia (CAH) (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_hereditary_factor_xi_deficiency_congenital_factor_xi_deficie_catDomestic Shorthair — Hereditary factor XI deficiency; congenital factor XI deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_l_2_hydroxyglutaric_aciduria_l_2_hga_catDomestic Shorthair — L-2-hydroxyglutaric aciduria (L-2-HGA) (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_many_alias_names_exist_for_the_phenotype_they_include_congen_catDomestic Shorthair — Many alias names exist for the phenotype. They include congenital cornification disorder; CHILD nevi; CHILD-like nevi; ILVEN. The human phenotype resulting from NSDHL loss-of-function variants is termed congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD syndrome). CHILD syndrome is characterized by epidermal nevi and striking unilateral limb defects. Animals (cats, dogs, mice) with NSDHL variants have similar epidermal nevi, but so far were never reported to also have the limb defects seen in human CHILD syndrome. (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia1199_catDomestic Shorthair — Mannosidosis, alpha (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia1252_catDomestic Shorthair — Mucopolysaccharidosis I (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia1255_catDomestic Shorthair — Mucopolysaccharidosis VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia1459_catDomestic Shorthair — Polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia1713_catDomestic Shorthair — Androgen insensitivity syndrome (AIS) (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia2228_catDomestic Shorthair — Mucolipidosis II (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia2514_catDomestic Shorthair — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia2820_catDomestic Shorthair — Vitamin D-deficiency rickets, type II (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia2877_catDomestic Shorthair — Gangliosidosis, GM2, type II (Sandhoff or variant 0) (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia2941_catDomestic Shorthair — Porphyria, congenital erythropoietic (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia2942_catDomestic Shorthair — Porphyria, acute intermittent (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia3164_catDomestic Shorthair — Muscular dystrophy, limb-girdle, type R4 (LGMDR4) (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia3459_catDomestic Shorthair — Gyrate atrophy of choroid and retina (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia3786_catDomestic Shorthair — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia37_catDomestic Shorthair — Dermatosparaxis Ehlers-Danlos syndrome (dEDS), ADAMTS2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia3881_catDomestic Shorthair — Cystinuria, type I - A (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4082_catDomestic Shorthair — Goldenhar syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4233_catDomestic Shorthair — Cardiomyopathy, hypertrophic, MYH7-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4250_catDomestic Shorthair — Vitamin D-deficiency rickets, type IB (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4273_catDomestic Shorthair — Neuronal ceroid lipofuscinosis, 7 (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4293_catDomestic Shorthair — Methaemoglobinaemia, CYB5R3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4389_catDomestic Shorthair — Epidermolysis bullosa, simplex, KRT14-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4405_catDomestic Shorthair — Thrombasthenia (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4746_catDomestic Shorthair — Hair shaft dysplasia, DSG4-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia4934_catDomestic Shorthair — Osteogenesis imperfecta, CREB3L1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia5280_catDomestic Shorthair — Sebaceous gland dysplasia, SOAT1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia5648_catDomestic Shorthair — Mannosidosis, beta (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia6028_catDomestic Shorthair — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia652_catDomestic Shorthair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia6805_catDomestic Shorthair — Osteogenesis imperfecta, BMP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia681_catDomestic Shorthair — Fibrodysplasia ossificans (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia724_catDomestic Shorthair — Glycogen storage disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_omia902_catDomestic Shorthair — Hypothyroidism, congenital (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_osteomalacia_catDomestic Shorthair — Osteomalacia (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_testicular_hypoplasia_and_persistent_primary_dentition_catDomestic Shorthair — Testicular Hypoplasia and Persistent Primary Dentition (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_x_linked_muscular_dystrophy_catDomestic Shorthair — X-linked muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_domestic_shorthair_xdh_deficiency_xanthine_uroliths_urolithiasis_catDomestic Shorthair — XDH deficiency; xanthine uroliths; urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_donggyeongi_republic_of_korea_bob_tail_bob_tail_dogDonggyeongi, Republic of Korea — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_donskoy_late_onset_photoreceptor_degeneration_catDonskoy — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_donskoy_omia652_catDonskoy — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_donskoy_pink_eye_catDonskoy — Pink-eye (hereditary; OMIA-verified breed predisposition)companion_breed_health_dutch_rabbit_omia2902_rabbitDutch (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_dutch_rabbit_omia2943_rabbitDutch (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_dutch_shepherd_cerebellar_degeneration_myositis_complex_inflammatory_myopat_dogDutch Shepherd — Cerebellar degeneration-myositis complex, inflammatory myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_dutch_tulip_hound_omia4475_dogDutch Tulip Hound — Dyskinesia, paroxysmal, SOD1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_dwarf_long_haired_omia554_rabbitDwarf, long-haired — Dwarfism, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_egyptian_mau_omia2542_catEgyptian Mau — Hair morphology, glitter (hereditary; OMIA-verified breed predisposition)companion_breed_health_egyptian_mau_omia2795_catEgyptian Mau — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_elf_omia652_catElf — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_bulldog_canine_multifocal_retinopathy_dogEnglish Bulldog — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_bulldog_cerebellar_ataxia_dogEnglish Bulldog — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_bulldog_cystine_urolithiasis_dogEnglish Bulldog — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_bulldog_hyperuricosuria_and_hyperuricemia_dogEnglish Bulldog — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_bulldog_robinow_like_syndrome_curly_tail_dogEnglish Bulldog — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_autosomal_recessive_hereditary_nephropathy_alport_syndrome_a_dogEnglish Cocker Spaniel — Nephropathy, COL4A4 related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_congenital_sensorineural_deafness_dogEnglish Cocker Spaniel — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_dilated_cardiomyopathy_dogEnglish Cocker Spaniel — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_omia2489_dogEnglish Cocker Spaniel — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_omia4333_dogEnglish Cocker Spaniel — Coat colour, ticked (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_omia4461_dogEnglish Cocker Spaniel — Coat colour, roan (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_omia4520_dogEnglish Cocker Spaniel — Retinal dysplasia, NDP-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_omia5195_dogEnglish Cocker Spaniel — Pseudomyotonia, paradoxical, SLC7A10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_omia729_dogEnglish Cocker Spaniel — Glycogen storage disease VII (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_retinopathy_with_vitamin_e_deficiency_central_progressive_re_dogEnglish Cocker Spaniel — Ataxia with isolated vitamin E deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_shaking_pup_dogEnglish Cocker Spaniel — Shaking pup (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_x_linked_progressive_retinal_atrophy_dogEnglish Cocker Spaniel — X-linked progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_xanthine_urolithiasis_xanthine_nephrolithiasis_dogEnglish Cocker Spaniel — Xanthine urolithiasis; xanthine nephrolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_cocker_spaniel_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogEnglish Cocker Spaniel — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_foxhound_omia2648_dogEnglish Foxhound — Hypocatalasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_foxhound_omia647_dogEnglish Foxhound — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_lop_omia2902_rabbitEnglish Lop — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_mastiff_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogEnglish Mastiff — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_mastiff_canine_multifocal_retinopathy_dogEnglish Mastiff — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_mastiff_omia1384_dogEnglish Mastiff — Osteogenesis imperfecta, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_mastiff_retinitis_pigmentosa_dogEnglish Mastiff — retinitis pigmentosa (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_pointer_hereditary_sensory_neuropathy_dogEnglish Pointer — hereditary sensory neuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_setter_also_described_as_epidermal_acantholysis_dogEnglish Setter — Also described as epidermal acantholysis (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_setter_congenital_sensorineural_deafness_dogEnglish Setter — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_setter_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogEnglish Setter — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_setter_omia2977_dogEnglish Setter — Neuronal ceroid lipofuscinosis, 8 (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_shepherd_progressive_retinal_atrophy_3_pra3_tibetan_terrier_progressi_dogEnglish Shepherd — Retinal atrophy, progressive, FAM161A-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_spot_rabbit_omia2902_rabbitEnglish Spot (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_spot_rabbit_omia2943_rabbitEnglish Spot (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_spotted_pony_australia_horse_omia4086_horseEnglish Spotted Pony, Australia (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_autosomal_recessive_hereditary_nephropathy_alport_syndrome_a_dogEnglish Springer Spaniel — Nephropathy, COL4A4 related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogEnglish Springer Spaniel — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_early_onset_cone_rod_dystrophy_rpgrip1_crd_dogEnglish Springer Spaniel — Early-onset cone-rod dystrophy, RPGRIP1-CRD (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_hereditary_sensory_neuropathy_dogEnglish Springer Spaniel — hereditary sensory neuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_hyperfibrinolysis_dogEnglish Springer Spaniel — Hyperfibrinolysis (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogEnglish Springer Spaniel — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_jack_russel_terrier_type_congenital_myasthenic_syndrome_post_dogEnglish Springer Spaniel — Myasthenic syndrome, congenital, CHRNE-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia1191_dogEnglish Springer Spaniel — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia4296_dogEnglish Springer Spaniel — Calvarial hyperostotic syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia4333_dogEnglish Springer Spaniel — Coat colour, ticked (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia4980_dogEnglish Springer Spaniel — Dyserythropoietic anemia and myopathy syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia5195_dogEnglish Springer Spaniel — Pseudomyotonia, paradoxical, SLC7A10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia5516_dogEnglish Springer Spaniel — Long QT syndrome, KCNQ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia650_dogEnglish Springer Spaniel — Factor XI deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia693_dogEnglish Springer Spaniel — Fucosidosis, alpha (hereditary; OMIA-verified breed predisposition)companion_breed_health_english_springer_spaniel_omia702_dogEnglish Springer Spaniel — Gangliosidosis, GM1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_entlebucher_mountain_dog_omia2489_dogEntlebucher Mountain Dog — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_entlebucher_mountain_dog_omia3660_dogEntlebucher Mountain Dog — Ectopic ureter (hereditary; OMIA-verified breed predisposition)companion_breed_health_entlebucher_mountain_dog_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogEntlebucher Mountain Dog — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_eurasier_dandy_walker_like_malformation_inferior_cerebellar_hypoplasi_dogEurasier — Dandy-Walker-like malformation; inferior cerebellar hypoplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_eurasier_omia5797_dogEurasier — Polioencephalopathy, MECR-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_european_shorthair_late_onset_photoreceptor_degeneration_catEuropean Shorthair — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_european_shorthair_omia2795_catEuropean Shorthair — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_european_shorthair_omia55_catEuropean Shorthair — Haemophilia A (hereditary; OMIA-verified breed predisposition)companion_breed_health_european_shorthair_omia5690_catEuropean Shorthair — Epidermolysis bullosa, junctionalis, COL17A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_exotic_shorthair_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catExotic Shorthair — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_exotic_shorthair_omia3818_catExotic Shorthair — Brachycephaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_exotic_shorthair_omia4466_catExotic Shorthair — Cardiomyopathy, hypertrophic, ALMS1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_exotic_shorthair_omia652_catExotic Shorthair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_faeroes_pony_horse_omia3790_horseFaeroes Pony (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_fairly_pearly_omia2943_rabbitFairly Pearly — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_fauve_de_borgogne_rabbit_omia2902_rabbitFauve de Borgogne (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_fell_pony_horse_foal_immunodeficiency_syndrome_in_fell_and_dales_pony_fell_p_horseFell Pony (Horse) — Foal immunodeficiency syndrome in Fell and Dales Pony; Fell pony syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_finnish_hound_omia1851_dogFinnish Hound — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_finnish_hound_omia3348_dogFinnish Hound — Ataxia, cerebellar, progressive early-onset, SEL1L-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_finnish_hound_omia647_dogFinnish Hound — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_finnish_lapphund_omia1384_dogFinnish Lapphund — Osteogenesis imperfecta, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_finnish_lapphund_omia2489_dogFinnish Lapphund — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_finnish_lapphund_omia3066_dogFinnish Lapphund — Multifocal retinopathy 3 (hereditary; OMIA-verified breed predisposition)companion_breed_health_finnish_lapphund_omia4473_dogFinnish Lapphund — Retinal atrophy, progressive, IFT122-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_finnish_lapphund_omia726_dogFinnish Lapphund — Glycogen storage disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_fjord_horse_omia3790_horseFjord (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_flat_coated_retriever_omia1188_dogFlat-Coated Retriever — Histiocytosis, malignant (hereditary; OMIA-verified breed predisposition)companion_breed_health_flat_coated_retriever_omia3869_dogFlat-Coated Retriever — Obesity (hereditary; OMIA-verified breed predisposition)companion_breed_health_flemish_giant_rabbit_omia2841_rabbitFlemish Giant (Rabbit) — Yellow fat (hereditary; OMIA-verified breed predisposition)companion_breed_health_foldex_scottish_fold_scottish_fold_osteochondrodysplasia_sfocd_oste_catFoldex — Scottish fold, Scottish Fold osteochondrodysplasia (SFOCD), osteodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_fox_terrier_congenital_idiopathic_megaesophagus_dogFox Terrier — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_foxhound_omia1422_dogFoxhound — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_freiberger_horse_chestnut_horseFreiberger (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_freiberger_horse_congenital_liver_fibrosis_horseFreiberger (Horse) — Congenital liver fibrosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_freiberger_horse_hypertriglyceridemia_induced_pancreatitis_horseFreiberger (Horse) — Hypertriglyceridemia-induced pancreatitis (hereditary; OMIA-verified breed predisposition)companion_breed_health_freiberger_horse_splashed_white_macchiato_horseFreiberger (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_freiberger_horse_tobiano_sabino_horseFreiberger (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogFrench Bulldog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_congenital_hypothyroidism_with_goiter_dogFrench Bulldog — Congenital hypothyroidism with goiter (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_cystine_urolithiasis_dogFrench Bulldog — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_fibrinoid_leukodystrophy_fibrinoid_encephalomyelopathy_dogFrench Bulldog — Fibrinoid leukodystrophy, fibrinoid encephalomyelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogFrench Bulldog — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_omia1293_dogFrench Bulldog — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_omia2053_dogFrench Bulldog — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_omia2243_dogFrench Bulldog — Syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_omia4351_dogFrench Bulldog — Coat colour, HPS3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_omia54_dogFrench Bulldog — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_omia5907_dogFrench Bulldog — Muscle hypertrophy, dysphagia, and gait abnormalities (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_primary_hereditary_cataract_dogFrench Bulldog — Primary hereditary cataract (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_ridge_hair_ridge_dermoid_cyst_dogFrench Bulldog — ridge; hair ridge; dermoid cyst (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_robinow_like_syndrome_curly_tail_dogFrench Bulldog — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_the_term_inflammatory_bowel_disease_has_been_used_historical_dogFrench Bulldog — Inflammatory bowel disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_this_is_the_classic_m_merle_locus_little_1957_dogFrench Bulldog — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_bulldog_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogFrench Bulldog — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_spaniel_hereditary_sensory_neuropathy_dogFrench Spaniel — hereditary sensory neuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_french_trotter_horse_omia3380_horseFrench Trotter (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_friesian_horse_omia3960_horseFriesian (Horse) — Dwarfism, B4GALT7-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_friesian_horse_omia4842_horseFriesian (Horse) — Azoospermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_friesian_horse_omia838_horseFriesian (Horse) — Hydrocephalus (hereditary; OMIA-verified breed predisposition)companion_breed_health_frisian_water_dog_omia3096_dogFrisian Water Dog — Severe combined immunodeficiency disease, autosomal, T cell-negative, B cell-negative, NK cell-positive (hereditary; OMIA-verified breed predisposition)companion_breed_health_galgo_espa_ol_omia4152_dogGalgo Español — Bald thigh syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_hunting_terrier_hyperuricosuria_and_hyperuricemia_dogGerman Hunting Terrier — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_hunting_terrier_omia4089_dogGerman Hunting Terrier — Exercise induced metabolic myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_hunting_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogGerman Hunting Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_longhaired_pointer_omia4590_dogGerman Longhaired Pointer — Thyroid follicular cell carcinoma, predisposition to (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_pinscher_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogGerman Pinscher — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_pinscher_omia723_dogGerman Pinscher — Glycogen storage disease Ia (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_pinscher_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogGerman Pinscher — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_pinscher_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogGerman Pinscher — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_pointer_omia3315_dogGerman Pointer — Epidermolysis bullosa, junctionalis, LAMA3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_riding_pony_horse_tobiano_sabino_horseGerman Riding Pony (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_canine_atopic_dermatitis_cad_dogGerman Shepherd Dog — Canine atopic dermatitis (CAD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogGerman Shepherd Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__dogGerman Shepherd Dog — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_classical_haemophilia_hemophilia_dogGerman Shepherd Dog — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogGerman Shepherd Dog — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_congenital_idiopathic_megaesophagus_cim_dogGerman Shepherd Dog — congenital idiopathic megaesophagus, CIM (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogGerman Shepherd Dog — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_dwarfism_pituitary_lhx3_related_pituitary_dwarfism_dogGerman Shepherd Dog — Dwarfism, pituitary, LHX3-related; pituitary dwarfism (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogGerman Shepherd Dog — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_epidermolysis_bullosa_simplex_split_paw_pad_disease_dogGerman Shepherd Dog — epidermolysis bullosa simplex, split paw pad disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_german_shepherd_dog_pyoderma_dogGerman Shepherd Dog — German Shepherd dog pyoderma (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_hyperuricosuria_and_hyperuricemia_dogGerman Shepherd Dog — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_ivermectin_sensitivity_dogGerman Shepherd Dog — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia1191_dogGerman Shepherd Dog — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia1258_dogGerman Shepherd Dog — Mucopolysaccharidosis VII (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia1384_dogGerman Shepherd Dog — Osteogenesis imperfecta, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia1422_dogGerman Shepherd Dog — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia1785_dogGerman Shepherd Dog — Ventricular arrhythmias and sudden death (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia2999_dogGerman Shepherd Dog — Leukocyte adhesion deficiency, type III (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia3116_dogGerman Shepherd Dog — Anal furunculosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia4011_dogGerman Shepherd Dog — Ichthyosis, ASPRV1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia4184_dogGerman Shepherd Dog — Mannosidosis, beta (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia54_dogGerman Shepherd Dog — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_omia569_dogGerman Shepherd Dog — Pituitary hormone deficiency, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_persistent_m_llerian_duct_syndrome_dogGerman Shepherd Dog — Persistent Müllerian Duct Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_procoagulant_expression_canine_platelet_procoagulant_deficie_dogGerman Shepherd Dog — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_renal_cancer_syndrome_nodular_dermatofibrosis_and_kidney_dis_dogGerman Shepherd Dog — Renal cancer syndrome, nodular dermatofibrosis and kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_shaking_puppy_syndrome_dogGerman Shepherd Dog — Shaking puppy syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_the_term_inflammatory_bowel_disease_has_been_used_historical_dogGerman Shepherd Dog — Inflammatory bowel disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_this_entry_includes_information_about_primary_hyperparathyro_dogGerman Shepherd Dog — This entry includes information about primary hyperparathyroidism (PHPT) (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_this_is_the_classic_b_brown_locus_described_by_little_1957_dogGerman Shepherd Dog — This is the classic B (Brown) locus described by Little (1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_dog_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogGerman Shepherd Dog — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shepherd_hip_dysplasia_dogGerman Shepherd Dog — Hip Dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_classical_haemophilia_hemophilia_dogGerman Shorthaired Pointer — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_hereditary_sensory_neuropathy_dogGerman Shorthaired Pointer — hereditary sensory neuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia1271_dogGerman Shorthaired Pointer — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia1373_dogGerman Shorthaired Pointer — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia2650_dogGerman Shorthaired Pointer — Von Willebrand disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia2977_dogGerman Shorthaired Pointer — Neuronal ceroid lipofuscinosis, 8 (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia3146_dogGerman Shorthaired Pointer — Exfoliative cutaneous lupus erythematosus (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia4075_dogGerman Shorthaired Pointer — Lethality, BTBD17-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia4461_dogGerman Shorthaired Pointer — Coat colour, roan (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia458_dogGerman Shorthaired Pointer — Corneal dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia4758_dogGerman Shorthaired Pointer — Epidermolysis bullosa, junctionalis (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_omia647_dogGerman Shorthaired Pointer — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogGerman Shorthaired Pointer — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_shorthaired_pointer_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogGerman Shorthaired Pointer — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_spitz_omia2650_dogGerman Spitz — Von Willebrand disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_spitz_omia4067_dogGerman Spitz — Oculocutaneous albinism, OCA2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_spitz_omia5196_dogGerman Spitz — Retinal atrophy, progressive, GUCY2D-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_spitz_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogGerman Spitz — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_spitz_sensory_neuropathy_hereditary_sensory_and_autonomic_neuropat_dogGerman Spitz — Sensory neuropathy; hereditary sensory and autonomic neuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_wirehaired_pointer_omia2650_dogGerman Wirehaired Pointer — Von Willebrand disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_wirehaired_pointer_omia458_dogGerman Wirehaired Pointer — Corneal dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_wirehaired_pointer_omia54_dogGerman Wirehaired Pointer — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_german_wirehaired_pointer_omia647_dogGerman Wirehaired Pointer — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_grey_omia2902_rabbitGiant Grey — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_grey_omia2943_rabbitGiant Grey — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_schnauzer_congenital_hypothyroidism_with_goiter_dogGiant Schnauzer — Congenital hypothyroidism with goiter (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_schnauzer_hyperuricosuria_and_hyperuricemia_dogGiant Schnauzer — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_schnauzer_omia1311_dogGiant Schnauzer — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_schnauzer_omia3473_dogGiant Schnauzer — Squamous cell carcinoma of the digit (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_schnauzer_omia4202_dogGiant Schnauzer — Retinal atrophy, progressive, NECAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_schnauzer_omia4561_dogGiant Schnauzer — Cardiomyopathy, dilated, RBM20-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_schnauzer_omia647_dogGiant Schnauzer — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_giant_schnauzer_omia957_dogGiant Schnauzer — Intestinal cobalamin malabsorption, AMN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_glen_of_imaal_terrier_progressive_retinal_atrophy_pra_crd3_dogGlen of Imaal Terrier — Progressive retinal atrophy; PRA-crd3 (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogGolden Retriever — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_cd_dogGolden Retriever — CD (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__dogGolden Retriever — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_classical_haemophilia_hemophilia_dogGolden Retriever — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_congenital_eye_malformation_microphthalmos_dogGolden Retriever — Congenital eye malformation; microphthalmos (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_congenital_hypomyelinating_polyneuropathy_hpn_5455_dogGolden Retriever — congenital hypomyelinating polyneuropathy; HPN (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_congenital_hypomyelinating_polyneuropathy_hpn_5485_dogGolden Retriever — congenital hypomyelinating polyneuropathy; HPN (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_congenital_hypomyelinating_polyneuropathy_hpn_dogGolden Retriever — congenital hypomyelinating polyneuropathy; HPN (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_congenital_myasthenic_syndromes_dogGolden Retriever — Congenital myasthenic syndromes (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogGolden Retriever — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_golden_retriever_ichthyosis_type_2_dogGolden Retriever — Golden Retriever ichthyosis type 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_golden_retriever_pra_2_golden_retriever_progressive_retinal__dogGolden Retriever — Golden Retriever PRA 2, Golden Retriever progressive retinal atrophy 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_hereditary_spectrin_deficiency_dogGolden Retriever — Hereditary spectrin deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_hip_dysplasia_dogGolden Retriever — Hip Dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_mucopolysaccharidosis_i_dogGolden Retriever — Mucopolysaccharidosis I (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia1188_dogGolden Retriever — Histiocytosis, malignant (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia1191_dogGolden Retriever — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia1271_dogGolden Retriever — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia1373_dogGolden Retriever — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia1851_dogGolden Retriever — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia2489_dogGolden Retriever — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia2976_dogGolden Retriever — Neuronal ceroid lipofuscinosis, 5 (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia3364_dogGolden Retriever — Gangliosidosis, GM2, type II (Sandhoff or variant 0) (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia3603_dogGolden Retriever — Ectodermal dysplasia/skin fragility syndrome, PKP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia3879_dogGolden Retriever — Ligneous membranitis (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia4063_dogGolden Retriever — Osteogenesis imperfecta, type III, COL1A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_omia54_dogGolden Retriever — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_renal_cancer_syndrome_nodular_dermatofibrosis_and_kidney_dis_dogGolden Retriever — Renal cancer syndrome, nodular dermatofibrosis and kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_this_entry_was_previously_called_ichthyosis_golden_retriever_dogGolden Retriever — This entry was previously called Ichthyosis, Golden Retriever (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogGolden Retriever — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_golden_retriever_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogGolden Retriever — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_goldendoodle_congenital_idiopathic_megaesophagus_dogGoldendoodle — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_goldendoodle_omia2489_dogGoldendoodle — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_gordon_setter_canine_hereditary_ataxia_dogGordon Setter — Canine hereditary ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_gordon_setter_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogGordon Setter — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_gordon_setter_omia3601_dogGordon Setter — Neurological syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_gordon_setter_progressive_retinal_atrophy_dogGordon Setter — progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_gotland_pony_horse_omia3790_horseGotland Pony (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_grand_basset_griffon_vendeen_omia1271_dogGrand Basset Griffon Vendeen — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_grand_basset_griffon_vendeen_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogGrand Basset Griffon Vendeen — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_congenital_idiopathic_megaesophagus_dogGreat Dane — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_dilated_cardiomyopathy_dogGreat Dane — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_mps_vi_dogGreat Dane — MPS VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_omia1373_dogGreat Dane — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_omia2053_dogGreat Dane — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_omia340_dogGreat Dane — Central core myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_omia3791_dogGreat Dane — Ichthyosis, SLC27A4-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_omia4432_dogGreat Dane — Laryngeal paralysis and polyneuropathy, CNTNAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_dane_this_is_the_classic_m_merle_locus_little_1957_dogGreat Dane — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_pyrenees_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogGreat Pyrenees — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_pyrenees_canine_multifocal_retinopathy_dogGreat Pyrenees — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_pyrenees_dew_claws_canine_preaxial_polydactyly_dogGreat Pyrenees — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_pyrenees_omia1373_dogGreat Pyrenees — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_pyrenees_omia372_dogGreat Pyrenees — Chondrodysplasia, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_pyrenees_omia5640_dogGreat Pyrenees — Ataxia, spastic, SACS-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_pyrenees_omia650_dogGreat Pyrenees — Factor XI deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_great_pyrenees_procoagulant_expression_canine_platelet_procoagulant_deficie_dogGreat Pyrenees — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_greater_swiss_mountain_dog_adp_response_impaired_postoperative_haemorrhage_hemorrhage_g_dogGreater Swiss Mountain Dog — Bleeding disorder, P2RY12-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_greyhound_hereditary_nasal_parakeratosis_dogGreyhound — Hereditary nasal parakeratosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_greyhound_omia1191_dogGreyhound — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_greyhound_omia3512_dogGreyhound — Amelogenesis imperfecta, ENAM-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_greyhound_omia4052_dogGreyhound — Polyneuropathy, NDRG1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_greyhound_omia4152_dogGreyhound — Bald thigh syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_greyhound_omia6106_dogGreyhound — Drug metabolism, altered (hereditary; OMIA-verified breed predisposition)companion_breed_health_haflinger_horse_equine_rhabdomyolysis_syndrome_polysaccharide_storage_myopat_horseHaflinger (Horse) — Equine rhabdomyolysis syndrome; Polysaccharide storage myopathy; Tying-up (hereditary; OMIA-verified breed predisposition)companion_breed_health_haflinger_horse_omia2113_horseHaflinger (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_haflinger_horse_omia2177_horseHaflinger (Horse) — Ocular squamous cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_haflinger_horse_tobiano_sabino_horseHaflinger (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_harrier_omia2648_dogHarrier — Hypocatalasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_harrier_omia647_dogHarrier — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_havana_late_onset_photoreceptor_degeneration_catHavana — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_havanna_rabbit_omia2943_rabbitHavanna (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_havanna_rabbit_omia3848_rabbitHavanna (Rabbit) — Coat colour, brown, TYRP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_heideterrier_jack_russel_terrier_type_congenital_myasthenic_syndrome_post_dogHeideterrier — Myasthenic syndrome, congenital, CHRNE-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_highland_fold_scottish_fold_scottish_fold_osteochondrodysplasia_sfocd_oste_catHighland Fold — Scottish fold, Scottish Fold osteochondrodysplasia (SFOCD), osteodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_feline_familial_hcm_6367_catHighlander — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_feline_familial_hcm_catHighlander — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_inherited_retinal_dystrophic_or_degenerative_disorders_early_catHighlander — Retinal atrophy, progressive, KIF3B-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_late_onset_photoreceptor_degeneration_catHighlander — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_omia2795_catHighlander — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_omia4605_catHighlander — Spinal muscular atrophy, LIX1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_omia652_catHighlander — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_shorthair_inherited_retinal_dystrophic_or_degenerative_disorders_early_catHighlander Shorthair — Retinal atrophy, progressive, KIF3B-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_highlander_shorthair_omia2795_catHighlander Shorthair — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_himalayan_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catHimalayan — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_himalayan_omia1487_catHimalayan — Hyperoxaluria, primary, type II (Oxalosis II) (hereditary; OMIA-verified breed predisposition)companion_breed_health_himalayan_omia37_catHimalayan — Dermatosparaxis Ehlers-Danlos syndrome (dEDS), ADAMTS2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_himalayan_omia3818_catHimalayan — Brachycephaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_himalayan_omia652_catHimalayan — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_himalayan_omia681_catHimalayan — Fibrodysplasia ossificans (hereditary; OMIA-verified breed predisposition)companion_breed_health_hokkaido_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogHokkaido — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_holland_lop_rabbit_omia554_rabbitHolland Lop (Rabbit) — Dwarfism, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_holsteiner_horse_tobiano_sabino_horseHolsteiner (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_hovawart_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogHovawart — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_hovawart_omia54_dogHovawart — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogHuntaway — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogHuntaway — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_copper_toxicosis_copper_storage_disease_copper_associated_he_dogHuntaway — Wilson disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_dew_claws_canine_preaxial_polydactyly_dogHuntaway — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogHuntaway — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_ivermectin_sensitivity_dogHuntaway — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_omia2817_dogHuntaway — Trapped Neutrophil Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_omia2977_dogHuntaway — Neuronal ceroid lipofuscinosis, 8 (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_omia3009_dogHuntaway — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_protein_deletion_dogHuntaway — Protein deletion (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogHuntaway — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_huntaway_this_is_the_classic_b_brown_locus_described_by_little_1957_dogHuntaway — This is the classic B (Brown) locus described by Little (1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_ibizan_hound_canine_multiple_system_degeneration_striatonigral_and_cerebe_dogIbizan Hound — Multiple system degeneration, SERAC1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_chestnut_horseIcelandic Horse (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_equine_multiple_congenital_ocular_anomalies_previously_known_horseIcelandic Horse (Horse) — Multiple ocular defects (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_omia2313_horseIcelandic Horse (Horse) — Cerebellar abiotrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_omia3380_horseIcelandic Horse (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_omia3790_horseIcelandic Horse (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_omia4373_horseIcelandic Horse (Horse) — Coat colour, albinism, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_silver_dapple_horseIcelandic Horse (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_splashed_white_macchiato_horseIcelandic Horse (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_icelandic_horse_horse_tobiano_sabino_horseIcelandic Horse (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_red_and_white_setter_canine_leukocyte_adhesion_deficiency_dogIrish Red and White Setter — Canine leukocyte adhesion deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogIrish Setter — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_canine_leukocyte_adhesion_deficiency_dogIrish Setter — Canine leukocyte adhesion deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_classical_haemophilia_hemophilia_dogIrish Setter — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_congenital_idiopathic_megaesophagus_dogIrish Setter — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_globoid_cell_leukodystrophy_dogIrish Setter — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_omia1311_dogIrish Setter — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_omia1373_dogIrish Setter — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_omia5594_dogIrish Setter — Lissencephaly, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_setter_progressive_retinal_atrophy_dogIrish Setter — progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_terrier_also_described_as_epidermal_acantholysis_dogIrish Terrier — Also described as epidermal acantholysis (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_terrier_cystine_urolithiasis_dogIrish Terrier — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_terrier_hereditary_footpad_hyperkeratosis_dogIrish Terrier — Hereditary Footpad Hyperkeratosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_terrier_omia1271_dogIrish Terrier — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_terrier_omia3009_dogIrish Terrier — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_terrier_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogIrish Terrier — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_water_spaniel_omia647_dogIrish Water Spaniel — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_wolfhound_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogIrish Wolfhound — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_wolfhound_dilated_cardiomyopathy_dogIrish Wolfhound — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_wolfhound_omia1373_dogIrish Wolfhound — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_wolfhound_omia3122_dogIrish Wolfhound — Hyperekplexia (Startle disease), SLC6A5-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_irish_wolfhound_omia655_dogIrish Wolfhound — Fanconi syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_cane_corso_canine_multifocal_retinopathy_dogItalian Cane Corso — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_cane_corso_omia2974_dogItalian Cane Corso — Neuronal ceroid lipofuscinosis, 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_cane_corso_omia4768_dogItalian Cane Corso — Dental-skeletal-retinal anomaly, MIA3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_cane_corso_ridge_hair_ridge_dermoid_cyst_dogItalian Cane Corso — ridge; hair ridge; dermoid cyst (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_greyhound_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogItalian Greyhound — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_greyhound_omia3521_dogItalian Greyhound — Multiple autoimmune diseases syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_greyhound_omia4642_dogItalian Greyhound — Vitreous degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_greyhound_omia4759_dogItalian Greyhound — Congenital muscular dystrophy, LAMA2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_hound_omia3893_dogItalian Hound — Myeloperoxidase deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_italian_spinone_spinocerebellar_ataxia_dogItalian Spinone — Spinocerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_bob_tail_bob_tail_dogJack Russell Terrier — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogJack Russell Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogJack Russell Terrier — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogJack Russell Terrier — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_combined_immunodeficiency_disease_2674_dogJack Russell Terrier — Combined immunodeficiency disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_congenital_sensorineural_deafness_dogJack Russell Terrier — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_jack_russel_terrier_type_congenital_myasthenic_syndrome_post_dogJack Russell Terrier — Myasthenic syndrome, congenital, CHRNE-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_omia2053_dogJack Russell Terrier — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_omia4347_dogJack Russell Terrier — Familial adenomatous polyposis (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_omia54_dogJack Russell Terrier — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_omia6861_dogJack Russell Terrier — Ataxia, SETX-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogJack Russell Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_spinocerebellar_ataxia_hereditary_ataxia_dogJack Russell Terrier — spinocerebellar ataxia, hereditary ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogJack Russell Terrier — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogJack Russell Terrier — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_jack_russell_terrier_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogJack Russell Terrier — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_japanese_bobtail_bobtail_bobbed_tail_catJapanese Bobtail — Bobtail, bobbed tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_japanese_chin_gangliosidosis_gm2_type_i_dogJapanese Chin — Gangliosidosis, GM2, type I (hereditary; OMIA-verified breed predisposition)companion_breed_health_japanese_domestic_omia2877_catJapanese Domestic — Gangliosidosis, GM2, type II (Sandhoff or variant 0) (hereditary; OMIA-verified breed predisposition)companion_breed_health_japanese_domestic_omia3956_catJapanese Domestic — Niemann-Pick disease, type C2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_japanese_draft_japan_horse_tobiano_sabino_horseJapanese Draft, Japan (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_japanese_rabbit_omia2902_rabbitJapanese (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_japanese_spitz_omia647_dogJapanese Spitz — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_japanese_spitz_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogJapanese Spitz — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_karelian_bear_dog_bob_tail_bob_tail_dogKarelian Bear Dog — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_karelian_bear_dog_combined_pituitary_hormone_deficiency_dwarfism_hypopituitari_4465_dogKarelian Bear Dog — Pituitary hormone deficiency, POU1F1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_karelian_bear_dog_omia2489_dogKarelian Bear Dog — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_karelian_bear_dog_omia3653_dogKarelian Bear Dog — Chondrodysplasia, disproportionate short-limbed, ITGA10-related' (hereditary; OMIA-verified breed predisposition)companion_breed_health_karelian_bear_dog_omia4144_dogKarelian Bear Dog — Hypophosphatasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_karelian_bear_dog_omia569_dogKarelian Bear Dog — Pituitary hormone deficiency, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_keeshond_omia1723_dogKeeshond — Tetralogy of Fallot (hereditary; OMIA-verified breed predisposition)companion_breed_health_keeshond_omia451_dogKeeshond — Conotruncal heart malformations (hereditary; OMIA-verified breed predisposition)companion_breed_health_keeshond_this_entry_includes_information_about_primary_hyperparathyro_dogKeeshond — This entry includes information about primary hyperparathyroidism (PHPT) (hereditary; OMIA-verified breed predisposition)companion_breed_health_kentucky_mountain_saddle_united_states_of_america_horse_equine_multiple_congenital_ocular_anomalies_previously_known_horseKentucky Mountain Saddle, United States of America (Horse) — Multiple ocular defects (hereditary; OMIA-verified breed predisposition)companion_breed_health_kentucky_mountain_saddle_united_states_of_america_horse_omia3380_horseKentucky Mountain Saddle, United States of America (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_kerry_blue_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogKerry Blue Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_kerry_blue_terrier_canine_multiple_system_degeneration_striatonigral_and_cerebe_dogKerry Blue Terrier — Multiple system degeneration, SERAC1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_kerry_blue_terrier_cerebellar_ataxia_dogKerry Blue Terrier — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_kerry_blue_terrier_omia650_dogKerry Blue Terrier — Factor XI deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_kerry_blue_terrier_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogKerry Blue Terrier — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_king_charles_spaniel_the_disease_is_also_called_arnold_chiari_malformation_caudal_dogKing Charles Spaniel — Chiari malformation Type I with syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_kinkalow_x_linked_muscular_dystrophy_catKinkalow — X-linked muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_knabstrupper_horse_omia4086_horseKnabstrupper (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_komondor_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogKomondor — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_komondor_omia3472_dogKomondor — Intestinal cobalamin (vitamin B12) malabsorption, CUBN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_komondor_omia957_dogKomondor — Intestinal cobalamin malabsorption, AMN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_koolie_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogKoolie — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_korat_atherosclerosis_catKorat — atherosclerosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_korat_omia2877_catKorat — Gangliosidosis, GM2, type II (Sandhoff or variant 0) (hereditary; OMIA-verified breed predisposition)companion_breed_health_kromfohrlander_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogKromfohrlander — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_kromfohrlander_hereditary_footpad_hyperkeratosis_dogKromfohrlander — Hereditary Footpad Hyperkeratosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_kurilian_bobtail_manx_tailllessness_catKurilian Bobtail — Manx tailllessness (hereditary; OMIA-verified breed predisposition)companion_breed_health_kuvasz_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogKuvasz — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_kuvasz_omia1373_dogKuvasz — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_kuvasz_omia2489_dogKuvasz — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labradoodle_omia2489_dogLabradoodle — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labradoodle_this_is_the_classic_m_merle_locus_little_1957_dogLabradoodle — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_canine_atopic_dermatitis_cad_dogLabrador Retriever — Canine atopic dermatitis (CAD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogLabrador Retriever — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_cerebellar_ataxia_dogLabrador Retriever — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__dogLabrador Retriever — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_classical_haemophilia_hemophilia_dogLabrador Retriever — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_congenital_idiopathic_megaesophagus_dogLabrador Retriever — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_congenital_myasthenic_syndromes_dogLabrador Retriever — Congenital myasthenic syndromes (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_copper_toxicosis_copper_storage_disease_copper_associated_he_dogLabrador Retriever — Wilson disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_cystine_urolithiasis_dogLabrador Retriever — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogLabrador Retriever — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_epidermolytic_hyperkeratosis_epidermolytic_ichthyosis_dogLabrador Retriever — Epidermolytic hyperkeratosis; epidermolytic ichthyosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_fibrinoid_leukodystrophy_fibrinoid_encephalomyelopathy_dogLabrador Retriever — Fibrinoid leukodystrophy, fibrinoid encephalomyelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_hereditary_nasal_parakeratosis_dogLabrador Retriever — Hereditary nasal parakeratosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_hip_dysplasia_dogLabrador Retriever — Hip Dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_hyperuricosuria_and_hyperuricemia_dogLabrador Retriever — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_lethal_brachycephalic_like_facial_dysmorphia_dogLabrador Retriever — lethal brachycephalic-like facial dysmorphia (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_many_alias_names_exist_for_the_phenotype_they_include_congen_dogLabrador Retriever — Many alias names exist for the phenotype. They include congenital cornification disorder; CHILD nevi; CHILD-like nevi; ILVEN. The human phenotype resulting from NSDHL loss-of-function variants is termed congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD syndrome). CHILD syndrome is characterized by epidermal nevi and striking unilateral limb defects. Animals (dogs, cats, mice) with NSDHL variants have similar epidermal nevi, but so far were never reported to also have the limb defects seen in human CHILD syndrome. (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia1191_dogLabrador Retriever — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia1271_dogLabrador Retriever — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia1311_dogLabrador Retriever — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia1373_dogLabrador Retriever — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia1515_dogLabrador Retriever — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia2053_dogLabrador Retriever — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia2489_dogLabrador Retriever — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia2885_dogLabrador Retriever — Exercise-induced collapse (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia2996_dogLabrador Retriever — Oculoskeletal dysplasia 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia3869_dogLabrador Retriever — Obesity (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia3969_dogLabrador Retriever — Macular corneal dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia4296_dogLabrador Retriever — Calvarial hyperostotic syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia4432_dogLabrador Retriever — Laryngeal paralysis and polyneuropathy, CNTNAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia4760_dogLabrador Retriever — Muscular dystrophy-dystroglycanopathy, LARGE1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia4980_dogLabrador Retriever — Dyserythropoietic anemia and myopathy syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia54_dogLabrador Retriever — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia6271_dogLabrador Retriever — Retinal atrophy, progressive, GTPBP2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_omia6783_dogLabrador Retriever — Paw pad hyperkeratosis, GJB6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_procoagulant_expression_canine_platelet_procoagulant_deficie_dogLabrador Retriever — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_retinal_atrophy_generalized_retinal_atrophy_abca4_related_dogLabrador Retriever — Retinal atrophy - generalized; retinal atrophy, ABCA4-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_skeletal_dysplasia_2_dogLabrador Retriever — Skeletal dysplasia 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_this_entry_was_previously_called_ichthyosis_golden_retriever_dogLabrador Retriever — This entry was previously called Ichthyosis, Golden Retriever (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_type_ii_fiber_deficiency_autosomal_recessive_muscular_dystro_dogLabrador Retriever — Centronuclear myopathy, HACD1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_ullrich_like_congenital_muscular_dystrophy_sarcolemmal_speci_dogLabrador Retriever — Muscular dystrophy, Ullrich type, COL6A3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_labrador_retriever_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogLabrador Retriever — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_lagotto_romagnolo_autosomal_dominant_polycystic_kidney_disease_adpkd_bull_terr_dogLagotto Romagnolo — Polycystic kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_lagotto_romagnolo_benign_familial_juvenile_epilepsy_remitting_focal_epilepsy_b_dogLagotto Romagnolo — Epilepsy, benign familial juvenile, LGI2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_lagotto_romagnolo_cerebellar_ataxia_dogLagotto Romagnolo — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_lagotto_romagnolo_lagotto_storage_disease_dogLagotto Romagnolo — Lagotto storage disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_lagotto_romagnolo_omia3009_dogLagotto Romagnolo — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_lagotto_romagnolo_omia4053_dogLagotto Romagnolo — Muscular dystrophy, limb-girdle, type R6 (LGMDR6) (hereditary; OMIA-verified breed predisposition)companion_breed_health_lagotto_romagnolo_omia458_dogLagotto Romagnolo — Corneal dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_lagotto_romagnolo_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogLagotto Romagnolo — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_lancashire_heeler_charcot_marie_tooth_disease_1j_with_amelogenesis_imperfecta_dogLancashire Heeler — Charcot-Marie-Tooth disease 1J with amelogenesis imperfecta (hereditary; OMIA-verified breed predisposition)companion_breed_health_lancashire_heeler_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogLancashire Heeler — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_lancashire_heeler_omia4947_dogLancashire Heeler — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_lancashire_heeler_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogLancashire Heeler — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_lancashire_heeler_this_is_the_classic_b_brown_locus_described_by_little_1957_dogLancashire Heeler — This is the classic B (Brown) locus described by Little (1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_landseer_caldag_gefi_thrombopathia_caldag_gefi_platelet_disorder_dogLandseer — CalDAG-GEFI thrombopathia; CalDAG-GEFI platelet disorder (hereditary; OMIA-verified breed predisposition)companion_breed_health_landseer_cystine_urolithiasis_dogLandseer — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_landseer_muscular_dystrophy_dogLandseer — Muscular Dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_laperm_omia2795_catLaPerm — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_lapponian_herder_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogLapponian Herder — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_lapponian_herder_omia2489_dogLapponian Herder — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_lapponian_herder_omia3066_dogLapponian Herder — Multifocal retinopathy 3 (hereditary; OMIA-verified breed predisposition)companion_breed_health_lapponian_herder_omia4473_dogLapponian Herder — Retinal atrophy, progressive, IFT122-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_lapponian_herder_omia726_dogLapponian Herder — Glycogen storage disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_large_munsterlander_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogLarge Munsterlander — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_large_munsterlander_hyperuricosuria_and_hyperuricemia_dogLarge Munsterlander — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_leonberger_omia1785_dogLeonberger — Ventricular arrhythmias and sudden death (hereditary; OMIA-verified breed predisposition)companion_breed_health_leonberger_omia1851_dogLeonberger — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_leonberger_omia1978_dogLeonberger — Polyglandular autoimmune syndrome, type II (hereditary; OMIA-verified breed predisposition)companion_breed_health_leonberger_omia4050_dogLeonberger — Polyneuropathy, GJA9-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_leonberger_omia4432_dogLeonberger — Laryngeal paralysis and polyneuropathy, CNTNAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_leonberger_polyneuropathy_dogLeonberger — polyneuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_leonberger_this_is_the_classic_b_brown_locus_described_by_little_1957_dogLeonberger — This is the classic B (Brown) locus described by Little (1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_lhasa_apso_hyperuricosuria_and_hyperuricemia_dogLhasa Apso — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_lhasa_apso_omia54_dogLhasa Apso — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_lhasa_apso_omia5594_dogLhasa Apso — Lissencephaly, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_lhasa_apso_progressive_retinal_atrophy_4_dogLhasa Apso — Progressive retinal atrophy 4 (hereditary; OMIA-verified breed predisposition)companion_breed_health_lhasa_apso_white_doberman_pinscher_dogLhasa Apso — White Doberman Pinscher (hereditary; OMIA-verified breed predisposition)companion_breed_health_lionhead_dwarf_omia5954_rabbitLionhead Dwarf — Neuronal ceroid lipofuscinosis, 7 (hereditary; OMIA-verified breed predisposition)companion_breed_health_lipizzan_horse_horse_splashed_white_horseLipizzan horse (Horse) — splashed white (hereditary; OMIA-verified breed predisposition)companion_breed_health_lipizzan_horse_horse_tobiano_sabino_horseLipizzan horse (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_long_haired_whippet_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogLong-Haired Whippet — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_long_haired_whippet_ivermectin_sensitivity_dogLong-Haired Whippet — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_lop_dwarf_omia2902_rabbitLop dwarf — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_lop_dwarf_omia2943_rabbitLop dwarf — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_lop_omia2902_rabbitLop — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_lop_omia2943_rabbitLop — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_lundehund_dew_claws_canine_preaxial_polydactyly_dogLundehund — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_lundehund_omia3896_dogLundehund — Lundehund syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_lusitanian_horse_omia2113_horseLusitanian (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_lusitanian_horse_palomino_horseLusitanian (Horse) — Palomino (hereditary; OMIA-verified breed predisposition)companion_breed_health_lykoi_omia2795_catLykoi — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_lykoi_omia652_catLykoi — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_magyar_ag_r_omia4152_dogMagyar Agár — Bald thigh syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catMaine Coon — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__catMaine Coon — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related; Ehlers-Danlos syndrome, classic type, 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_dominant_blue_eyes_dbe_catMaine Coon — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_feline_familial_hcm_6368_catMaine Coon — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_feline_familial_hcm_catMaine Coon — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_hereditary_factor_xi_deficiency_congenital_factor_xi_deficie_catMaine Coon — Hereditary factor XI deficiency; congenital factor XI deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_late_onset_photoreceptor_degeneration_catMaine Coon — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_omia1459_catMaine Coon — Polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_omia2795_catMaine Coon — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_omia3786_catMaine Coon — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_omia4436_catMaine Coon — Cardiomyopathy, hypertrophic, TNNT2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_omia4605_catMaine Coon — Spinal muscular atrophy, LIX1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_omia652_catMaine Coon — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_omia681_catMaine Coon — Fibrodysplasia ossificans (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_polydactyl_feline_familial_hcm_881_catMaine Coon Polydactyl — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_polydactyl_feline_familial_hcm_catMaine Coon Polydactyl — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_polydactyl_omia2795_catMaine Coon Polydactyl — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_polydactyl_omia3786_catMaine Coon Polydactyl — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_polydactyl_omia4605_catMaine Coon Polydactyl — Spinal muscular atrophy, LIX1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_polydactyl_omia652_catMaine Coon Polydactyl — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_maine_coon_x_linked_muscular_dystrophy_catMaine Coon — X-linked muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_majorca_mastiff_hyperuricosuria_and_hyperuricemia_dogMajorca Mastiff — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_malopolski_horse_omia4086_horseMalopolski (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_maltese_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__dogMaltese — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related; Ehlers-Danlos syndrome, classic type, 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_maltese_omia3879_dogMaltese — Ligneous membranitis (hereditary; OMIA-verified breed predisposition)companion_breed_health_maltese_persistent_m_llerian_duct_syndrome_dogMaltese — Persistent Müllerian Duct Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_maltese_terrier_omia54_dogMaltese Terrier — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_maltese_terrier_omia723_dogMaltese Terrier — Glycogen storage disease Ia (hereditary; OMIA-verified breed predisposition)companion_breed_health_manchester_terrier_sudden_cardiac_death_in_the_young_scdy_and_dilated_cardiomyo_dogManchester Terrier — Sudden cardiac death in the young (SCDY) and dilated cardiomyopathy (DCM) (hereditary; OMIA-verified breed predisposition)companion_breed_health_manchester_terrier_xanthine_urolithiasis_xanthine_nephrolithiasis_dogManchester Terrier — Xanthine urolithiasis; xanthine nephrolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_manx_late_onset_photoreceptor_degeneration_catManx — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_manx_manx_tailllessness_catManx — Manx tailllessness (hereditary; OMIA-verified breed predisposition)companion_breed_health_manx_omia652_catManx — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_marburger_feh_rabbit_omia2943_rabbitMarburger Feh (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_mastiff_cystine_urolithiasis_dogMastiff — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_mcnab_shepherd_ivermectin_sensitivity_dogMcNab Shepherd — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_mini_silver_omia2943_rabbitMini Silver — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_american_shepherd_omia6067_dogMiniature American Shepherd — Neuroaxonal dystrophy, RNF170-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_american_shepherd_this_is_the_classic_b_brown_locus_described_by_little_1957_dogMiniature American Shepherd — This is the classic B (Brown) locus described by Little (1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_american_shepherd_this_is_the_classic_m_merle_locus_little_1957_dogMiniature American Shepherd — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_australian_shepherd_dog_ivermectin_sensitivity_dogMiniature Australian Shepherd Dog — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_australian_shepherd_dog_omia5367_dogMiniature Australian Shepherd Dog — Hyperekplexia, GLRA1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_australian_shepherd_dog_this_is_the_classic_m_merle_locus_little_1957_dogMiniature Australian Shepherd Dog — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_bull_terrier_lethal_acrodermatitis_dogMiniature Bull Terrier — Lethal acrodermatitis (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_bull_terrier_omia4251_dogMiniature Bull Terrier — Laryngeal paralysis, RAPGEF6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_bull_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogMiniature Bull Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_horse_horse_omia3715_horseMiniature Horse (Horse) — Dwarfism, ACAN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_horse_horse_omia5331_horseMiniature Horse (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_horse_horse_overo_lethal_white_foal_syndrome_frame_overo_spotting_horseMiniature Horse (Horse) — Overo lethal white foal syndrome; frame overo spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_horse_horse_tobiano_sabino_horseMiniature Horse (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_pinscher_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogMiniature Pinscher — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_pinscher_cystine_urolithiasis_dogMiniature Pinscher — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_pinscher_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogMiniature Pinscher — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_pinscher_hereditary_sensory_neuropathy_dogMiniature Pinscher — hereditary sensory neuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_pinscher_mps_vi_dogMiniature Pinscher — MPS VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_pinscher_primary_hereditary_cataract_dogMiniature Pinscher — Primary hereditary cataract (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_classical_haemophilia_hemophilia_dogMiniature Schnauzer — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_congenital_idiopathic_megaesophagus_dogMiniature Schnauzer — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_hyperuricosuria_and_hyperuricemia_dogMiniature Schnauzer — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_mps_vi_dogMiniature Schnauzer — MPS VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_omia1188_dogMiniature Schnauzer — Histiocytosis, malignant (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_omia1271_dogMiniature Schnauzer — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_omia1515_dogMiniature Schnauzer — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_omia2053_dogMiniature Schnauzer — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_omia2998_dogMiniature Schnauzer — Gallbladder mucoceles (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_omia3748_dogMiniature Schnauzer — Spondylocostal dysostosis, autosomal recessive (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_omia4395_dogMiniature Schnauzer — Polyneuropathy, SBF2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_omia647_dogMiniature Schnauzer — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_persistent_m_llerian_duct_syndrome_dogMiniature Schnauzer — Persistent Müllerian Duct Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_progressive_retinal_atrophy_type_1_dogMiniature Schnauzer — Progressive retinal atrophy, type 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_miniature_schnauzer_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogMiniature Schnauzer — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_minuet_longhair_omia2795_catMinuet Longhair — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_minuet_longhair_omia652_catMinuet Longhair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_minuet_omia652_catMinuet — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_minuet_scottish_fold_scottish_fold_osteochondrodysplasia_sfocd_oste_catMinuet — Scottish fold, Scottish Fold osteochondrodysplasia (SFOCD), osteodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_missouri_fox_trotter_germany_horse_equine_multiple_congenital_ocular_anomalies_previously_known_horseMissouri Fox Trotter, Germany (Horse) — Multiple ocular defects (hereditary; OMIA-verified breed predisposition)companion_breed_health_missouri_fox_trotter_germany_horse_silver_dapple_horseMissouri Fox Trotter, Germany (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_missouri_fox_trotting_horse_horse_omia3380_horseMissouri Fox Trotting Horse (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_missouri_fox_trotting_horse_horse_omia483_horseMissouri Fox Trotting Horse (Horse) — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_missouri_fox_trotting_horse_united_states_of_america_horse_omia5331_horseMissouri Fox Trotting Horse, United States of America (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_acromelanism_himalayan_coat_color_colour_dogMixed Breed — Acromelanism; Himalayan coat color/colour (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_canine_hereditary_ataxia_dogMixed Breed — Canine hereditary ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_canine_leukocyte_adhesion_deficiency_dogMixed Breed — Canine leukocyte adhesion deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_canine_multiple_system_degeneration_striatonigral_and_cerebe_dogMixed Breed — Multiple system degeneration, SERAC1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_classic_like_ehlers_danlos_syndrome_cleds_tnxb_related_ehler_dogMixed Breed — classic-like Ehlers-Danlos syndrome (clEDS), TNXB-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__dogMixed Breed — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related; Ehlers-Danlos syndrome, classic type, 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_congenital_insensitivity_to_pain_dogMixed Breed — Congenital insensitivity to pain (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogMixed Breed — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_fxiii_dogMixed Breed — FXIII (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_globoid_cell_leukodystrophy_dogMixed Breed — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_granuloprival_cerebellar_cortical_degeneration_dogMixed Breed — Granuloprival cerebellar cortical degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_grey_collie_syndrome_gray_collie_syndrome_dogMixed Breed — Grey Collie Syndrome; Gray Collie Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_ivermectin_sensitivity_dogMixed Breed — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_many_alias_names_exist_for_the_phenotype_they_include_congen_dogMixed Breed — Many alias names exist for the phenotype. They include congenital cornification disorder; CHILD nevi; CHILD-like nevi; ILVEN. The human phenotype resulting from NSDHL loss-of-function variants is termed congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD syndrome). CHILD syndrome is characterized by epidermal nevi and striking unilateral limb defects. Animals (dogs, cats, mice) with NSDHL variants have similar epidermal nevi, but so far were never reported to also have the limb defects seen in human CHILD syndrome. (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogMixed Breed — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia1191_dogMixed Breed — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia1311_dogMixed Breed — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia1422_dogMixed Breed — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia2053_dogMixed Breed — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia2992_dogMixed Breed — Retinal atrophy, progressive, X-linked, type 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia3364_dogMixed Breed — Gangliosidosis, GM2, type II (Sandhoff or variant 0) (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia4184_dogMixed Breed — Mannosidosis, beta (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia4312_dogMixed Breed — Glucocorticoid resistance (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia4406_dogMixed Breed — Glycogen storage disease IV (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia4736_dogMixed Breed — Xanthinuria, type I (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia54_dogMixed Breed — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia5594_dogMixed Breed — Lissencephaly, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia5908_dogMixed Breed — Leigh syndrome, NDUFS7-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia647_dogMixed Breed — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia6857_dogMixed Breed — Myopathy, creatine deficiency disorder, GATM-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_omia6871_dogMixed Breed — Phloiokeratosis, SUV39H1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_renal_cancer_syndrome_nodular_dermatofibrosis_and_kidney_dis_dogMixed Breed — Renal cancer syndrome, nodular dermatofibrosis and kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_mixed_breed_sensory_neuropathy_hereditary_sensory_and_autonomic_neuropat_dogMixed Breed — Sensory neuropathy; hereditary sensory and autonomic neuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_mongolian_horse_omia3790_horseMongolian (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_morgan_horse_chestnut_horseMorgan (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_morgan_horse_omia2113_horseMorgan (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_morgan_horse_omia3380_horseMorgan (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_morgan_horse_omia5331_horseMorgan (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_morgan_horse_palomino_horseMorgan (Horse) — Palomino (hereditary; OMIA-verified breed predisposition)companion_breed_health_morgan_horse_silver_dapple_horseMorgan (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_morgan_horse_splashed_white_macchiato_horseMorgan (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_morgan_horse_tobiano_sabino_horseMorgan (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_mudi_bob_tail_bob_tail_dogMudi — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_mudi_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogMudi — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_mudi_this_is_the_classic_m_merle_locus_little_1957_dogMudi — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_feline_familial_hcm_6368_catMunchkin — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_feline_familial_hcm_881_catMunchkin — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_feline_familial_hcm_catMunchkin — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_late_onset_photoreceptor_degeneration_catMunchkin — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_longhair_omia652_catMunchkin Longhair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_omia2795_catMunchkin — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_omia4466_catMunchkin — Cardiomyopathy, hypertrophic, ALMS1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_omia4946_catMunchkin — Chondrodysplasia, UGDH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_omia652_catMunchkin — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_munchkin_scottish_fold_scottish_fold_osteochondrodysplasia_sfocd_oste_catMunchkin — Scottish fold, Scottish Fold osteochondrodysplasia (SFOCD), osteodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_navasota_mixed_breed_alport_syndrome_x_linked_hereditary_nephropathy_glomerulonep_dogNavasota (mixed breed) — Nephritis, X-linked (hereditary; OMIA-verified breed predisposition)companion_breed_health_nederlandse_kooikerhondje_hereditary_necrotizing_myelopathy_dogNederlandse Kooikerhondje — Hereditary necrotizing myelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_nederlandse_kooikerhondje_omia1851_dogNederlandse Kooikerhondje — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_nederlandse_kooikerhondje_omia3634_dogNederlandse Kooikerhondje — Polymyositis (hereditary; OMIA-verified breed predisposition)companion_breed_health_netherland_dwarf_rabbit_omia554_rabbitNetherland dwarf (Rabbit) — Dwarfism, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_neva_masquerade_omia2795_catNeva Masquerade — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_neva_masquerade_omia652_catNeva Masquerade — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_forest_pony_horse_omia3326_horseNew Forest Pony (Horse) — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogNew Zealand Heading Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogNew Zealand Heading Dog — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_copper_toxicosis_copper_storage_disease_copper_associated_he_dogNew Zealand Heading Dog — Wilson disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_dew_claws_canine_preaxial_polydactyly_dogNew Zealand Heading Dog — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_ivermectin_sensitivity_dogNew Zealand Heading Dog — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_omia2817_dogNew Zealand Heading Dog — Trapped Neutrophil Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_omia2977_dogNew Zealand Heading Dog — Neuronal ceroid lipofuscinosis, 8 (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_omia3009_dogNew Zealand Heading Dog — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_omia3472_dogNew Zealand Heading Dog — Intestinal cobalamin (vitamin B12) malabsorption, CUBN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_omia3896_dogNew Zealand Heading Dog — Lundehund syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_omia4432_dogNew Zealand Heading Dog — Laryngeal paralysis and polyneuropathy, CNTNAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_protein_deletion_dogNew Zealand Heading Dog — Protein deletion (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogNew Zealand Heading Dog — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_heading_dog_this_is_the_classic_b_brown_locus_described_by_little_1957_dogNew Zealand Heading Dog — This is the classic B (Brown) locus described by Little (1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_red_rabbit_omia2902_rabbitNew Zealand Red (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_white_rabbit_omia2841_rabbitNew Zealand White (Rabbit) — Yellow fat (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_white_rabbit_omia2902_rabbitNew Zealand White (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_white_rabbit_omia2943_rabbitNew Zealand White (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_white_rabbit_omia423_rabbitNew Zealand White (Rabbit) — Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_white_rabbit_omia5073_rabbitNew Zealand White (Rabbit) — Amelogenesis imperfecta, FAM83H-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_new_zealand_white_rabbit_omia6041_rabbitNew Zealand White (Rabbit) — Cerebral palsy, RHOB-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_newfoundland_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogNewfoundland — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_newfoundland_congenital_idiopathic_megaesophagus_dogNewfoundland — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_newfoundland_cystine_urolithiasis_dogNewfoundland — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_newfoundland_dilated_cardiomyopathy_dogNewfoundland — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_newfoundland_omia1293_dogNewfoundland — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_newfoundland_omia1373_dogNewfoundland — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_newfoundland_omia54_dogNewfoundland — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_norfolk_terrier_epidermolytic_hyperkeratosis_epidermolytic_ichthyosis_dogNorfolk Terrier — Epidermolytic hyperkeratosis; epidermolytic ichthyosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_noric_horse_equine_rhabdomyolysis_syndrome_polysaccharide_storage_myopat_horseNoric (Horse) — Equine rhabdomyolysis syndrome; Polysaccharide storage myopathy; Tying-up (hereditary; OMIA-verified breed predisposition)companion_breed_health_noric_horse_omia2177_horseNoric (Horse) — Ocular squamous cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_noric_horse_omia2497_horseNoric (Horse) — Coat colour, roan (hereditary; OMIA-verified breed predisposition)companion_breed_health_noric_horse_omia4086_horseNoric (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_noric_horse_splashed_white_horseNoric (Horse) — splashed white (hereditary; OMIA-verified breed predisposition)companion_breed_health_noric_horse_tobiano_sabino_horseNoric (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_northern_inuit_dog_omia2996_dogNorthern Inuit Dog — Oculoskeletal dysplasia 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_buhund_progressive_cerebellar_ataxia_dogNorwegian Buhund — Progressive cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_elkhound_omia2489_dogNorwegian Elkhound — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_elkhound_omia3653_dogNorwegian Elkhound — Chondrodysplasia, disproportionate short-limbed, ITGA10-related' (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_elkhound_omia4896_dogNorwegian Elkhound — Ataxia, HACE1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_elkhound_omia655_dogNorwegian Elkhound — Fanconi syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_elkhound_progressive_retinal_atrophy_retinal_atrophy_2_dogNorwegian Elkhound — Progressive retinal atrophy; retinal atrophy -2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_elkhound_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogNorwegian Elkhound — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_forest_cat_feline_familial_hcm_catNorwegian Forest Cat — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_forest_cat_omia2795_catNorwegian Forest Cat — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_forest_cat_omia652_catNorwegian Forest Cat — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_forest_cat_omia728_catNorwegian Forest Cat — Glycogen storage disease IV (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwegian_forest_cat_scottish_fold_scottish_fold_osteochondrodysplasia_sfocd_oste_catNorwegian Forest Cat — Scottish fold, Scottish Fold osteochondrodysplasia (SFOCD), osteodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwich_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogNorwich Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwich_terrier_omia4160_dogNorwich Terrier — Diffuse cystic renal dysplasia and hepatic fibrosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwich_terrier_omia4947_dogNorwich Terrier — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_norwich_terrier_upper_airway_obstructive_syndrome_upper_respiratory_tract_ur_dogNorwich Terrier — upper airway obstructive syndrome; upper respiratory tract (URT) disorder (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogNova Scotia Duck Tolling Retriever — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_cerebellar_degeneration_myositis_complex_inflammatory_myopat_dogNova Scotia Duck Tolling Retriever — Cerebellar degeneration-myositis complex, inflammatory myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogNova Scotia Duck Tolling Retriever — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_dilated_cardiomyopathy_dogNova Scotia Duck Tolling Retriever — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogNova Scotia Duck Tolling Retriever — Intervertebral disc disease, predisposition to (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_omia2489_dogNova Scotia Duck Tolling Retriever — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_omia3941_dogNova Scotia Duck Tolling Retriever — Degenerative encephalopathy, RB1CC1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_omia4076_dogNova Scotia Duck Tolling Retriever — Skeletal dysplasia, FGF4-retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_omia5703_dogNova Scotia Duck Tolling Retriever — Cardiomyopathy, dilated, LMNA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_omia6840_dogNova Scotia Duck Tolling Retriever — Addison’s disease and multiple autoimmune syndrome, RESF1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_orofacial_cleft_palatoschisis_dogNova Scotia Duck Tolling Retriever — orofacial cleft; palatoschisis (hereditary; OMIA-verified breed predisposition)companion_breed_health_nova_scotia_duck_tolling_retriever_palatoschisis_dogNova Scotia Duck Tolling Retriever — Palatoschisis (hereditary; OMIA-verified breed predisposition)companion_breed_health_ocicat_late_onset_photoreceptor_degeneration_catOcicat — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_danish_pointing_dog_congenital_myasthenic_syndrome_dogOld Danish Pointing Dog — Congenital myasthenic syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_danish_pointing_dog_progressive_retinal_atrophy_dogOld Danish Pointing Dog — progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_canine_hereditary_ataxia_dogOld English Sheepdog — Canine hereditary ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_classical_haemophilia_hemophilia_dogOld English Sheepdog — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogOld English Sheepdog — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_ivermectin_sensitivity_dogOld English Sheepdog — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_multiocular_defect_dogOld English Sheepdog — Multiocular defect (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_omia1373_dogOld English Sheepdog — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_omia3122_dogOld English Sheepdog — Hyperekplexia (Startle disease), SLC6A5-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_omia54_dogOld English Sheepdog — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_old_english_sheepdog_primary_ciliary_dyskinesia_dogOld English Sheepdog — Primary ciliary dyskinesia (hereditary; OMIA-verified breed predisposition)companion_breed_health_oldenburg_horse_omia3000_horseOldenburg (Horse) — Thrombasthenia (hereditary; OMIA-verified breed predisposition)companion_breed_health_oldenburg_horse_tobiano_sabino_horseOldenburg (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_oriental_longhair_late_onset_photoreceptor_degeneration_catOriental Longhair — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_oriental_longhair_omia652_catOriental Longhair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_oriental_shorthair_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catOriental Shorthair — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_oriental_shorthair_late_onset_photoreceptor_degeneration_catOriental Shorthair — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_oriental_shorthair_omia2929_catOriental Shorthair — Coat colour, ticked (Abyssinian) (hereditary; OMIA-verified breed predisposition)companion_breed_health_oriental_shorthair_omia652_catOriental Shorthair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_papillon_omia4026_dogPapillon — Neuroaxonal dystrophy, PLA2G6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_papillon_omia5429_dogPapillon — Retinal atrophy, progressive, CNGB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_papillon_omia647_dogPapillon — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_parson_russell_terrier_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogParson Russell Terrier — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_parson_russell_terrier_congenital_idiopathic_megaesophagus_dogParson Russell Terrier — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_parson_russell_terrier_hyperuricosuria_and_hyperuricemia_dogParson Russell Terrier — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_parson_russell_terrier_omia3512_dogParson Russell Terrier — Amelogenesis imperfecta, ENAM-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_parson_russell_terrier_omia4483_dogParson Russell Terrier — Epilepsy, mitochondrial dysfunction and neurodegeneration, PITRM1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_parson_russell_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogParson Russell Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_parson_russell_terrier_spinocerebellar_ataxia_hereditary_ataxia_dogParson Russell Terrier — spinocerebellar ataxia, hereditary ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_parson_russell_terrier_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogParson Russell Terrier — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_paso_fino_horse_omia2113_horsePaso Fino (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_paso_fino_horse_omia3380_horsePaso Fino (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_paso_fino_horse_omia483_horsePaso Fino (Horse) — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_paso_fino_horse_tiger_eye_or_goat_eye_horsePaso Fino (Horse) — Tiger-eye or Goat-eye (hereditary; OMIA-verified breed predisposition)companion_breed_health_patterdale_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogPatterdale Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_pekingese_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogPekingese — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_pekingese_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogPekingese — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_pekingese_hyperuricosuria_and_hyperuricemia_dogPekingese — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_pekingese_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogPekingese — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_pekingese_omia4161_dogPekingese — Hypothyroidism, congenital dyshormonogenic, with goiter, SLC5A5-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_pekingese_omia4947_dogPekingese — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_pekingese_omia5594_dogPekingese — Lissencephaly, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_pekingese_white_doberman_pinscher_dogPekingese — White Doberman Pinscher (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_bob_tail_bob_tail_dogPembroke Welsh Corgi — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogPembroke Welsh Corgi — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogPembroke Welsh Corgi — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_omia1271_dogPembroke Welsh Corgi — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_omia1293_dogPembroke Welsh Corgi — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_omia1311_dogPembroke Welsh Corgi — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_omia2885_dogPembroke Welsh Corgi — Exercise-induced collapse (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_omia3513_dogPembroke Welsh Corgi — Coat colour, saddle tan vs black-and-tan (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_omia4011_dogPembroke Welsh Corgi — Ichthyosis, ASPRV1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_omia4947_dogPembroke Welsh Corgi — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_references_relating_to_chronic_kidney_disease_are_included_i_dogPembroke Welsh Corgi — References relating to chronic kidney disease are included in this entry. (hereditary; OMIA-verified breed predisposition)companion_breed_health_pembroke_welsh_corgi_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogPembroke Welsh Corgi — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_percheron_horse_omia483_horsePercheron (Horse) — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_perro_de_presa_canario_canine_multifocal_retinopathy_dogPerro de Presa Canario — Canine multifocal retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_perro_de_presa_canario_procoagulant_expression_canine_platelet_procoagulant_deficie_dogPerro de Presa Canario — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catPersian — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_dominant_blue_eyes_dbe_catPersian — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_feline_familial_hcm_catPersian — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_omia1199_catPersian — Mannosidosis, alpha (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_omia1487_catPersian — Hyperoxaluria, primary, type II (Oxalosis II) (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_omia364_catPersian — Chediak-Higashi syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_omia3818_catPersian — Brachycephaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_omia652_catPersian — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_persian_x_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catPersian X — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_peruvian_hairless_dog_canine_ectodermal_dysplasia_dogPeruvian Hairless Dog — Canine ectodermal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_peruvian_paso_horse_inherited_myoclonus_horsePeruvian Paso (Horse) — inherited myoclonus (hereditary; OMIA-verified breed predisposition)companion_breed_health_peruvian_paso_horse_omia3380_horsePeruvian Paso (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_peterbald_late_onset_photoreceptor_degeneration_catPeterbald — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_peterbald_omia652_catPeterbald — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_petit_basset_griffon_vendeen_omia4947_dogPetit Basset Griffon Vendeen — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_petit_basset_griffon_vendeen_weill_marchesani_like_syndrome_goniodysgenesis_dogPetit Basset Griffon Vendeen — Weill-Marchesani-like syndrome; goniodysgenesis (hereditary; OMIA-verified breed predisposition)companion_breed_health_petit_brabancon_isolated_growth_hormone_deficiency_dogPetit Brabancon — isolated growth hormone deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_phal_ne_omia5429_dogPhalène — Retinal atrophy, progressive, CNGB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_pixiebob_longhair_feline_familial_hcm_6368_catPixiebob Longhair — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_pixiebob_longhair_feline_familial_hcm_catPixiebob Longhair — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_pixiebob_longhair_late_onset_photoreceptor_degeneration_catPixiebob Longhair — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_pixiebob_longhair_omia2795_catPixiebob Longhair — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_pixiebob_manx_tailllessness_catPixiebob — Manx tailllessness (hereditary; OMIA-verified breed predisposition)companion_breed_health_pixiebob_omia1459_catPixiebob — Polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_pixiebob_omia2795_catPixiebob — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_plott_hound_mucopolysaccharidosis_i_dogPlott Hound — Mucopolysaccharidosis I (hereditary; OMIA-verified breed predisposition)companion_breed_health_podenco_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogPodenco — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_pointer_omia1191_dogPointer — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_pointer_omia1293_dogPointer — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_polish_konik_horse_omia3790_horsePolish Konik (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_polish_lowland_sheepdog_bob_tail_bob_tail_dogPolish Lowland Sheepdog — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_polish_lowland_sheepdog_progressive_retinal_atrophy_dogPolish Lowland Sheepdog — progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_polish_tatra_sheepdog_progressive_retinal_atrophy_dogPolish Tatra Sheepdog — progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_pomeranian_hyperuricosuria_and_hyperuricemia_dogPomeranian — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_pomeranian_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogPomeranian — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_pomeranian_omia2243_dogPomeranian — Syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_pomeranian_omia2926_dogPomeranian — Vitamin D-deficiency rickets, type II (hereditary; OMIA-verified breed predisposition)companion_breed_health_pomeranian_omia2998_dogPomeranian — Gallbladder mucoceles (hereditary; OMIA-verified breed predisposition)companion_breed_health_pomeranian_omia99_dogPomeranian — Alopecia, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_pomeranian_white_doberman_pinscher_dogPomeranian — White Doberman Pinscher (hereditary; OMIA-verified breed predisposition)companion_breed_health_pony_horse_omia6851_horsePony (Horse) — Familial adenomatous polyposis (hereditary; OMIA-verified breed predisposition)companion_breed_health_pony_of_the_americas_germany_horse_omia4086_horsePony Of the Americas, Germany (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_classical_haemophilia_hemophilia_dogPoodle — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogPoodle, Miniature — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_dalmatian_leukodystrophy_miniature_poodle_demyelination_dogPoodle, Miniature — Dalmatian leukodystrophy; miniature poodle demyelination (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogPoodle, Miniature — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogPoodle, Miniature — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_fibrinoid_leukodystrophy_fibrinoid_encephalomyelopathy_dogPoodle, Miniature — Fibrinoid leukodystrophy, fibrinoid encephalomyelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_globoid_cell_leukodystrophy_dogPoodle, Miniature — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_ichthyosis_syndromic_dogPoodle, Miniature — Ichthyosis, syndromic (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogPoodle, Miniature — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_mps_vi_dogPoodle, Miniature — MPS VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogPoodle, Miniature — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_omia1293_dogPoodle, Miniature — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_omia1311_dogPoodle, Miniature — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_omia1366_dogPoodle, Miniature — Optic nerve hypoplasia, bilateral (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_omia1515_dogPoodle, Miniature — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_omia2489_dogPoodle, Miniature — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_omia2648_dogPoodle, Miniature — Hypocatalasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_osteochondrodysplasia_pseudoachondroplastic_dysplasia_dogPoodle, Miniature — Osteochondrodysplasia; pseudoachondroplastic dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_miniature_progressive_retinal_atrophy_dogPoodle, Miniature — progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_omia2489_dogPoodle — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_omia3521_dogPoodle — Multiple autoimmune diseases syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_omia4994_dogPoodle — Coat colour, dark red (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogPoodle, Standard — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_day_blindness_retinal_degeneration_dogPoodle, Standard — day blindness / retinal degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_dew_claws_canine_preaxial_polydactyly_dogPoodle, Standard — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_hyperuricosuria_and_hyperuricemia_dogPoodle, Standard — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_omia1293_dogPoodle, Standard — Myoclonus epilepsy of Lafora (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_omia1311_dogPoodle, Standard — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_omia2900_dogPoodle, Standard — Neonatal encephalopathy with seizures, ATF2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_omia3473_dogPoodle, Standard — Squamous cell carcinoma of the digit (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_omia3512_dogPoodle, Standard — Amelogenesis imperfecta, ENAM-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_standard_progressive_retinal_atrophy_dogPoodle, Standard — progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_toy_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogPoodle, Toy — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_toy_fibrinoid_leukodystrophy_fibrinoid_encephalomyelopathy_dogPoodle, Toy — Fibrinoid leukodystrophy, fibrinoid encephalomyelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_toy_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogPoodle, Toy — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_toy_mps_vi_dogPoodle, Toy — MPS VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_toy_omia2489_dogPoodle, Toy — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_poodle_toy_omia3364_dogPoodle, Toy — Gangliosidosis, GM2, type II (Sandhoff or variant 0) (hereditary; OMIA-verified breed predisposition)companion_breed_health_portuguese_podengo_omia2489_dogPortuguese Podengo — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_portuguese_podengo_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogPortuguese Podengo — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_portuguese_water_dog_canine_congenital_microphthalmos_with_hematopoietic_defects_dogPortuguese Water Dog — Canine congenital microphthalmos with hematopoietic defects (hereditary; OMIA-verified breed predisposition)companion_breed_health_portuguese_water_dog_dilated_cardiomyopathy_dogPortuguese Water Dog — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_portuguese_water_dog_generalized_pra_gpra_early_onset_progressive_retinal_atrophy_dogPortuguese Water Dog — Generalized PRA (gPRA), early‑onset progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_portuguese_water_dog_omia2489_dogPortuguese Water Dog — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_portuguese_water_dog_omia3009_dogPortuguese Water Dog — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_portuguese_water_dog_omia702_dogPortuguese Water Dog — Gangliosidosis, GM1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_pug_canine_atopic_dermatitis_cad_dogPug — Canine atopic dermatitis (CAD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_pug_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogPug — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_pug_omia1515_dogPug — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_pug_omia2927_dogPug — Vitamin D-deficiency rickets, type IA (hereditary; OMIA-verified breed predisposition)companion_breed_health_pug_omia3145_dogPug — May-Hegglin anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_pug_omia604_dogPug — Entropion (hereditary; OMIA-verified breed predisposition)companion_breed_health_pug_robinow_like_syndrome_curly_tail_dogPug — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_pug_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogPug — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_puli_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogPuli — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_puli_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogPuli — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_puli_omia3923_dogPuli — Bardet-Biedl syndrome 4 (hereditary; OMIA-verified breed predisposition)companion_breed_health_purebred_spanish_horse_also_known_as_swan_neck_turkey_neck_and_upside_down_neck_horsePurebred Spanish (Horse) — also known as Swan Neck, Turkey Neck, and Upside-down Neck (hereditary; OMIA-verified breed predisposition)companion_breed_health_purebred_spanish_horse_congenital_liver_fibrosis_horsePurebred Spanish (Horse) — Congenital liver fibrosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_purebred_spanish_horse_palomino_horsePurebred Spanish (Horse) — Palomino (hereditary; OMIA-verified breed predisposition)companion_breed_health_purebred_spanish_horse_splashed_white_horsePurebred Spanish (Horse) — splashed white (hereditary; OMIA-verified breed predisposition)companion_breed_health_purebred_spanish_horse_splashed_white_macchiato_horsePurebred Spanish (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_pyrenean_mountain_dog_omia3379_dogPyrenean Mountain Dog — Cleft lip and palate (hereditary; OMIA-verified breed predisposition)companion_breed_health_pyrenean_shepherd_bob_tail_bob_tail_dogPyrenean Shepherd — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_pyrenean_shepherd_omia4432_dogPyrenean Shepherd — Laryngeal paralysis and polyneuropathy, CNTNAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_pyrenean_shepherd_this_is_the_classic_m_merle_locus_little_1957_dogPyrenean Shepherd — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_chestnut_horseQuarter Horse (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_equine_juvenile_spinocerebellar_ataxia_ejsca_horseQuarter Horse (Horse) — Equine Juvenile Spinocerebellar Ataxia; EJSCA (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_equine_rhabdomyolysis_syndrome_polysaccharide_storage_myopat_horseQuarter Horse (Horse) — Equine rhabdomyolysis syndrome; Polysaccharide storage myopathy; Tying-up (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_glycogen_storage_disease_iv_gsd_iv_glycogen_storage_disease__horseQuarter Horse (Horse) — Glycogen storage disease IV (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_hyperkalemic_periodic_paralysis_hypp_horseQuarter Horse (Horse) — Hyperkalemic Periodic Paralysis (HYPP) (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_incontinentia_pigmenti_horseQuarter Horse (Horse) — Incontinentia pigmenti (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_myosin_heavy_chain_myopathy_horseQuarter Horse (Horse) — myosin heavy chain myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_omia2113_horseQuarter Horse (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_omia2313_horseQuarter Horse (Horse) — Cerebellar abiotrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_omia3000_horseQuarter Horse (Horse) — Thrombasthenia (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_omia3380_horseQuarter Horse (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_omia3691_horseQuarter Horse (Horse) — Fanconi syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_omia3790_horseQuarter Horse (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_omia483_horseQuarter Horse (Horse) — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_omia5331_horseQuarter Horse (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_overo_lethal_white_foal_syndrome_frame_overo_spotting_horseQuarter Horse (Horse) — Overo lethal white foal syndrome; frame overo spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_palomino_horseQuarter Horse (Horse) — Palomino (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_rhabdomyolysis_with_hyperthermia_anesthesia_induced_malignan_horseQuarter Horse (Horse) — rhabdomyolysis with hyperthermia; anesthesia-induced malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_silver_dapple_horseQuarter Horse (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_splashed_white_horseQuarter Horse (Horse) — splashed white (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_splashed_white_macchiato_horseQuarter Horse (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_quarter_horse_horse_tobiano_sabino_horseQuarter Horse (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_racking_horse_horse_omia5331_horseRacking Horse (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragamuffin_feline_familial_hcm_881_catRagamuffin — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragamuffin_feline_familial_hcm_catRagamuffin — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragdoll_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catRagdoll — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragdoll_dominant_blue_eyes_dbe_catRagdoll — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragdoll_feline_familial_hcm_6367_catRagdoll — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragdoll_feline_familial_hcm_catRagdoll — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragdoll_late_onset_photoreceptor_degeneration_catRagdoll — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragdoll_omia3786_catRagdoll — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_ragdoll_omia652_catRagdoll — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_rat_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogRat Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_rat_terrier_congenital_hypothyroidism_with_goiter_dogRat Terrier — Congenital hypothyroidism with goiter (hereditary; OMIA-verified breed predisposition)companion_breed_health_rat_terrier_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogRat Terrier — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_rat_terrier_omia1271_dogRat Terrier — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_rat_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogRat Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_rat_terrier_recessive_hairlessness_congenital_alopecia_dogRat Terrier — Recessive hairlessness, congenital alopecia (hereditary; OMIA-verified breed predisposition)companion_breed_health_rat_terrier_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogRat Terrier — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_redbone_coonhound_omia1422_dogRedbone Coonhound — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_redbone_coonhound_omia647_dogRedbone Coonhound — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_rex_rabbit_omia2943_rabbitRex (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_rheinische_schecken_rabbit_omia2902_rabbitRheinische Schecken (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_rheinische_schecken_rabbit_omia2943_rabbitRheinische Schecken (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogRhodesian Ridgeback — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_classical_haemophilia_hemophilia_dogRhodesian Ridgeback — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogRhodesian Ridgeback — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_dilute_coat_color_with_neurological_defects_dogRhodesian Ridgeback — Dilute coat color with neurological defects (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_early_onset_adult_deafness_dogRhodesian Ridgeback — Early onset adult deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_epidermolytic_hyperkeratosis_epidermolytic_ichthyosis_dogRhodesian Ridgeback — Epidermolytic hyperkeratosis; epidermolytic ichthyosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_omia1785_dogRhodesian Ridgeback — Ventricular arrhythmias and sudden death (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_omia1851_dogRhodesian Ridgeback — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_omia4007_dogRhodesian Ridgeback — Epilepsy, generalized myoclonic, with photosensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_omia54_dogRhodesian Ridgeback — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_rhodesian_ridgeback_ridge_hair_ridge_dermoid_cyst_dogRhodesian Ridgeback — ridge; hair ridge; dermoid cyst (hereditary; OMIA-verified breed predisposition)companion_breed_health_rocky_mountain_horse_horse_omia3380_horseRocky Mountain Horse (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_rocky_mountain_united_states_of_america_horse_equine_multiple_congenital_ocular_anomalies_previously_known_horseRocky Mountain, United States of America (Horse) — Multiple ocular defects (hereditary; OMIA-verified breed predisposition)companion_breed_health_rocky_mountain_united_states_of_america_horse_omia2177_horseRocky Mountain, United States of America (Horse) — Ocular squamous cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_rocky_mountain_united_states_of_america_horse_omia5331_horseRocky Mountain, United States of America (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_rocky_mountain_united_states_of_america_horse_silver_dapple_horseRocky Mountain, United States of America (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_romanian_mioritic_shepherd_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogRomanian Mioritic Shepherd Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogRottweiler — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_dew_claws_canine_preaxial_polydactyly_dogRottweiler — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_globoid_cell_leukodystrophy_dogRottweiler — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_hereditary_footpad_hyperkeratosis_hfh_dogRottweiler — Hereditary footpad hyperkeratosis (HFH) (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_neuronal_vacuolation_and_spinocerebellar_degeneration_polyne_dogRottweiler — Polyneuropathy, RAB3GAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_nonsyndromic_hearing_loss_dogRottweiler — Nonsyndromic hearing loss (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_omia1188_dogRottweiler — Histiocytosis, malignant (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_omia1271_dogRottweiler — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_omia1311_dogRottweiler — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_omia1373_dogRottweiler — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_omia2999_dogRottweiler — Leukocyte adhesion deficiency, type III (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_omia4119_dogRottweiler — Neuroaxonal dystrophy, VPS11-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_omia54_dogRottweiler — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_omia6865_dogRottweiler — Hypothyroidism and dwarfism, TG-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_references_relating_to_chronic_kidney_disease_are_included_i_dogRottweiler — References relating to chronic kidney disease are included in this entry. (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_the_term_inflammatory_bowel_disease_has_been_used_historical_dogRottweiler — Inflammatory bowel disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_rottweiler_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogRottweiler — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_russell_terrier_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogRussell Terrier — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_russian_blue_omia3786_catRussian Blue — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_russian_blue_omia6412_catRussian Blue — REM sleep behaviour disorder, FAM8A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_russian_blue_omia652_catRussian Blue — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_russian_blue_omia902_catRussian Blue — Hypothyroidism, congenital (hereditary; OMIA-verified breed predisposition)companion_breed_health_russian_bolonka_isolated_growth_hormone_deficiency_dogRussian Bolonka — isolated growth hormone deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_russian_rabbit_omia2943_rabbitRussian (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_s_ddeutsches_kaltblut_germany_horse_tobiano_sabino_horseSüddeutsches Kaltblut, Germany (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_saarloos_wolfhond_dwarfism_pituitary_lhx3_related_pituitary_dwarfism_dogSaarloos Wolfhond — Dwarfism, pituitary, LHX3-related; pituitary dwarfism (hereditary; OMIA-verified breed predisposition)companion_breed_health_saarloos_wolfhond_omia569_dogSaarloos Wolfhond — Pituitary hormone deficiency, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_saarloos_wolfhond_progressive_retinal_central_and_peripheral_neurodegeneration_dogSaarloos Wolfhond — Progressive retinal, central, and peripheral neurodegeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogSaint Bernard — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_dew_claws_canine_preaxial_polydactyly_dogSaint Bernard — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_omia1191_dogSaint Bernard — Malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_omia1311_dogSaint Bernard — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_omia1373_dogSaint Bernard — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_omia2927_dogSaint Bernard — Vitamin D-deficiency rickets, type IA (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_omia4432_dogSaint Bernard — Laryngeal paralysis and polyneuropathy, CNTNAP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_omia54_dogSaint Bernard — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_saint_bernard_polyneuropathy_dogSaint Bernard — polyneuropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_saluki_omia2977_dogSaluki — Neuronal ceroid lipofuscinosis, 8 (hereditary; OMIA-verified breed predisposition)companion_breed_health_saluki_omia4308_dogSaluki — Succinic semialdehyde dehydrogenase deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_saluki_omia6871_dogSaluki — Phloiokeratosis, SUV39H1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_samoyed_alport_syndrome_x_linked_hereditary_nephropathy_glomerulonep_dogSamoyed — Alport syndrome, X-linked hereditary nephropathy, glomerulonephritis, X- linked nephritis (hereditary; OMIA-verified breed predisposition)companion_breed_health_samoyed_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogSamoyed — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_samoyed_omia1271_dogSamoyed — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_samoyed_omia1422_dogSamoyed — Pelger-Huet anomaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_samoyed_omia1500_dogSamoyed — Retinal atrophy, progressive, X-linked, type 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_samoyed_omia2243_dogSamoyed — Syringomyelia (hereditary; OMIA-verified breed predisposition)companion_breed_health_samoyed_omia2997_dogSamoyed — Oculoskeletal dysplasia 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_samoyed_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogSamoyed — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_sapsari_dew_claws_canine_preaxial_polydactyly_dogSapsari — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_sauteur_d_alfort_disrupted_saltatorial_locomotion_sauteur_phenotype_acrobat_rabbitSauteur d'Alfort — disrupted saltatorial locomotion, sauteur phenotype, acrobat (hereditary; OMIA-verified breed predisposition)companion_breed_health_savannah_inherited_retinal_dystrophic_or_degenerative_disorders_early_catSavannah — Retinal atrophy, progressive, KIF3B-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_savannah_late_onset_photoreceptor_degeneration_catSavannah — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_savannah_omia2795_catSavannah — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_savannah_omia652_catSavannah — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_savannah_omia681_catSavannah — Fibrodysplasia ossificans (hereditary; OMIA-verified breed predisposition)companion_breed_health_saxon_gold_omia2902_rabbitSaxon Gold — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_scandinavian_coldblood_trotter_horse_omia3380_horseScandinavian Coldblood Trotter (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_schapendoes_generalized_pra_gpra_early_onset_progressive_retinal_atrophy_dogSchapendoes — Generalized PRA (gPRA), early‑onset progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_schapendoes_omia3097_dogSchapendoes — Neuronal ceroid lipofuscinosis, 6 (hereditary; OMIA-verified breed predisposition)companion_breed_health_schipperke_bob_tail_bob_tail_dogSchipperke — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_schipperke_omia2489_dogSchipperke — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_schipperke_omia2785_dogSchipperke — Mucopolysaccharidosis IIIB (hereditary; OMIA-verified breed predisposition)companion_breed_health_schnauzer_beagle_cross_fetal_onset_neuroaxonal_dystrophy_dogSchnauzer-Beagle Cross — Fetal-onset neuroaxonal dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_schnauzer_congenital_idiopathic_megaesophagus_dogSchnauzer — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_schnauzer_schnauzer_comedo_syndrome_dogSchnauzer — Schnauzer comedo syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_schnauzer_standard_dew_claws_canine_preaxial_polydactyly_dogSchnauzer, Standard — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_schnauzer_standard_omia4240_dogSchnauzer, Standard — Leukodystrophy, TSEN54-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_schnauzer_standard_omia4561_dogSchnauzer, Standard — Cardiomyopathy, dilated, RBM20-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_schnauzer_standard_omia6303_dogSchnauzer, Standard — Stomatocytosis (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_deerhound_also_known_as_pseudoachondroplastic_dysplasia_dogScottish Deerhound — Also known as pseudoachondroplastic dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_deerhound_congenital_hypothyroidism_with_goiter_dogScottish Deerhound — Congenital hypothyroidism with goiter (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_deerhound_cystine_urolithiasis_dogScottish Deerhound — Cystine urolithiasis (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_deerhound_omia647_dogScottish Deerhound — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_deerhound_recessive_hairlessness_congenital_alopecia_dogScottish Deerhound — Recessive hairlessness, congenital alopecia (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catScottish Fold — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_feline_familial_hcm_881_catScottish Fold — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_feline_familial_hcm_catScottish Fold — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_late_onset_photoreceptor_degeneration_catScottish Fold — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_longhair_scottish_fold_scottish_fold_osteochondrodysplasia_sfocd_oste_catScottish Fold Longhair — Scottish fold, Scottish Fold osteochondrodysplasia (SFOCD), osteodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_omia3818_catScottish Fold — Brachycephaly (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_omia4466_catScottish Fold — Cardiomyopathy, hypertrophic, ALMS1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_omia652_catScottish Fold — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_scottish_fold_catScottish Fold — Scottish Fold. (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_fold_scottish_fold_scottish_fold_osteochondrodysplasia_sfocd_oste_catScottish Fold — Scottish fold, Scottish Fold osteochondrodysplasia (SFOCD), osteodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_straight_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catScottish Straight — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_straight_longhair_omia652_catScottish Straight Longhair — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_straight_omia652_catScottish Straight — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_terrier_classical_ehlers_danlos_syndrome_ceds_col5a1_related_ehlers__dogScottish Terrier — classical Ehlers-Danlos syndrome (cEDS), COL5A1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_terrier_dalmatian_leukodystrophy_miniature_poodle_demyelination_dogScottish Terrier — Dalmatian leukodystrophy; miniature poodle demyelination (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_terrier_fibrinoid_leukodystrophy_fibrinoid_encephalomyelopathy_dogScottish Terrier — Fibrinoid leukodystrophy, fibrinoid encephalomyelopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_terrier_hyperuricosuria_and_hyperuricemia_dogScottish Terrier — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_terrier_invasive_transitional_cell_carcinoma_of_the_bladder_canine_i_dogScottish Terrier — Transitional cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_terrier_omia3879_dogScottish Terrier — Ligneous membranitis (hereditary; OMIA-verified breed predisposition)companion_breed_health_scottish_terrier_omia54_dogScottish Terrier — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_sealyham_terrier_omia54_dogSealyham Terrier — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_sealyham_terrier_omia647_dogSealyham Terrier — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_sealyham_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogSealyham Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_selkirk_rex_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catSelkirk Rex — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_selkirk_rex_omia652_catSelkirk Rex — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_selkirk_rex_selkirk_autosomal_dominant_rex_catSelkirk Rex — Selkirk autosomal dominant Rex (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_chestnut_horseShetland Pony (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_omia3715_horseShetland Pony (Horse) — Dwarfism, ACAN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_omia3790_horseShetland Pony (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_omia3870_horseShetland Pony (Horse) — Skeletal atavism (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_omia4086_horseShetland Pony (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_omia4201_horseShetland Pony (Horse) — Coat colour, phaeomelanin dilution, MFSD12-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_silver_dapple_horseShetland Pony (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_splashed_white_macchiato_horseShetland Pony (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_pony_horse_tobiano_sabino_horseShetland Pony (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogShetland Sheepdog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_canine_spongiform_leukoencephalomyelopathy_leucodystrophy_sh_dogShetland Sheepdog — Leukodystrophy, CYTB-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogShetland Sheepdog — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogShetland Sheepdog — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_dew_claws_canine_preaxial_polydactyly_dogShetland Sheepdog — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogShetland Sheepdog — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_invasive_transitional_cell_carcinoma_of_the_bladder_canine_i_dogShetland Sheepdog — Transitional cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_ivermectin_sensitivity_dogShetland Sheepdog — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_omia2998_dogShetland Sheepdog — Gallbladder mucoceles (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_omia4412_dogShetland Sheepdog — Maxillary canine-tooth mesioversion (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_omia4816_dogShetland Sheepdog — Bardet-Biedl syndrome 2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_paroxysmal_exercise_induced_dyskinesia_dogShetland Sheepdog — paroxysmal exercise-induced dyskinesia (hereditary; OMIA-verified breed predisposition)companion_breed_health_shetland_sheepdog_this_is_the_classic_m_merle_locus_little_1957_dogShetland Sheepdog — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_shiba_inu_omia3364_dogShiba Inu — Gangliosidosis, GM2, type II (Sandhoff or variant 0) (hereditary; OMIA-verified breed predisposition)companion_breed_health_shiba_inu_omia3925_dogShiba Inu — Glaucoma, primary open angle (hereditary; OMIA-verified breed predisposition)companion_breed_health_shiba_inu_omia702_dogShiba Inu — Gangliosidosis, GM1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_shiba_inu_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogShiba Inu — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_also_described_as_epidermal_acantholysis_dogShih Tzu — Also described as epidermal acantholysis (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogShih Tzu — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_dew_claws_canine_preaxial_polydactyly_dogShih Tzu — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_intervertebral_disc_disease_hansen_type_i_acute_intervertebr_dogShih Tzu — Intervertebral disc disease; Hansen type I / acute intervertebral disc extrusion (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia1484_dogShih Tzu — Prekallikrein deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia1851_dogShih Tzu — Renal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia3925_dogShih Tzu — Glaucoma, primary open angle (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia4161_dogShih Tzu — Hypothyroidism, congenital dyshormonogenic, with goiter, SLC5A5-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia4642_dogShih Tzu — Vitreous degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia4947_dogShih Tzu — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia54_dogShih Tzu — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia5594_dogShih Tzu — Lissencephaly, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_omia604_dogShih Tzu — Entropion (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_references_relating_to_chronic_kidney_disease_are_included_i_dogShih Tzu — References relating to chronic kidney disease are included in this entry. (hereditary; OMIA-verified breed predisposition)companion_breed_health_shih_tzu_robinow_like_syndrome_curly_tail_dogShih Tzu — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_shiloh_shepherd_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogShiloh Shepherd — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catSiamese — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_late_onset_photoreceptor_degeneration_catSiamese — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_omia1255_catSiamese — Mucopolysaccharidosis VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_omia2942_catSiamese — Porphyria, acute intermittent (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_omia3493_catSiamese — Niemann-Pick disease, type A (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_omia3786_catSiamese — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_omia3875_catSiamese — Glaucoma 3, primary congenital (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_omia3956_catSiamese — Niemann-Pick disease, type C2 (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_omia4255_catSiamese — Hemimelia, radial (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_omia652_catSiamese — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_siamese_x_osteomalacia_catSiamese X — Osteomalacia (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catSiberian — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_dominant_blue_eyes_dbe_catSiberian — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_feline_familial_hcm_6368_catSiberian — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_feline_familial_hcm_catSiberian — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogSiberian Husky — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_classical_haemophilia_hemophilia_dogSiberian Husky — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogSiberian Husky — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_omia1500_dogSiberian Husky — Retinal atrophy, progressive, X-linked, type 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_omia2115_dogSiberian Husky — Goniodysgenesis (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_omia2181_dogSiberian Husky — Hyperphosphatasaemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_omia475_dogSiberian Husky — Cryptorchidism (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_procoagulant_expression_canine_platelet_procoagulant_deficie_dogSiberian Husky — Scott syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_ridge_hair_ridge_dermoid_cyst_dogSiberian Husky — ridge; hair ridge; dermoid cyst (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_husky_this_is_the_classic_b_brown_locus_described_by_little_1957_dogSiberian Husky — This is the classic B (Brown) locus described by Little (1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_omia652_catSiberian — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_siberian_sunshine_catSiberian — Sunshine (hereditary; OMIA-verified breed predisposition)companion_breed_health_silken_windhound_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogSilken Windhound — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_silken_windhound_ivermectin_sensitivity_dogSilken Windhound — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_silky_terrier_omia2489_dogSilky Terrier — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_silver_rabbit_omia2943_rabbitSilver (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_singapura_late_onset_photoreceptor_degeneration_catSingapura — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_singapura_omia2795_catSingapura — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_singapura_omia2929_catSingapura — Coat colour, ticked (Abyssinian) (hereditary; OMIA-verified breed predisposition)companion_breed_health_skye_terrier_omia4947_dogSkye Terrier — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_sloughi_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogSloughi — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_small_swiss_hound_omia3776_dogSmall Swiss Hound — Neuronal ceroid lipofuscinosis, 7 (hereditary; OMIA-verified breed predisposition)companion_breed_health_smithfield_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogSmithfield — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_smooth_fox_terrier_jack_russel_terrier_type_congenital_myasthenic_syndrome_post_dogSmooth Fox Terrier — Myasthenic syndrome, congenital, CHRNE-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_smooth_fox_terrier_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogSmooth Fox Terrier — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_soft_coated_wheaten_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogSoft Coated Wheaten Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_soft_coated_wheaten_terrier_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogSoft Coated Wheaten Terrier — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_somali_late_onset_photoreceptor_degeneration_catSomali — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_somali_omia2795_catSomali — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_somali_progressive_retinal_dystrophy_atrophy_cone_rod_dystrophy_dys_catSomali — Progressive retinal dystrophy/atrophy; Cone-rod dystrophy/dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_spanish_greyhound_omia3122_dogSpanish Greyhound — Hyperekplexia (Startle disease), SLC6A5-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_spanish_water_dog_bob_tail_bob_tail_dogSpanish Water Dog — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_spanish_water_dog_congenital_hypothyroidism_with_goiter_dogSpanish Water Dog — Congenital hypothyroidism with goiter (hereditary; OMIA-verified breed predisposition)companion_breed_health_spanish_water_dog_hyperuricosuria_and_hyperuricemia_dogSpanish Water Dog — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_spanish_water_dog_omia2489_dogSpanish Water Dog — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_spanish_water_dog_omia3009_dogSpanish Water Dog — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_spanish_water_dog_omia3794_dogSpanish Water Dog — Neuroaxonal dystrophy, TECPR2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_spanish_water_dog_omia4391_dogSpanish Water Dog — Retinal atrophy, progressive, PDE6B-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_sphynx_also_called_autosomal_dominant_polycystic_kidney_disease_adp_catSphynx — also called Autosomal Dominant Polycystic Kidney Disease (ADPKD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_sphynx_dominant_blue_eyes_dbe_catSphynx — Dominant blue eyes (DBE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_sphynx_feline_familial_hcm_catSphynx — Feline familial HCM (hereditary; OMIA-verified breed predisposition)companion_breed_health_sphynx_late_onset_photoreceptor_degeneration_catSphynx — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_sphynx_omia4466_catSphynx — Cardiomyopathy, hypertrophic, ALMS1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_sphynx_omia4570_catSphynx — Dyskinesia, paroxysmal (hereditary; OMIA-verified breed predisposition)companion_breed_health_sphynx_omia652_catSphynx — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_sphynx_sphynx_hairless_atrichia_catSphynx — Sphynx hairless; Atrichia (hereditary; OMIA-verified breed predisposition)companion_breed_health_spiti_pony_india_horse_omia3380_horseSpiti Pony, India (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_spotted_saddle_horse_horse_omia5331_horseSpotted Saddle Horse (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_springer_spaniel_congenital_idiopathic_megaesophagus_dogSpringer Spaniel — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_springer_spaniel_omia1311_dogSpringer Spaniel — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_springer_spaniel_shaking_pup_dogSpringer Spaniel — Shaking pup (hereditary; OMIA-verified breed predisposition)companion_breed_health_staffordshire_bull_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogStaffordshire Bull Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_staffordshire_bull_terrier_l_2_hydroxyglutaric_aciduria_dogStaffordshire Bull Terrier — L-2-hydroxyglutaric aciduria (hereditary; OMIA-verified breed predisposition)companion_breed_health_staffordshire_bull_terrier_omia2053_dogStaffordshire Bull Terrier — Myotonia (hereditary; OMIA-verified breed predisposition)companion_breed_health_staffordshire_bull_terrier_omia3379_dogStaffordshire Bull Terrier — Cleft lip and palate (hereditary; OMIA-verified breed predisposition)companion_breed_health_staffordshire_bull_terrier_omia4759_dogStaffordshire Bull Terrier — Congenital muscular dystrophy, LAMA2-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_staffordshire_bull_terrier_primary_hereditary_cataract_dogStaffordshire Bull Terrier — Primary hereditary cataract (hereditary; OMIA-verified breed predisposition)companion_breed_health_staffordshire_bull_terrier_robinow_like_syndrome_curly_tail_dogStaffordshire Bull Terrier — Robinow-like syndrome; curly tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_standardbred_x_tennessee_walking_horse_cross_horse_palomino_horseStandardbred x Tennessee Walking Horse cross (Horse) — Palomino (hereditary; OMIA-verified breed predisposition)companion_breed_health_sussex_spaniel_omia2765_dogSussex Spaniel — Pyruvate dehydrogenase deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_swedish_lapphund_omia2489_dogSwedish Lapphund — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_swedish_lapphund_omia726_dogSwedish Lapphund — Glycogen storage disease II (hereditary; OMIA-verified breed predisposition)companion_breed_health_swedish_vallhund_bob_tail_bob_tail_dogSwedish Vallhund — bob-tail, bob tail (hereditary; OMIA-verified breed predisposition)companion_breed_health_swedish_vallhund_omia4947_dogSwedish Vallhund — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_swedish_vallhund_retinopathy_dogSwedish Vallhund — Retinopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_swedish_warmblood_horse_omia3790_horseSwedish Warmblood (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_swedish_white_elkhound_omia2489_dogSwedish White Elkhound — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_tamaskan_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogTamaskan Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_tamaskan_dog_collie_eye_anomaly_collie_eye_defect_choroidal_hypoplasia_co_dogTamaskan Dog — Choroidal hypoplasia, NHEJ1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_tennessee_rex_late_onset_photoreceptor_degeneration_catTennessee Rex — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_tennessee_rex_omia652_catTennessee Rex — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_tennessee_walking_horse_horse_omia3380_horseTennessee Walking Horse (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_tennessee_walking_horse_horse_omia483_horseTennessee Walking Horse (Horse) — Curly coat (hereditary; OMIA-verified breed predisposition)companion_breed_health_tennessee_walking_horse_horse_omia5331_horseTennessee Walking Horse (Horse) — Night blindness, congenital stationary, GRM6-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_tenterfield_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogTenterfield Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_tenterfield_terrier_congenital_hypothyroidism_with_goiter_dogTenterfield Terrier — Congenital hypothyroidism with goiter (hereditary; OMIA-verified breed predisposition)companion_breed_health_tenterfield_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogTenterfield Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_tenterfield_terrier_spinocerebellar_ataxia_with_myokymia_seizures_or_both_sams_s_dogTenterfield Terrier — Ataxia, cerebellar, KCNJ10-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_th_ringer_rabbit_omia2902_rabbitThüringer (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_th_ringer_rabbit_omia2943_rabbitThüringer (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_thai_ridgeback_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogThai Ridgeback — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_thai_ridgeback_ridge_hair_ridge_dermoid_cyst_dogThai Ridgeback — ridge; hair ridge; dermoid cyst (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_chestnut_horseThoroughbred (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_kyphoscoliotic_ehlers_danlos_syndrome_keds_plod1_related_fra_horseThoroughbred (Horse) — kyphoscoliotic Ehlers-Danlos syndrome (kEDS), PLOD1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_omia2113_horseThoroughbred (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_omia3000_horseThoroughbred (Horse) — Thrombasthenia (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_omia3380_horseThoroughbred (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_omia4086_horseThoroughbred (Horse) — Coat colour, Leopard Complex Spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_omia4757_horseThoroughbred (Horse) — Hypoparathyroidism, RAPGEF5-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_overo_lethal_white_foal_syndrome_frame_overo_spotting_horseThoroughbred (Horse) — Overo lethal white foal syndrome; frame overo spotting (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_rhabdomyolysis_with_hyperthermia_anesthesia_induced_malignan_horseThoroughbred (Horse) — rhabdomyolysis with hyperthermia; anesthesia-induced malignant hyperthermia (hereditary; OMIA-verified breed predisposition)companion_breed_health_thoroughbred_horse_tobiano_sabino_horseThoroughbred (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_mastiff_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogTibetan Mastiff — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_mastiff_omia1373_dogTibetan Mastiff — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_spaniel_familial_oxalate_nephropathy_dogTibetan Spaniel — familial oxalate nephropathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_spaniel_omia4947_dogTibetan Spaniel — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_spaniel_progressive_retinal_atrophy_3_pra3_tibetan_terrier_progressi_dogTibetan Spaniel — Retinal atrophy, progressive, FAM161A-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogTibetan Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_terrier_dwarfism_pituitary_lhx3_related_pituitary_dwarfism_dogTibetan Terrier — Dwarfism, pituitary, LHX3-related; pituitary dwarfism (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_terrier_omia3062_dogTibetan Terrier — Neuronal ceroid lipofuscinosis, 12 (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogTibetan Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_terrier_progressive_retinal_atrophy_3_pra3_tibetan_terrier_progressi_dogTibetan Terrier — Retinal atrophy, progressive, FAM161A-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_terrier_progressive_retinal_atrophy_dogTibetan Terrier — progressive retinal atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_terrier_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogTibetan Terrier — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_tibetan_terrier_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogTibetan Terrier — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_tonkinese_late_onset_photoreceptor_degeneration_catTonkinese — Late-onset photoreceptor degeneration (hereditary; OMIA-verified breed predisposition)companion_breed_health_tori_hobune_estonia_horse_splashed_white_macchiato_horseTori hobune, Estonia (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_tori_hobune_estonia_horse_tobiano_sabino_horseTori hobune, Estonia (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_tosa_dew_claws_canine_preaxial_polydactyly_dogTosa — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_toy_american_eskimo_dog_omia1515_dogToy American Eskimo Dog — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_toy_fox_terrier_congenital_hypothyroidism_with_goiter_dogToy Fox Terrier — Congenital hypothyroidism with goiter (hereditary; OMIA-verified breed predisposition)companion_breed_health_toy_fox_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogToy Fox Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_toyger_omia2542_catToyger — Hair morphology, glitter (hereditary; OMIA-verified breed predisposition)companion_breed_health_toyger_omia2795_catToyger — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_toyger_omia4562_catToyger — Forebrain commissural malformation, ventriculomegaly and interhemispheric cysts, GDF7-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_traditional_gypsy_cob_united_kingdom_of_great_britain_and_no_omia2113_horseTraditional Gypsy Cob, United Kingdom of Great Britain and Northern Ireland (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_traditional_gypsy_cob_united_kingdom_of_great_britain_and_no_palomino_horseTraditional Gypsy Cob, United Kingdom of Great Britain and Northern Ireland (Horse) — Palomino (hereditary; OMIA-verified breed predisposition)companion_breed_health_traditional_gypsy_cob_united_kingdom_of_great_britain_and_no_tobiano_sabino_horseTraditional Gypsy Cob, United Kingdom of Great Britain and Northern Ireland (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_trakehner_horse_omia2313_horseTrakehner (Horse) — Cerebellar abiotrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_trakehner_horse_splashed_white_macchiato_horseTrakehner (Horse) — Splashed white, macchiato (hereditary; OMIA-verified breed predisposition)companion_breed_health_treeing_walker_coonhound_omia2648_dogTreeing Walker Coonhound — Hypocatalasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_treeing_walker_coonhound_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogTreeing Walker Coonhound — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_trottatore_italiano_italy_horse_tobiano_sabino_horseTrottatore Italiano, Italy (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_turkish_angora_omia3786_catTurkish Angora — Multidrug resistance 1, ABCB1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_turkish_angora_omia652_catTurkish Angora — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_turkish_van_omia4734_catTurkish Van — Acrodermatitis enteropathica (hereditary; OMIA-verified breed predisposition)companion_breed_health_turkish_van_omia652_catTurkish Van — Factor XII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_vizsla_omia1373_dogVizsla — Osteochondritis dissecans (hereditary; OMIA-verified breed predisposition)companion_breed_health_vizsla_omia3146_dogVizsla — Exfoliative cutaneous lupus erythematosus (hereditary; OMIA-verified breed predisposition)companion_breed_health_vizsla_omia3634_dogVizsla — Polymyositis (hereditary; OMIA-verified breed predisposition)companion_breed_health_vizsla_omia3907_dogVizsla — Cerebellar cortical degeneration, SNX14-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_vizsla_skeletal_dysplasia_3_disproportionate_dwarfism_dogVizsla — Skeletal dysplasia 3; disproportionate dwarfism (hereditary; OMIA-verified breed predisposition)companion_breed_health_vizsla_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogVizsla — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_volpino_italiano_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogVolpino Italiano — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_vyatka_horse_omia3790_horseVyatka (Horse) — Coat colour, dun (hereditary; OMIA-verified breed predisposition)companion_breed_health_waller_ivermectin_sensitivity_dogWaller — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_warmblood_horse_chestnut_horseWarmblood (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_warmblood_horse_incontinentia_pigmenti_horseWarmblood (Horse) — Incontinentia pigmenti (hereditary; OMIA-verified breed predisposition)companion_breed_health_warmblood_horse_kyphoscoliotic_ehlers_danlos_syndrome_keds_plod1_related_fra_horseWarmblood (Horse) — kyphoscoliotic Ehlers-Danlos syndrome (kEDS), PLOD1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_warmblood_horse_omia2113_horseWarmblood (Horse) — Neuroaxonal dystrophy, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_warmblood_horse_omia838_horseWarmblood (Horse) — Hydrocephalus (hereditary; OMIA-verified breed predisposition)companion_breed_health_warmblood_horse_tobiano_sabino_horseWarmblood (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogWeimaraner — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_classical_haemophilia_hemophilia_dogWeimaraner — classical haemophilia/hemophilia (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_congenital_mirror_movement_disorder_1_dogWeimaraner — Congenital mirror movement disorder 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_dilated_cardiomyopathy_dogWeimaraner — Dilated cardiomyopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_hyperuricosuria_and_hyperuricemia_dogWeimaraner — Hyperuricosuria and hyperuricemia (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_omia1271_dogWeimaraner — Muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_omia1500_dogWeimaraner — Retinal atrophy, progressive, X-linked, type 1 (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_omia2986_dogWeimaraner — Hypomyelination of the central nervous system (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_omia4296_dogWeimaraner — Calvarial hyperostotic syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_omia5063_dogWeimaraner — Lysosomal storage disease, CNP-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_omia5259_dogWeimaraner — Dystonia-ataxia syndrome, paroxysmal, TNR-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_omia54_dogWeimaraner — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_omia6871_dogWeimaraner — Phloiokeratosis, SUV39H1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_references_relating_to_chronic_kidney_disease_are_included_i_dogWeimaraner — References relating to chronic kidney disease are included in this entry. (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_the_term_inflammatory_bowel_disease_has_been_used_historical_dogWeimaraner — Inflammatory bowel disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_x_linked_muscular_dystrophy_dystrophin_deficient_muscular_dy_dogWeimaraner — X-linked muscular dystrophy; Dystrophin-deficient muscular dystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_weimaraner_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogWeimaraner — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_weisse_wiener_rabbit_omia2943_rabbitWeisse Wiener (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_corgi_mps_vi_dogWelsh Corgi — MPS VI (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_corgi_nadh_cytochrome_b5_reductase_deficiency_hereditary_canine_me_dogWelsh Corgi — NADH cytochrome B5 reductase deficiency, hereditary canine methaemoglobinaemia. (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_pony_horse_chestnut_horseWelsh Pony (Horse) — Chestnut (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_pony_horse_myosin_heavy_chain_myopathy_horseWelsh Pony (Horse) — myosin heavy chain myopathy (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_pony_horse_omia2177_horseWelsh Pony (Horse) — Ocular squamous cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_pony_horse_omia2313_horseWelsh Pony (Horse) — Cerebellar abiotrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_pony_horse_palomino_horseWelsh Pony (Horse) — Palomino (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_pony_horse_silver_dapple_horseWelsh Pony (Horse) — Silver dapple (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_pony_horse_tobiano_sabino_horseWelsh Pony (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_sheepdog_this_is_the_classic_m_merle_locus_little_1957_dogWelsh Sheepdog — This is the classic M (Merle) locus (Little, 1957) (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_springer_spaniel_hyperfibrinolysis_dogWelsh Springer Spaniel — Hyperfibrinolysis (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_springer_spaniel_omia4198_dogWelsh Springer Spaniel — Cardiomyopathy, dilated, PLN-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_springer_spaniel_omia647_dogWelsh Springer Spaniel — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogWelsh Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_welsh_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogWelsh Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_west_highland_white_terrier_autosomal_dominant_polycystic_kidney_disease_adpkd_bull_terr_dogWest Highland White Terrier — Polycystic kidney disease (hereditary; OMIA-verified breed predisposition)companion_breed_health_west_highland_white_terrier_canine_atopic_dermatitis_cad_dogWest Highland White Terrier — Canine atopic dermatitis (CAD) (hereditary; OMIA-verified breed predisposition)companion_breed_health_west_highland_white_terrier_globoid_cell_leukodystrophy_dogWest Highland White Terrier — globoid cell leukodystrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_west_highland_white_terrier_invasive_transitional_cell_carcinoma_of_the_bladder_canine_i_dogWest Highland White Terrier — Transitional cell carcinoma (hereditary; OMIA-verified breed predisposition)companion_breed_health_west_highland_white_terrier_l_2_hydroxyglutaric_aciduria_dogWest Highland White Terrier — L-2-hydroxyglutaric aciduria (hereditary; OMIA-verified breed predisposition)companion_breed_health_west_highland_white_terrier_omia1515_dogWest Highland White Terrier — Pyruvate kinase deficiency of erythrocyte (hereditary; OMIA-verified breed predisposition)companion_breed_health_west_highland_white_terrier_omia3876_dogWest Highland White Terrier — Stiff skin syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_west_highland_white_terrier_omia4947_dogWest Highland White Terrier — Chondrodysplasia, FGF4 retrogene-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_wheaten_terrier_xx_sex_reversal_xx_dsd_testicular_ovotesticular_dogWheaten Terrier — XX sex reversal, XX DSD testicular/ovotesticular (hereditary; OMIA-verified breed predisposition)companion_breed_health_whippet_congenital_sensorineural_deafness_dogWhippet — Congenital sensorineural deafness (hereditary; OMIA-verified breed predisposition)companion_breed_health_whippet_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogWhippet — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_whippet_hypermuscularity_gross_muscle_hypertrophy_bully_whippets_dogWhippet — Hypermuscularity; gross muscle hypertrophy; 'bully' whippets (hereditary; OMIA-verified breed predisposition)companion_breed_health_whippet_omia3990_dogWhippet — Retinal atrophy, progressive, Whippet (hereditary; OMIA-verified breed predisposition)companion_breed_health_whippet_omia4152_dogWhippet — Bald thigh syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_whippet_omia647_dogWhippet — Factor VII deficiency (hereditary; OMIA-verified breed predisposition)companion_breed_health_whippet_omia655_dogWhippet — Fanconi syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_whippet_omia729_dogWhippet — Glycogen storage disease VII (hereditary; OMIA-verified breed predisposition)companion_breed_health_white_giant_rabbit_omia2902_rabbitWhite Giant (Rabbit) — Coat colour, extension (hereditary; OMIA-verified breed predisposition)companion_breed_health_white_hotot_rabbit_omia2943_rabbitWhite Hotot (Rabbit) — Coat colour, agouti (hereditary; OMIA-verified breed predisposition)companion_breed_health_white_swiss_shepherd_dog_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogWhite Swiss Shepherd Dog — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_white_swiss_shepherd_dog_cerebellar_hypoplasia_dogWhite Swiss Shepherd Dog — Cerebellar hypoplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_white_swiss_shepherd_dog_congenital_idiopathic_megaesophagus_dogWhite Swiss Shepherd Dog — Congenital idiopathic megaesophagus (hereditary; OMIA-verified breed predisposition)companion_breed_health_white_swiss_shepherd_dog_dwarfism_pituitary_lhx3_related_pituitary_dwarfism_dogWhite Swiss Shepherd Dog — Dwarfism, pituitary, LHX3-related; pituitary dwarfism (hereditary; OMIA-verified breed predisposition)companion_breed_health_white_swiss_shepherd_dog_ivermectin_sensitivity_dogWhite Swiss Shepherd Dog — Ivermectin sensitivity (hereditary; OMIA-verified breed predisposition)companion_breed_health_wire_fox_terrier_canine_degenerative_myelopathy_hereditary_canine_spinal_musc_dogWire Fox Terrier — Canine degenerative myelopathy, hereditary canine spinal muscular atrophy (hereditary; OMIA-verified breed predisposition)companion_breed_health_wire_fox_terrier_omia3873_dogWire Fox Terrier — Van den Ende-Gupta syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_wire_fox_terrier_omia54_dogWire Fox Terrier — Haemophilia B (hereditary; OMIA-verified breed predisposition)companion_breed_health_wire_fox_terrier_omia5594_dogWire Fox Terrier — Lissencephaly, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_wire_fox_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogWire Fox Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_wirehaired_pointing_griffon_juvenile_cataract_fyco1_frameshift_deletion_dogWirehaired Pointing Griffon — Juvenile cataract (FYCO1-frameshift deletion) (hereditary; OMIA-verified breed predisposition)companion_breed_health_wirehaired_pointing_griffon_omia1311_dogWirehaired Pointing Griffon — Narcolepsy (hereditary; OMIA-verified breed predisposition)companion_breed_health_wirehaired_pointing_griffon_omia4461_dogWirehaired Pointing Griffon — Coat colour, roan (hereditary; OMIA-verified breed predisposition)companion_breed_health_working_kelpie_cerebellar_ataxia_dogWorking Kelpie — cerebellar ataxia (hereditary; OMIA-verified breed predisposition)companion_breed_health_working_kelpie_omia5077_dogWorking Kelpie — Cerebellar abiotrophy, VMP1-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_xoloitzcuintli_canine_ectodermal_dysplasia_dogXoloitzcuintli — Canine ectodermal dysplasia (hereditary; OMIA-verified breed predisposition)companion_breed_health_xoloitzcuintli_schnauzer_comedo_syndrome_dogXoloitzcuintli — Schnauzer comedo syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_alaskan_husky_encephalopathy_ahe_dogYorkshire Terrier — Alaskan Husky Encephalopathy (AHE) (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_colour_mutant_alopecia_color_dilution_alopecia_colour_diluti_dogYorkshire Terrier — Coat colour, dilution, MLPH-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_dew_claws_canine_preaxial_polydactyly_dogYorkshire Terrier — Dew claws, canine preaxial polydactyly (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_disease_is_also_called_type_1_von_willebrand_disease_vwdi_an_dogYorkshire Terrier — Von Willebrand disease I (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_ectodermal_dysplasia_x_linked_x_linked_hypohidrotic_ectoderm_dogYorkshire Terrier — Hypohidrotic ectodermal dysplasia, X-linked, EDA-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_l_2_hydroxyglutaric_aciduria_dogYorkshire Terrier — L-2-hydroxyglutaric aciduria (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_omia2489_dogYorkshire Terrier — Progressive rod-cone degeneration, PRCD-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_omia3662_dogYorkshire Terrier — XY difference of sexual development, generic (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_omia3879_dogYorkshire Terrier — Ligneous membranitis (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_omia655_dogYorkshire Terrier — Fanconi syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_persistent_m_llerian_duct_syndrome_dogYorkshire Terrier — Persistent Müllerian Duct Syndrome (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_primary_lens_luxation_isolated_canine_ectopia_lentis_luxatio_dogYorkshire Terrier — Primary lens luxation; isolated canine ectopia lentis; luxatio lentis (hereditary; OMIA-verified breed predisposition)companion_breed_health_yorkshire_terrier_ridge_hair_ridge_dermoid_cyst_dogYorkshire Terrier — ridge; hair ridge; dermoid cyst (hereditary; OMIA-verified breed predisposition)companion_breed_health_zangersheide_belgium_horse_tobiano_sabino_horseZangersheide, Belgium (Horse) — Tobiano, Sabino (hereditary; OMIA-verified breed predisposition)companion_breed_health_zaniskari_pony_horse_omia3380_horseZaniskari Pony (Horse) — Gaitedness, DMRT3-related (hereditary; OMIA-verified breed predisposition)companion_breed_health_zika_hungary_rabbit_omia423_rabbitZika, Hungary (Rabbit) — Coat/skin colour, oculocutaneous albinism type I (OCA1), TYR-related (hereditary; OMIA-verified breed predisposition)