{"topic_id":"companion_species_health_ataxia_generic_rabbit","category":"companion-species-health","context":"---\nlicense: permission_granted\ntopic_id: companion_species_health_ataxia_generic_rabbit\ncategory: companion-species-health\ntitle: \"Rabbit (Oryctolagus cuniculus) — Ataxia, generic (hereditary; OMIA-verified species predisposition)\"\nlang: en\nsource: \"OMIA (Online Mendelian Inheritance in Animals, University of Sydney) species-specific hereditary-disorder record, saved verbatim to source_file; C1 substring-verified. Pulled 2026-08-24 from local OMIA database dump.\"\nsource_file: pdf-raw/species-health/rabbit_ataxia_generic_3847.txt\ndate_parsed: 2026-08-24\ntokens_estimated: 80\nverification:\n  method: substring_match\n  claims: 3\n  passed: 3\n  date: 2026-08-24\nrecovered: false\npath: companion-species-health/companion_species_health_ataxia_generic_rabbit/01_companion_species_health_ataxia_generic_rabbit.md\nsource_document: \"OMIA — Online Mendelian Inheritance in Animals (University of Sydney)\"\ncitation:\n  authority: \"OMIA — Online Mendelian Inheritance in Animals (University of Sydney)\"\n  title: \"Rabbit (Oryctolagus cuniculus) — Ataxia, generic (hereditary; OMIA-verified species predisposition)\"\n  url: \"https://omia.org/OMIA000077/9986/\"\n  retrieved: \"2026-08-24\"\n  ref: \"OMIA species-specific hereditary-disorder records (omia.org), derived from local OMIA database dump; dataset: https://doi.org/10.25910/2AMR-PV70\"\n  doc_type: \"academic animal-genetics database (species-specific disorder entries)\"\n  needs_review: false\n\nverification_derived:\n  method: derived_from_dataset\n  source: \"OMIA database dump (omia.xml, local); fields Gene/Variant/Article/OMIM\"\n  note: \"Structured fields (gene, variant rsID/protein change, PubMed/DOI references, OMIM cross-link) extracted from OMIA dump and presented with first-hand values; not verbatim prose.\"---\n\n# Rabbit (Oryctolagus cuniculus) — Ataxia, generic (hereditary; OMIA-verified species predisposition)\n\nSource: first-hand OMIA (University of Sydney) species-specific hereditary-disorder record, saved verbatim to `source_file`; every claim below is a C1 byte-substring of it.\n\n## Claims\n\n- `Species: Rabbit (Oryctolagus cuniculus)`\n- `Disorder: Ataxia, generic`\n- `Summary: See Robinson (1958, p. 330-331)`\n## Associated gene(s)\nDerived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.\n- OMIA entry symbol: ax (no structured Phene_Gene link)\n\n## Evidence (references)\nDerived from OMIA database dump (omia.xml, local); structured field, not verbatim prose. First-hand values below are verbatim substrings of the topic's pdf-raw/omia/<phene_id>.txt source file.\n- 1942. \"Ataxia,\" a Hereditary Nervous Disorder of the Rabbit. Proc Natl Acad Sci U S A — PubMed:PMID16588528 | DOI:10.1073/pnas.28.4.123 — OMIA Phene_Article / Article\n- 1962. Hereditary ataxia of rabbits. Histopathological alterations. Arch Neurol — PubMed:PMID14480890 | DOI:10.1001/archneur.1962.00450200037004 — OMIA Phene_Article / Article\n- 1964. Hereditary ataxia in the rabbit: amino acid analyses of blood and brain. J Nerv Ment Dis — PubMed:PMID14206450 | DOI:10.1097/00005053-196408000-00004 — OMIA Phene_Article / Article\n- 1965. Ultrastructural lesions in rabbit hereditary ataxia. Arch Neurol — PubMed:PMID5832261 | DOI:10.1001/archneur.1965.00470030018002 — OMIA Phene_Article / Article\n- 1966. [Familial ataxia of the rabbit, different from the hereditary disease of Sawin-Anders. Preliminary communication]. Acta Neuropathol — PubMed:PMID6006977 | DOI:10.1007/BF00687854 — OMIA Phene_Article / Article\n- 1966. Carbohydrate metabolites in rabbit hereditary ataxia. Arch Neurol — PubMed:PMID5912009 | DOI:10.1001/archneur.1966.00470150061010 — OMIA Phene_Article / Article\n- 1967. Glycogen and glycolytic intermediates in rabbit hereditary ataxia. J Neuropathol Exp Neurol — PubMed:PMID6022138 — OMIA Phene_Article / Article\n- 1967. Inositide metabolism in rabbit hereditary ataxia. Arch Neurol — PubMed:PMID4293372 | DOI:10.1001/archneur.1967.00470300103017 — OMIA Phene_Article / Article\n- 1968. Hereditary ataxia of animals. Arch Neurol — PubMed:PMID5676918 | DOI:10.1001/archneur.1968.00480010052003 — OMIA Phene_Article / Article\n- 1970. Glucose 14C metabolism in rabbit hereditary ataxia. Arch Neurol — PubMed:PMID5435666 | DOI:10.1001/archneur.1970.00480230063007 — OMIA Phene_Article / Article\n- 1974. Familial ataxia of the rabbit Sawin-Anders type. Ultrastructural analysis of degeneration of the cochlear nuclei. Acta Neuropathol — PubMed:PMID4446957 | DOI:10.1007/BF00685318 — OMIA Phene_Article / Article\n","sources":["companion-species-health — Rabbit (Oryctolagus cuniculus) — Ataxia, generic (hereditary; OMIA-verified species predisposition)"],"source":{"authority":"companion-species-health","title":"Rabbit (Oryctolagus cuniculus) — Ataxia, generic (hereditary; OMIA-verified species predisposition)","url":"https://pubmed.ncbi.nlm.nih.gov/16588528/","retrieved":"","ref":"PMID 16588528","doc_type":"official source","source_document":"","verification_file":""},"source_document":"","source_file":"","trust":{"authority_tier":"ungraded","fidelity":"verbatim","license":null,"display_grade":"pending"},"tokens_estimated":670,"generated_at":null,"tip":"Use /api/v1/topics to discover more topics. /api/v1/nutrient for precise single-point queries. /api/v1/cross_compare for 2-3 standard comparisons."}