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Rabbit (Oryctolagus cuniculus) — Epilepsy (hereditary; OMIA-verified species predisposition)

companion_species_health_epilepsy_rabbit

companion-species-health en

--- license: permission_granted topic_id: companion_species_health_epilepsy_rabbit category: companion-species-health title: "Rabbit (Oryctolagus cuniculus) — Epilepsy (hereditary; OMIA-verified species predisposition)" lang: en source: "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." source_file: pdf-raw/species-health/rabbit_epilepsy_2265.txt date_parsed: 2026-08-24 tokens_estimated: 80 verification: method: substring_match claims: 3 passed: 3 date: 2026-08-24 recovered: false path: companion-species-health/companion_species_health_epilepsy_rabbit/01_companion_species_health_epilepsy_rabbit.md source_document: "OMIA — Online Mendelian Inheritance in Animals (University of Sydney)" citation: authority: "OMIA — Online Mendelian Inheritance in Animals (University of Sydney)" title: "Rabbit (Oryctolagus cuniculus) — Epilepsy (hereditary; OMIA-verified species predisposition)" url: "https://omia.org/OMIA000344/9986/" retrieved: "2026-08-24" ref: "OMIA species-specific hereditary-disorder records (omia.org), derived from local OMIA database dump; dataset: https://doi.org/10.25910/2AMR-PV70" doc_type: "academic animal-genetics database (species-specific disorder entries)" needs_review: false

verification_derived: method: derived_from_dataset source: "OMIA database dump (omia.xml, local); fields Gene/Variant/Article/OMIM" 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."---

Rabbit (Oryctolagus cuniculus) — Epilepsy (hereditary; OMIA-verified species predisposition)

Source: 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.

Claims

  • Species: Rabbit (Oryctolagus cuniculus)
  • Disorder: Epilepsy
  • Summary: See Robinson (1958, pp. 331-333).

Associated gene(s)

Derived 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.

  • OMIA entry symbol: ep (no structured Phene_Gene link)

Evidence (references)

Derived 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.

  • 1979. Genetic animal models of epilepsy. Introduction. Fed Proc — PubMed:PMID478016 — OMIA Phene_Article / Article
  • 1957. Familial epileptiform disease in a breed of rabbits. Wiener Tierärztliche Monatsschrift — OMIA Phene_Article / Article
  • 1958. Genetic studies of the rabbit. Bibliographia Genetica — OMIA Phene_Article / Article
  • 1955. Recent genetics of the domestic rabbit. Adv Genet — PubMed:PMID13258375 | DOI:10.1016/s0065-2660(08)60096-6 — OMIA Phene_Article / Article

Comparative medicine (human OMIM)

Derived 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.

  • OMIM:104130 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:117100 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:121200 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:121201 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:125370 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:132090 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:132100 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:132300 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:159600 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:182610 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:203600 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:208700 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:220300 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:226750 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:226800 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:226810 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:226850 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:254770 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:254780 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:254800 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:266270 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:267740 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:270805 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:301900 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:310370 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:545000 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:600131 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:600143 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:600512 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:600513 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:600669 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:601068 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
  • OMIM:245570 (type: trait) — OMIA Group_OMIM (via OMIA_ID)

Sources

Rabbit (Oryctolagus cuniculus) — Epilepsy (hereditary; OMIA-verified species predisposition)
companion-species-healthPMID 478016

Machine access

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