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Rabbit (Oryctolagus cuniculus) — Ataxia, generic (hereditary; OMIA-verified species predisposition)

companion_species_health_ataxia_generic_rabbit

companion-species-health 708 tok en 2026-08-24

Rabbit (Oryctolagus cuniculus) — Ataxia, generic (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: Ataxia, generic
  • Summary: See Robinson (1958, p. 330-331)

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: ax (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.

  • 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
  • 1962. Hereditary ataxia of rabbits. Histopathological alterations. Arch Neurol — PubMed:PMID14480890 | DOI:10.1001/archneur.1962.00450200037004 — OMIA Phene_Article / Article
  • 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
  • 1965. Ultrastructural lesions in rabbit hereditary ataxia. Arch Neurol — PubMed:PMID5832261 | DOI:10.1001/archneur.1965.00470030018002 — OMIA Phene_Article / Article
  • 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
  • 1966. Carbohydrate metabolites in rabbit hereditary ataxia. Arch Neurol — PubMed:PMID5912009 | DOI:10.1001/archneur.1966.00470150061010 — OMIA Phene_Article / Article
  • 1967. Glycogen and glycolytic intermediates in rabbit hereditary ataxia. J Neuropathol Exp Neurol — PubMed:PMID6022138 — OMIA Phene_Article / Article
  • 1967. Inositide metabolism in rabbit hereditary ataxia. Arch Neurol — PubMed:PMID4293372 | DOI:10.1001/archneur.1967.00470300103017 — OMIA Phene_Article / Article
  • 1968. Hereditary ataxia of animals. Arch Neurol — PubMed:PMID5676918 | DOI:10.1001/archneur.1968.00480010052003 — OMIA Phene_Article / Article
  • 1970. Glucose 14C metabolism in rabbit hereditary ataxia. Arch Neurol — PubMed:PMID5435666 | DOI:10.1001/archneur.1970.00480230063007 — OMIA Phene_Article / Article
  • 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

Sources

Rabbit (Oryctolagus cuniculus) — Ataxia, generic (hereditary; OMIA-verified species predisposition)
Source document: OMIA — Online Mendelian Inheritance in Animals (University of Sydney)
OMIA — Online Mendelian Inheritance in Animals (University of Sydney)OMIA species-specific hereditary-disorder records (omia.org), derived from local OMIA database dump; dataset: https://doi.org/10.25910/2AMR-PV70retrieved 2026-08-24

Verification file: pdf-raw/species-health/rabbit_ataxia_generic_3847.txt