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)

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