--- license: permission_granted topic_id: companion_species_health_brachydactyly_rabbit category: companion-species-health title: "Rabbit (Oryctolagus cuniculus) — Brachydactyly (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_brachydactyly_3849.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_brachydactyly_rabbit/01_companion_species_health_brachydactyly_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) — Brachydactyly (hereditary; OMIA-verified species predisposition)" url: "https://omia.org/OMIA000146/9986/" 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) — Brachydactyly (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: BrachydactylySummary: See Robinson (1958, pp. 341-342)
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: br (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.
- 1958. Genetic studies of the rabbit. Bibliographia Genetica — OMIA Phene_Article / Article
- 1935. Hereditary brachydactylia and associated abnormalities in the rabbit. Science — PubMed:PMID17799086 | DOI:10.1126/science.81.2104.405-a — OMIA Phene_Article / Article
- 1939. Hereditary brachydactylia and allied abnormalities in the rabbit. J Exp Med — PubMed:PMID19870848 | DOI:10.1084/jem.69.2.301 — OMIA Phene_Article / Article
- 1977. Simultaneous prevention of blood abnormalities and hereditary congenital amputations in a brachydactylous rabbit stock. Teratology — PubMed:PMID301294 | DOI:10.1002/tera.1420150204 — OMIA Phene_Article / Article
- 1984. Prevention of thrombocytic defects in the br/br rabbit with folic acid and vitamin B12: analogy with the T.A.R. syndrome in humans. Int J Vitam Nutr Res — PubMed:PMID6500844 — OMIA Phene_Article / Article
- 1989. Animal models with inherited hematopoietic abnormalities as tools to study thrombopoiesis. Blood Cells — PubMed:PMID2649183 — OMIA Phene_Article / Article