--- license: permission_granted topic_id: companion_species_health_h_ydrocephalia_rabbit category: companion-species-health title: "Rabbit (Oryctolagus cuniculus) — H ydrocephalia (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_h_ydrocephalia_840.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_h_ydrocephalia_rabbit/01_companion_species_health_h_ydrocephalia_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) — H ydrocephalia (hereditary; OMIA-verified species predisposition)" url: "https://omia.org/OMIA000487/9986/" 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." 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) — H ydrocephalia (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: H ydrocephaliaSummary: See Robinson (1958, pp. 333-334).
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.
- 1966. Hydrocephalus and cleft palate in an inbred rabbit colony. Journal of Heredity — PubMed:PMID6007532 — OMIA Phene_Article / Article
- 1958. Genetic studies of the rabbit. Bibliographia Genetica — 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:109400 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:112240 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:123155 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:209970 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236600 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236635 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236640 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236660 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236670 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236690 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:273730 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:276950 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:307000 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:307010 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:314390 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:123155 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:600257 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:600559 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:600991 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:615181 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
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.
- 1966. Hydrocephalus and cleft palate in an inbred rabbit colony. Journal of Heredity — PubMed:PMID6007532 — OMIA Phene_Article / Article
- 1958. Genetic studies of the rabbit. Bibliographia Genetica — 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:109400 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:112240 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:123155 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:209970 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236600 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236635 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236640 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236660 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236670 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:236690 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:273730 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:276950 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:307000 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:307010 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:314390 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:123155 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:600257 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:600559 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:600991 (type: trait) — OMIA Group_OMIM (via OMIA_ID)
- OMIM:615181 (type: trait) — OMIA Group_OMIM (via OMIA_ID)