OMIA:000249-9986 : Cyclopia in Oryctolagus cuniculus
Categories: Craniofacial phene
Links to MONDO diseases: No links.
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Considered a defect: yes
Key variant known: no
Cross-species summary: A congenital developmental disorder characterised by a single orbital fossa (eye socket). Named after the race of one-eyed giants of Greek mythology. In humans, this disorder is often associated with a chromosomal abnormality.
Species-specific description: See Robinson (1958, p. 348)
Cite this entry
|1958||Robinson, R. :|
|Genetic studies of the rabbit. Bibliographia Genetica 17:229–558, 1958.|
- Created by Frank Nicholas on 29 Apr 2016