OMIA:000249-9986 : Cyclopia in Oryctolagus cuniculus (rabbit) |
In other species: chicken , dog , domestic cat , horse , pig , taurine cattle , sheep , American mink
Categories: Vision / eye phene , Craniofacial phene
Mendelian trait/disorder: yes
Mode of inheritance: Autosomal recessive
Disease-related: 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
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2016). OMIA:000249-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
1958 | Robinson, R. : |
Genetic studies of the rabbit. Bibliographia Genetica 17:229–558, 1958. |
Edit History
- Created by Frank Nicholas on 29 Apr 2016