OMIA 000249-9986 : Cyclopia in Oryctolagus cuniculus

In other species: chicken , dog , domestic cat , horse , pig , cattle , sheep , American mink

Possibly relevant human trait(s) and/or gene(s) (MIM number): 236100

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)

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