OMIA:001568-9986 : Narrow axis in Oryctolagus cuniculus (rabbit)

Categories: Skeleton phene (incl. short stature & teeth)

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal recessive

Considered a defect: yes

Key variant known: no

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2011). OMIA:001568-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset].


1983 Crary, DD., Fox, RR. :
Narrow axis: an inherited anomaly of the second cervical vertebra in the rabbit. J Hered 74:47-50, 1983. Pubmed reference: 6827069.

Edit History

  • Created by Frank Nicholas on 27 May 2011