OMIA:000753-9986 : Osteodystrophy in Oryctolagus cuniculus (rabbit)

In other species: dog , domestic cat , taurine cattle

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

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 103580 (trait) , 600430 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

Genetic engineering: Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000753-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset].


1996 Anon. :
Osteodystrophy in rabbits Journal of Small Animal Practice 37:512, 1996.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005