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
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000753-9986: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 1996 | Anon. : |
| Osteodystrophy in rabbits Journal of Small Animal Practice 37:512, 1996. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005