OMIA:000753-9685 : Osteodystrophy in Felis catus (domestic cat)

In other species: dog , taurine cattle , rabbit

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

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 103580 (trait) , 600430 (trait)

Mendelian trait/disorder: yes

Considered a defect: yes

Key variant known: no

Species-specific name: Scottish Fold osteodystrophy

Breed: Scottish Fold (Cat) (VBO_0100209).
Breeds in which the phene has been documented. (If a likely causal variant has been documented for the phene, see the variant table breeds in which the variant has been reported).

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000753-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset].


1995 Mathews, K.G., Koblik, P.D., Knoeckel, M.J., Pool, R.R., Fyfe, J.C. :
Resolution of lameness associated with Scottish fold osteodystrophy following bilateral ostectomies and pantarsal arthrodeses Journal of the American Animal Hospital Association 31:280-288, 1995. Pubmed reference: 7552658.

Edit History

  • Created by Frank Nicholas on 06 Sep 2005