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

In other species: dog , taurine cattle , rabbit

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: yes

Considered a defect: yes

Key variant known: no

Species-specific name: Scottish Fold osteodystrophy

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

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

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:000753-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

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