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OMIA:000750-9850 : Osteochondrosis in Cervidae (deer)

In other species: chicken , dog , domestic cat , horse , pig , taurine cattle , indicine cattle (zebu) , sheep , raccoon dog

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

Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 181440 (trait) , 188700 (trait) , 259200 (trait)

Links to MONDO diseases: No links.

Mendelian trait/disorder: unknown

Considered a defect: yes

Cross-species summary: Abnormal growth ossification centers in young, growing animals. Initially a degeneration/ necrosis followed by regeneration or recalcification. Osteochondrosis (OC) lesions that result is bone or cartilage fragments are called osteochondritis dissecans (OCD) - see OMIA000748.

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:000750-9850: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1995 Audige, L., Wilson, P.R., Morris, R.S., Davidson, G.W. :
Osteochondrosis, skeletal abnormalities and enzootic ataxia associated with copper deficiency in a farmed red deer (Cervus elaghus) herd New Zealand Veterinary Journal 43:70-76, 1995.

Edit History


  • Created by Frank Nicholas on 06 Sep 2005