OMIA:001071-9823 : Wilson disease in Sus scrofa (pig)

In other species: dog , domestic cat , taurine cattle , sheep

Categories: Liver/biliary system phene

Links to possible relevant human trait(s) and/or gene(s) in OMIM: 277900 (trait) , 606882 (gene)

Links to relevant human diseases in MONDO:

Single-gene trait/disorder: unknown

Disease-related: yes

Cross-species summary: A disorder of copper metabolism, due to a deficiency of ceruloplasmin, which forms a complex with copper. The excess copper is deposited in the brain (causing mental retardation) or the liver (causing jaundice and cirrhosis).

Cite this entry

Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:001071-9823: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70

Reference

1987 Howell, J.M., Wiener, G., Gawthorne, J.M. :
The genetics of copper metabolism in animals and man :45-61, 1987.

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  • Created by Frank Nicholas on 06 Sep 2005