OMIA 001071 : Wilson disease |
Possible human homologues (MIM numbers):
277900 (trait)
,
606882 (gene)
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).
Species in which this phene is found:
dog (Canis lupus familiaris)
domestic cat (Felis catus)
pig (Sus scrofa)
cattle (Bos taurus)
sheep (Ovis aries)
dog (Canis lupus familiaris)
domestic cat (Felis catus)
pig (Sus scrofa)
cattle (Bos taurus)
sheep (Ovis aries)
Edit History
- Created by Frank Nicholas on 03 May 2005
- Changed by Frank Nicholas on 29 Sep 2011
- Changed by Frank Nicholas on 22 Oct 2012
- Changed by Frank Nicholas on 25 Oct 2016
- Changed by Imke Tammen2 on 14 Aug 2021
- Changed by Imke Tammen2 on 01 Dec 2021