ATP7B, ATPase copper transporting beta, 540

N. diseases: 182; N. variants: 333
Disease: Indian childhood cirrhosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268074
Disease: Indian childhood cirrhosis
Indian childhood cirrhosis 		0.010 Biomarker disease BEFREE The ATP7B gene has been excluded in the much rarer human copper overload disease non-Indian childhood cirrhosis, indicating genetic heterogeneity. 9949209 1999