ATP7B, ATPase copper transporting beta, 540

N. diseases: 182; N. variants: 333
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
0.440 GeneticVariation disease BEFREE SHED and SHED-Heps were transplanted into WD model Atp7b-mutated Long-Evans Cinnamon (LEC) rats received copper overloading to induce a lethal fulminant liver failure. 30733544 2019
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
0.440 Biomarker disease CTD_human Wilson disease (WD) is caused by accumulation of excess copper (Cu) due to a mutation in the gene encoding the liver Cu transporter ATP7B, and is characterized by acute liver failure or cirrhosis and neuronal cell death. 25134866 2014
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
0.440 Biomarker disease BEFREE Wilson disease (WD) is caused by accumulation of excess copper (Cu) due to a mutation in the gene encoding the liver Cu transporter ATP7B, and is characterized by acute liver failure or cirrhosis and neuronal cell death. 25134866 2014
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
0.440 GeneticVariation disease BEFREE High prevalence of fulminant hepatic failure among patients with mutant alleles for truncation of ATP7B in Wilson's disease. 20491539 2010
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
0.440 GeneticVariation disease BEFREE We examined the ATP7B gene in two Japanese sisters with Wilson's disease presenting with fulminant hepatic failure but who did not exhibit Kayser-Fleischer rings or abnormal neurological findings. 10777157 2000
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute
0.440 Biomarker disease HPO