PRKCSH, protein kinase C substrate 80K-H, 5589

N. diseases: 44; N. variants: 5
Disease: Liver diseases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.040 Biomarker group BEFREE However, the role of hepatocystin in hepatitis B virus-related liver disease remains unknown. 24769044 2014
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.040 GeneticVariation group LHGDN Abnormal hepatocystin caused by truncating PRKCSH mutations leads to autosomal dominant polycystic liver disease. 15057895 2004
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.040 GeneticVariation group LHGDN Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease. 12529853 2003
CUI: C0023895
Disease: Liver diseases
Liver diseases 		0.040 GeneticVariation group LHGDN Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease. 12577059 2003