PRKD1, protein kinase D1, 5587

N. diseases: 171; N. variants: 19
Disease: Hepatic Fibrosis, Congenital ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		0.010 Biomarker disease BEFREE Autosomal recessive polycystic kidney disease (ARPKD) is an infantile form of PKD characterized by fusiform dilation of collecting ducts and congenital hepatic fibrosis. 12925574 2003