KRT8, keratin 8, 3856

N. diseases: 166; N. variants: 16
Disease: Cirrhosis, Familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.500 GeneticVariation disease UNIPROT Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies. 12724528 2003
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.500 Biomarker disease CTD_human