KRT25, keratin 25, 147183

N. diseases: 25; N. variants: 3
Disease: HYPOTRICHOSIS 8 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.100 CausalMutation disease CLINVAR A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hair. 26160856 2015