KRT85, keratin 85, 3891

N. diseases: 14; N. variants: 2
Disease: NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3279947
Disease: NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 		0.010 GeneticVariation disease BEFREE Sequence analysis of the coding regions of keratin KRTHB5 gene, previously associated with a distinct clinical form of hair-nail dysplasia, revealed normal coding regions. 20409997 2010