Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3848
Gene Symbol: KRT1
KRT1
CUI: C1836681
Disease: Erythrokeratoderma, Reticular
Erythrokeratoderma, Reticular 		0.300 GermlineCausalMutation ORPHANET Frequent somatic reversion of KRT1 mutations in ichthyosis with confetti. 25774499

2015