Gene: DSG4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 147409
Gene Symbol: DSG4
DSG4 		0.300 GermlineCausalMutation disease ORPHANET Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins. 16770573 2006