Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8239
Gene Symbol: USP9X
USP9X
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.300 Biomarker GENOMICS_ENGLAND De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations. 26833328

2016