Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51098
Gene Symbol: IFT52
IFT52
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.300 Biomarker GENOMICS_ENGLAND A homozygous nonsense variant in IFT52 is associated with a human skeletal ciliopathy. 26880018

2016