Gene: IFT43 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 112752
Gene Symbol: IFT43
IFT43 		0.110 Biomarker disease BEFREE De novo 14q24.2q24.3 microdeletion including IFT43 is associated with intellectual disability, skeletal anomalies, cardiac anomalies, and myopia. 26892345 2016
Entrez Id: 112752
Gene Symbol: IFT43
IFT43 		0.110 Biomarker disease HPO