Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55764
Gene Symbol: IFT122
IFT122
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		0.300 Biomarker CTD_human Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene. 20493458

2010