Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55717
Gene Symbol: WDR11
WDR11
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.740 GermlineCausalMutation ORPHANET WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. 20887964

2010