Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 26012
Gene Symbol: NSMF
NSMF
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.340 GermlineCausalMutation ORPHANET Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism. 17235395

2007