Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10371
Gene Symbol: SEMA3A
SEMA3A
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.360 GermlineCausalMutation ORPHANET SEMA3A is therefore a new gene whose loss-of-function is involved in KS. 22416012

2012