Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9915
Gene Symbol: ARNT2
ARNT2
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
0.300 GermlineCausalMutation ORPHANET ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies. 24022475

2013