Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 285025
Gene Symbol: CCDC141
CCDC141
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.320 GermlineCausalMutation ORPHANET Our studies revealed nine affected individuals from four independent families in which IHH/KS is associated with inactivating CCDC141 variants, revealing a prevalence of 3.3%. 28324054

2017
Entrez Id: 285025
Gene Symbol: CCDC141
CCDC141
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.320 SusceptibilityMutation ORPHANET Our studies revealed nine affected individuals from four independent families in which IHH/KS is associated with inactivating CCDC141 variants, revealing a prevalence of 3.3%. 28324054

2017