NDN, necdin, MAGE family member, 4692

N. diseases: 124; N. variants: 2
Disease: Kallmann Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		0.010 GeneticVariation disease BEFREE A heterozygous variant of necdin, p.V318A, was identified in a 23-year-old male with Kallmann syndrome. 21543378 2011