MAGEL2, MAGE family member L2, 54551

N. diseases: 184; N. variants: 15
Disease: Pituitary Diseases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0032002
Disease: Pituitary Diseases
Pituitary Diseases 		0.010 GeneticVariation group BEFREE This study highlights the association of hypothalamo-pituitary disease with MAGEL2 and L1CAM mutations. 31504653 2019