Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 54551
Gene Symbol: MAGEL2
MAGEL2
CUI: C3809877
Disease: Prader-Willi-like syndrome
Prader-Willi-like syndrome 		0.700 CausalMutation CLINVAR Molecular diagnostic experience of whole-exome sequencing in adult patients. 26633545

2016
Entrez Id: 54551
Gene Symbol: MAGEL2
MAGEL2
CUI: C3809877
Disease: Prader-Willi-like syndrome
Prader-Willi-like syndrome 		0.700 CausalMutation CLINVAR Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. 24076603

2013
Entrez Id: 54551
Gene Symbol: MAGEL2
MAGEL2
CUI: C3809877
Disease: Prader-Willi-like syndrome
Prader-Willi-like syndrome 		0.700 GeneticVariation CLINVAR