Gene: MFN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9927
Gene Symbol: MFN2
MFN2 		0.110 GeneticVariation disease BEFREE Autosomal-dominant inheritance of a R94Q mutation in MFN2 causes the axonal subtype 2A2A which is characterized by early onset and progressive atrophy of distal muscles caused by motoneuronal degeneration. 31640251 2019
Entrez Id: 9927
Gene Symbol: MFN2
MFN2 		0.110 Biomarker disease HPO