Gene: MFN2 ×
Source: BEFREE ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9927
Gene Symbol: MFN2
MFN2 		0.020 GeneticVariation disease BEFREE Mutations in the Mitofusin 2 (MFN2) gene have been identified in patients with autosomal dominant axonal motor and sensory neuropathy or Charcot-Marie-Tooth 2A (CMT2A). 30011089 2018
Entrez Id: 9927
Gene Symbol: MFN2
MFN2 		0.020 Biomarker disease BEFREE CMT2A is primarily an axonal disorder resulting in motor and sensory neuropathy. 26307494 2015