MFN2, mitofusin 2, 9927

N. diseases: 334; N. variants: 75
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
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
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
0.020 Biomarker disease BEFREE CMT2A is primarily an axonal disorder resulting in motor and sensory neuropathy. 26307494 2015