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 		0.310 GeneticVariation disease BEFREE Complex phenotypes have been described in association with MFN2 gene mutations, including CMT2 with pyramidal features (hereditary motor and sensory neuropathy [HSMN V]) and CMT2 with optic atrophy (HMSN VI). 18946002 2008
Entrez Id: 9927
Gene Symbol: MFN2
MFN2 		0.310 GermlineCausalMutation disease ORPHANET