All diseases associated with gene MFN2

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated tissues

Disease features
00014 HMSN Hereditary Sensory and Motor Neuropathy - - 245 - - -
00027 OPA Optic Atrophy 165500 - 296 - - -
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