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3 entries on 1 page. Showing entries 1 - 3.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00488 CMT2A2 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2 609260 0 0 MFN2 - -
00485 HSMN6 NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VI; HSMN6 601152 0 0 MFN2 - -
00494 MSL LIPOMATOSIS, MULTIPLE SYMMETRIC; MSL 151800 0 0 MFN2 - -