All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02709 CMT2K Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K 607831 AD;AR 7 5 GDAP1, JPH1 - -
07250 CMYO25 myopathy, congenital, type 25 620964 AR - - JPH1 - -
00244 MYOP myopathy (MYOP) - - 1388 1319 FDX1L, FXR1, JPH1, MLIP, MYL1, NDUFAF7, PLIN4 - -
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