All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06997 MMCKR myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 620138 AR - - MLIP - myopathy, myalgia, increased serum creatine kinase, with/without episodic rhabdomyolysis
00244 MYOP myopathy (MYOP) - - 1058 989 FDX1L, FXR1, JPH1, MLIP, MYL1, NDUFAF7, PLIN4 - -
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