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
01926 MEOAL;MMDS8 mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy 251900 AR 44 43 FDX1L - -
00244 MYOP myopathy (MYOP) - - 947 878 FDX1L, FXR1, JPH1, MLIP, MYL1, NDUFAF7, PLIN4 - -
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