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
00244 MYOP myopathy (MYOP) - - 726 658 FDX1L, FXR1, MYL1, NDUFAF7 - -
06601 MYOPMIL ?Myopathy, congenital proximal, with minicore lesions 618823 AR 0 0 FXR1 - -
06600 MYORIBF ?Myopathy, congenital, with respiratory insufficiency and bone fractures 618822 AR 0 0 FXR1 - -
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