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
03629 CMYO10A;EMARDD myopathy, congenital, type 10A, severe variant 614399 AR 2 3 MEGF10 - -
07258 CMYO10B myopathy, congenital, type 10B, mild variant 620249 AR - - MEGF10 - -
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