All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01462 CMYO2A;NEM3 myopathy, congenital, type 2A, typical 161800 AD 201 200 ACTA1 - -
07099 CMYO2B myopathy, congenital, type 2B, severe infantile 620265 AR - - ACTA1 - -
07100 CMYO2C myopathy, congenital, type 2C, severe infantile 620278 AD - - ACTA1 - -
06005 SHPM myopathy, scapulohumeroperoneal 616852 AD - - ACTA1 - -
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