All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00181 CMYO6;MYPOP myopathy, congenital, type 6, with ophthalmoplegia 605637 AD;AR 11 11 MYH2 - -
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