All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03458 CMH16 cardiomyopathy, hypertrophic, familial, type 16 (CMH-16) 613838 - - - MYOZ2 - autosomal dominant
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