All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01596 CMH-1 cardiomyopathy, hypertrophic, familial, type 1 (CMH-1) 192600 - 0 0 CAV3, MYH6, MYH7, MYLK2 - -
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