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
02663 CMD1M cardiomyopathy, dilated, type 1M (CMD-1M) 607482 - - - CSRP3 - -
03091 CMH12 cardiomyopathy, hypertrophic, familial, type 12 (CMH-12) 612124 AD - - CSRP3 - -
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