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
03266 CMD1CC cardiomyopathy, dilated, type 1CC (CMD-1CC) 613122 AD - - NEXN - -
03479 CMH20 cardiomyopathy, hypertrophic, familial, type 20 (CMH-20) 613876 AD - - NEXN - -
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