All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05038 CCDD cardiac conduction disease? with/without dilated cardiomyopathy (CCDD) 616117 AD - - TNNI3K - -
03300 CMD1FF cardiomyopathy, dilated, type 1FF (CMD-1FF) 613286 - - - TNNI3 - -
03069 CMD2A cardiomyopathy, dilated, type 2A (CMD-2A) 611880 AR - - TNNI3 - -
03392 CMH7 cardiomyopathy, hypertrophic, familial, type 7 (CMH-7) 613690 AD - - TNNI3 - -
01228 RCM1 cardiomyopathy, restrictive, familial, type 1 (RCM-1) 115210 AD - - TNNI3 - -
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