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
02912 ARVD10 dysplasia, ventricular, right, arrhythmogenic, type 10 (ARVD-10) 610193 AD - - DSG2 - -
03199 CMD1BB cardiomyopathy, dilated, type 1BB (CMD-1BB) 612877 - - - DSG2 - -
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