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
04015 - Rienhoff syndrome 615582 - - - TGFB3 - -
01182 ARVD-1;ARVC-1 dysplasia, arrhythmogenic right ventricular, type 1 (ARVD-1, arrhythmogenic right ventricular cardiomyopathy (ARVC-1)) 107970 - - - TGFB3 - -
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