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
02884 CMD1P cardiomyopathy, dilated, type 1P (CMD-1P) 609909 - - - PLN - -
03477 CMH18 cardiomyopathy, hypertrophic, familial, type 18 (CMH-18) 613874 AD - - PLN - -
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