All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02366 CMD-1D;LVNC-6 cardiomyopathy, dilated, type 1D (CMD-1D); ventricular noncompaction, left, type 6 (LVNC-6) 601494 - 0 0 TNNT2 - autosomal dominant
01224 CMH-2 cardiomyopathy, hypertrophic, familial, type 2 (CMH-2) 115195 - 0 0 TNNT2 - -
03137 RCM-3 cardiomyopathy, restrictive, familial, type 3 (RCM-3) 612422 - 0 0 TNNT2 - -
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