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
01226 CMH4 cardiomyopathy, hypertrophic, familial, type 4 (CMH-4) 115197 AD;AR 1 1 MYBPC3 - -
03924 LVNC10;CMD1MM ventricular noncompaction, left, type 10 (LVNC-10, cardiomyopathy, dilated, type 1MM (CMD-1MM)) 615396 AD 1 1 MYBPC3 - -
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