All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02786 CMH-8 cardiomyopathy, hypertrophic, familial, type 8 (CMH-8) 608751 0 0 MYL3 - -