All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00351 CMH cardiomyopathy, hypertrophic (CMH) - - 1667 1621 MYH6, RPS6KB1, TCAP - -
02667 CMH25 cardiomyopathy, hypertrophic, type 25 (CMD-25) 607487 AD - - TCAP - autosomal dominant
05126 LGMD dystrophy, muscular, limb-girdle (LGMD) - - 7500 3655 POPDC3, TCAP, TRAPPC11 - -
02405 LGMDR7;LGMD2G dystrophy, muscular, limb-girdle, type 2G 601954 AR 2 2 TCAP - -
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