All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03544 ASD3 septal defect, atrial, type 3 614089 - - - MYH6 - -
03293 CMD1EE cardiomyopathy, dilated, type 1EE 613252 - - - MYH6 - -
00351 CMH cardiomyopathy, hypertrophic (CMH) - - 1667 1621 MYH6, RPS6KB1, TCAP - -
03292 CMH14 cardiomyopathy, hypertrophic, familial, type 14 613251 AD - - MYH6 - -
03545 SSS3 sinus, sick, syndrome, type 3, susceptibility to 614090 - 3 1 MYH6 - -
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