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
01613 - Wolff-Parkinson-White pattern 194200 AD - - PRKAG2 - -
02013 - storage disease, glycogen, type of heart, lethal congenital 261740 AD - - PRKAG2 - -
02319 CMH6 cardiomyopathy, hypertrophic, familial, type 6 (CMH-6) 600858 AD - - PRKAG2 - -
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