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
02523 CPVT1 tachycardia, ventricular, catecholaminergic polymorphic, type 1 (CPVT-1) 604772 AD 136 136 CASQ2, RYR2, TRDN - -
03951 CPVT5 tachycardia, ventricular, catecholaminergic polymorphic, type 5, with/without muscle weakness 615441 AR 1 1 TRDN - -
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