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Disease association ontology term - MONDO:1010180 - cardiogenetic rhythm disorder

Term summary

ID
MONDO:1010180
Name
cardiogenetic rhythm disorder
Ontology or CV name
Disease association
Definition
Any cardiac rhythm disorder with a monogenic etiology that includes, but is not limited to, atrial fibrillation, sick sinus syndrome, progressive cardiac conduction disease, ventricular fibrillation, Brugada syndrome, long QT syndrome, short QT syndrome, tachycardia with fibrillation.

Parents

Annotation

Disease association

MONDO:0014340 - atrial fibrillation, familial, 15

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MONDO:0015001 - atrial fibrillation, familial, 18

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MONDO:0012728 - Brugada syndrome 2

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MONDO:0013529 - catecholaminergic polymorphic ventricular tachycardia 3

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MONDO:0013966 - catecholaminergic polymorphic ventricular tachycardia 4

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MONDO:0032915 - long QT syndrome 16

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MONDO:0859368 - short QT syndrome 7

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MONDO:0859173 - sick sinus syndrome 4

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MONDO:0013063 - ventricular fibrillation, paroxysmal familial, 2

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