Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)

Alias:
Cpvt
Bidirectional Ventricular Tachycardia Induced by Catecholamine
Polymorphic Ventricular Tachycardia Induced by Catecholamines
Catecholamine-Induced Polymorphic Ventricular Tachycardia
Malignant Paroxysmal Ventricular Tachycardia
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1
Ventricular Tachycardia, Catecholaminergic Polymorphic
Bidirectional Tachycardia Induced by Catecholamines
Stress-Induced Polymorphic Ventricular Tachycardia
Familial Polymorphic Ventricular Tachycardia
Multifocal Premature Ventricular Beats
Familial Ventricular Tachycardia
Multifocal Pvcs
Fpvt
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Catecholaminergic Polymorphic Ventricular Tachycardia, also known as cpvt, is related to ventricular tachycardia, catecholaminergic polymorphic, 3 and ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy, and has symptoms including seizures and syncope. An important gene associated with Catecholaminergic Polymorphic Ventricular Tachycardia is CASQ2 (Calsequestrin 2), and among its related pathways/superpathways are Activation of cAMP-Dependent PKA and CREB Pathway. The drugs Calcium, Dietary and Calcium have been mentioned in the context of this disorder. Affiliated tissues include heart and cardiac myocytes, and related phenotypes are ventricular tachycardia and vertigo
Related ID:
ICD11:976309888

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Child
1-5/10000
57
497
96

Medical Symptom

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Description
HPO Frequency
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HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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MGI
Related Gene
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Publications
No data available

References Literature

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