Catecholaminergic polymorphic ventricular tachycardia

disorder

SNOMED 419671004CUI C5574922

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Ventricular tachycardia

Very frequent (80-99%)HP:0004756

Dizziness

Frequent (30-79%)HP:0002321

Heart stops beating

Frequent (30-79%)HP:0001695

Palpitations

Frequent (30-79%)HP:0001962

Polymorphic ventricular tachycardia

Frequent (30-79%)HP:0031677

Quivering upper heart chambers resulting in irregular heartbeat

Frequent (30-79%)HP:0005110

Supraventricular tachyarrhythmia

Frequent (30-79%)HP:0004755

Sudden cardiac death

Occasional (5-29%)HP:0001645

Syncope

Occasional (5-29%)HP:0001279

Ventricular fibrillation

Occasional (5-29%)HP:0001663

Related Conditions

Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation(child)

Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation(child)

Ventricular tachycardia, polymorphic(parent)

Cardiac channelopathy(parent)

Tachyarrhythmia(parent)

Quick Facts

SNOMED CT: 419671004
UMLS CUI: C5574922
Fully Specified Name: Catecholaminergic polymorphic ventricular tachycardia (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.