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Start free with EleplanCalmodulin-related catecholaminergic polymorphic ventricular tachycardia
ORPHA:730657Etiological subtype
Also called Calmodulin-related CPVT · Calmodulin-related malignant paroxysmal ventricular tachycardia · Calmodulin-related polymorphic ventricular tachycardia induced by catecholamines · Calmodulin-related bidirectional ventricular tachycardia induced by catecholamines
What it is
Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.
Key facts
- Inheritance
- Autosomal dominant
- Classified as
- Etiological subtype
Recorded for the broader condition
- Prevalence
- 1-5 / 10 000 (Europe)Catecholaminergic polymorphic ventricular tachycardia
- Age of onset
- Adolescent, Adult, ChildhoodCatecholaminergic polymorphic ventricular tachycardia
Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.
Genes
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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