ORPHA:730728
Catecholaminergic polymorphic ventricular tachycardia without known causative genetic defect
Synonyms: Malignant paroxysmal ventricular tachycardia without known causative genetic defect · Polymorphic ventricular tachycardia without known causative genetic defect · Bidirectional ventricular tachycardia without known causative genetic defect · CPVT without known causative genetic defect
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Inheritance
- Unknown
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Catecholaminergic polymorphic ventricular tachycardia without known causative genetic defect | Malignant paroxysmal ventricular tachycardia without known causative genetic defect · Polymorphic ventricular tachycardia without known causative genetic defect · Bidirectional ventricular tachycardia without known causative genetic defect · CPVT without known causative genetic defect |
| fr | Tachycardie ventriculaire polymorphe catécholaminergique sans anomalie génétique causale connue | Tachycardie ventriculaire bidirectionnelle induite par les catécholamines sans anomalie génétique causale connue · Tachycardie ventriculaire paroxystique maligne sans anomalie génétique causale connue · TVPC sans anomalie génétique causale connue · Tachycardie ventriculaire polymorphe induite par les catécholamines sans anomalie génétique causale connue |
| de | Katecholaminerge polymorphe ventrikuläre Tachykardie ohne bekannten ursächlichen Gendefekt | CPVT ohne bekannten ursächlichen Gendefekt · Polymorphe ventrikuläre Tachykardie ohne bekannten ursächlichen Gendefekt · Bidirektionale ventrikuläre Tachykardie ohne bekannten ursächlichen Gendefekt · Maligne paroxysmale ventrikuläre Tachykardie ohne bekannten ursächlichen Gendefekt |
| es | Taquicardia ventricular polimórfica catecolaminérgica sin defecto genético causante conocido | CPVT sin defecto genético causante conocido · Taquicardia ventricular bidireccional sin defecto genético causante conocido · Taquicardia ventricular paroxística maligna sin defecto genético causante conocido · Taquicardia ventricular polimórfica sin defecto genético causante conocido · TVPC sin defecto genético causante conocido |
| it | Tachicardia ventricolare polimorfa catecolaminergica senza difetto genetico noto | CPVT senza difetto genetico noto · Tachicardia ventricolare polimorfa senza difetto genetico noto · Tachicardia ventricolare bidirezionale senza difetto genetico noto · Tachicardia ventricolare parossistica maligna senza difetto genetico noto |
| nl | Catecholaminerge polymorfe ventriculaire tachycardie zonder bekend causaal genetisch defect | Maligne paroxismale ventriculaire tachycardie zonder bekend causaal genetisch defect · Bidirectionele ventriculaire tachycardie zonder bekend causaal genetisch defect · Polymorfe ventriculaire tachycardie zonder bekend causaal genetisch defect · CPVT zonder bekend causaal genetisch defect |
| pt | Catecholaminergic polymorphic ventricular tachycardia without known causative genetic defect | |
| pl | Catecholaminergic polymorphic ventricular tachycardia without known causative genetic defect | = en |
| cs | Catecholaminergic polymorphic ventricular tachycardia without known causative genetic defect | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:3286Catecholaminergic polymorphic ventricular tachycardia
rare cardiac diseases; rare genetic diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/730728
- This record as JSON: /data/d/730728.json