Wolff-parkinson-white syndrome

Preferred Label : Wolff-parkinson-white syndrome;

Symbol : WPW;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Wpw syndrome;

Included titles and symbols : Preexcitation syndrome; Accessory atrioventricular pathways;

Inheritance : Autosomal dominant;

Molecular basis : Due to mutation in the protein kinase AMP-activated non-catalytic subunit gamma 2 gene (PRKAG2, 602743.0001);

Prefixed ID : #194200;

Details

Origin ID

194200;

UMLS CUI

C0043202;

Automatic exact mappings (from CISMeF team)
- Accelerated atrioventricular conduction (disorder) [SNOMED CT concept]
- Structure of accessory atrioventricular bundle (body structure) [SNOMED CT concept]
- Wolff-Parkinson-White Syndrome, CTCAE [NCIt concept]
- accessory atrioventricular bundle [MeSH Descriptor]
Currated CISMeF NLP mapping
- Pre-Excitation Syndrome [NCIt concept]
- Pre-Excitation syndromes [MeSH concept]
- Pre-excitation syndrome [ICD-10 Sub-category]
- Pre-excitation syndrome [MedDRA LLT]
- Pre-excitation syndrome [ICD-10 Sub-category (who)]
- Ventricular preexcitation [HPO term]
- WPW syndrome [MedDRA LLT]
- Wolff Parkinson White syndrome [Disease (Nov.)]
- Wolff-Parkinson-White Syndrome [NCIt concept]
- Wolff-Parkinson-White pattern (disorder) [SNOMED CT concept]
- Wolff-Parkinson-White syndrome [PASCAL descriptor]
- Wolff-Parkinson-White syndrome [HPO term]
- Wolff-Parkinson-White syndrome [DO Concept]
- Wolff-Parkinson-White syndrome [ICD-11 Subcategory]
- Wolff-Parkinson-White syndrome [MedDRA Preferred Term]
- Wolff-Parkinson-White syndrome [MeSH concept]
- Wolff-Parkinson-White syndrome [ORDO Disease]
- Wolff-Parkinson-White syndrome acquired [MedDRA LLT]
- pre-excitation syndromes [MeSH Descriptor]
- wolff-parkinson-white syndrome [MeSH Descriptor]
- wolff-parkinson-white syndrome [SNOMED Notion]
DO Cross reference
- Wolff-Parkinson-White syndrome [DO Concept]
Genes related to phenotype
- Protein kinase, amp-activated, noncatalytic, gamma-2 [OMIM gene]
HPO term(s)
- Atrial flutter [HPO term]
- Autosomal dominant inheritance [HPO term]
- Childhood onset [HPO term]
- Juvenile onset [HPO term]
- Palpitations [HPO term]
- Paroxysmal atrial fibrillation [HPO term]
- Prolonged QRS complex [HPO term]
- Shortened PR interval [HPO term]
- Sudden cardiac death [HPO term]
- Syncope [HPO term]
- Ventricular preexcitation [HPO term]
- Ventricular preexcitation with multiple accessory pathways [HPO term]
- Wolff-Parkinson-White syndrome [HPO term]
- Young adult onset [HPO term]
ORDO concept(s)
- Wolff-Parkinson-White syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- WPW syndrome [MedDRA LLT]
- Wolff-Parkinson-White Syndrome [NCIt concept]
- Wolff-Parkinson-White pattern (disorder) [SNOMED CT concept]
- Wolff-Parkinson-White syndrome [ORDO Disease]
- Wolff-Parkinson-White syndrome [MeSH concept]
- Wolff-Parkinson-White syndrome [MedDRA Preferred Term]
- Wolff-Parkinson-White syndrome [HPO term]
- Wolff-Parkinson-White syndrome congenital [MedDRA Preferred Term]
- wolff-parkinson-white syndrome [SNOMED Notion]
- wolff-parkinson-white syndrome [MeSH Descriptor]
Validated automatic mappings to NTBT
- preexcitation syndrome [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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