Arrhythmogenic right ventricular dysplasia, familial, 2

Preferred Label : Arrhythmogenic right ventricular dysplasia, familial, 2;

Obsolete resource : true;

Moved to : 604772;

Symbol : ARVD2;

CISMeF acronym : ARVC2; ARVD2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Arrhythmogenic right ventricular cardiomyopathy 2; ARVC2;

Inheritance : Autosomal dominant; heterogeneity.;

Prefixed ID : 600996;

Détails

Origin ID

600996;

UMLS CUI

C1832931;

Automatic exact mappings (from CISMeF team)
- Familial isolated arrhythmogenic right ventricular dysplasia [ORDO Disease]
- ryanodine receptor 2 [ORDO Gene]
Broader ORDO disease(s)
- Arrhythmogenic right ventricular cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- arrhythmogenic right ventricular dysplasia 2 [DO Concept]
- arrhythmogenic right ventricular dysplasia, familial, 2 [MeSH concept]
- arrhythmogenic right ventricular dysplasia, familial, 2 [MeSH Supplementary Concept]
DO Cross reference
- arrhythmogenic right ventricular dysplasia 2 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Dilatation of the ventricular cavity [HPO term]
- Effort-induced polymorphic ventricular tachycardia [HPO term]
- Right ventricular cardiomyopathy [HPO term]
- Sudden death [HPO term]
ORDO concept(s)
- Familial isolated arrhythmogenic right ventricular dysplasia [ORDO Disease]
- Familial isolated arrhythmogenic ventricular dysplasia, right dominant form [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- arrhythmogenic right ventricular dysplasia, familial, 2 [MeSH Supplementary Concept]
- arrhythmogenic right ventricular dysplasia, familial, 2 [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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