Arrhythmogenic right ventricular dysplasia, familial, 6

Preferred Label : Arrhythmogenic right ventricular dysplasia, familial, 6;

Symbol : ARVD6;

CISMeF acronym : ARVC6; ARVD6;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : ARVC6; Arrhythmogenic right ventricular cardiomyopathy 6;

Description : For a phenotypic description and a discussion of genetic heterogeneity of this disorder, see ARVD1 (107970).;

Prefixed ID : %604401;

Détails

Origin ID

604401;

UMLS CUI

C1858378;

Automatic exact mappings (from CISMeF team)
- Familial isolated arrhythmogenic right ventricular dysplasia [ORDO Disease]
Broader ORDO disease(s)
- Arrhythmogenic right ventricular cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- arrhythmogenic right ventricular dysplasia 6 [DO Concept]
- arrhythmogenic right ventricular dysplasia, familial, 6 [MeSH concept]
- arrhythmogenic right ventricular dysplasia, familial, 6 [MeSH Supplementary Concept]
DO Cross reference
- arrhythmogenic right ventricular dysplasia 6 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Premature ventricular contraction [HPO term]
- Right ventricular cardiomyopathy [HPO term]
- Sudden cardiac death [HPO term]
ORDO concept(s)
- Familial isolated arrhythmogenic right ventricular dysplasia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- arrhythmogenic right ventricular dysplasia, familial, 6 [MeSH Supplementary Concept]
- arrhythmogenic right ventricular dysplasia, familial, 6 [MeSH concept]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients