Arrhythmogenic right ventricular dysplasia, familial, 3

Preferred Label : Arrhythmogenic right ventricular dysplasia, familial, 3;

Symbol : ARVD3;

CISMeF acronym : ARVC3; ARVD3;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : ARVC3; Arrhythmogenic right ventricular cardiomyopathy 3;

Description : For phenotypic information and evidence of genetic heterogeneity in this disorder, see ARVD1 (107970).;

Inheritance : Autosomal dominant; Heterogeneity;

Prefixed ID : %602086;

Details

Origin ID

602086;

UMLS CUI

C1865882;

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 3 [DO Concept]
- arrhythmogenic right ventricular dysplasia, familial, 3 [MeSH concept]
- arrhythmogenic right ventricular dysplasia, familial, 3 [MeSH Supplementary Concept]
DO Cross reference
- arrhythmogenic right ventricular dysplasia 3 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Focal necrosis of right ventricular muscle cells [HPO term]
- Heterogeneous [HPO term]
- Right ventricular cardiomyopathy [HPO term]
- T-wave inversion in the right precordial leads [HPO term]
- Ventricular arrhythmia [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, 3 [MeSH Supplementary Concept]
- arrhythmogenic right ventricular dysplasia, familial, 3 [MeSH concept]

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