Familial isolated arrhythmogenic ventricular dysplasia, right dominant form

General Information (adopted from Orphanet):

Synonyms, Signs: Familial isolated arrhythmogenic ventricular dysplasia, classic form
Familial isolated arrhythmogenic ventricular cardiomyopathy, classic form
Familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form
Number of Symptoms 0
OrphanetNr: 293910
OMIM Id:
ICD-10: I42.8
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Familial isolated arrhythmogenic right ventricular dysplasia
 -Rare cardiac disease
 -Rare genetic disease

Comment:

This disease is described in Familial isolated arrhythmogenic right ventricular dysplasia (Orphanet:217656, Phenodis:2263)

Symptom Information: Sort by abundance 

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: