Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
General Information (adopted from Orphanet):
|
Synonyms, Signs:
|
Familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form
|
|
Number of Symptoms
|
0
|
|
OrphanetNr:
|
293899
|
|
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) |
|
|
|
|
|
|
|
|
|
ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |