VENTRICULAR TACHYCARDIA, FAMILIAL

General Information (adopted from Orphanet):

Synonyms, Signs: VENTRICULAR TACHYCARDIA, FAMILIAL POLYMORPHIC
Number of Symptoms 9
OrphanetNr:
OMIM Id: 192605
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0001638) Cardiomyopathy 192 / 7739
2
(HPO:0004751) Paroxysmal ventricular tachycardia 5 / 7739
3
(HPO:0001637) Abnormality of the myocardium 76 / 7739
4
(HPO:0001645) Sudden cardiac death 84 / 7739
5
(HPO:0001939) Abnormality of metabolism/homeostasis 328 / 7739
6
(OMIM) No metabolic disorder 1 / 7739
7
(OMIM) No repolarization abnormality 1 / 7739
8
(OMIM) Right bundle branch block with left axis deviation on EKG 1 / 7739
9
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: