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Disease Browser
Parent Node: Diseases (C)
Parent Node: Polymorphic catecholergic ventricular tachycardia (C536334)
..Starting node ..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3 (OMIM:614021)
Child Nodes:
Sister Nodes:
..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY (OMIM:604772)
..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 (OMIM:611938)
..VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3 (OMIM:614021)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

11574

Name:

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3

Definition:

Alternative IDs:

ParentIDs:

MESH:C536334

TreeNumbers:

C14.280.067.845.940/C536334/614021 |C23.550.073.845.940/C536334/614021

Synonyms:

CPVT3

Slim Mappings:

Cardiovascular disease|Pathology (process)

Reference:

MedGen: 614021
MeSH: 614021
OMIM: 614021;

Genes:

Phenotypes

1	HP:0000007	Autosomal recessive inheritance
2	HP:0001699	Sudden death
3	HP:0001279	Syncope
4	HP:0004756	Ventricular tachycardia

Disease Causing ClinVar Variants