Details of Disease

General Information of Disease (ID: DISOPLNU)

Disease Name Catecholaminergic polymorphic ventricular tachycardia 3
Synonyms
ventricular tachycardia, catecholaminergic polymorphic, 3; CPVT3; TECRL catecholaminergic polymorphic ventricular tachycardia; catecholaminergic polymorphic ventricular tachycardia type 3; catecholaminergic polymorphic ventricular tachycardia 3; catecholaminergic polymorphic ventricular tachycardia caused by mutation in TECRL; CVPT3
Definition Any catecholaminergic polymorphic ventricular tachycardia in which the cause of the disease is a mutation in the TECRL gene.
Disease Hierarchy
DISSAS1A: Catecholaminergic polymorphic ventricular tachycardia
DISOPLNU: Catecholaminergic polymorphic ventricular tachycardia 3
Disease Identifiers
MONDO ID
MONDO_0013529
UMLS CUI
C3151463
OMIM ID
614021
MedGen ID
462813

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
TECRL OTXLSNCP Definitive Autosomal recessive [1]
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References

1 Life-threatening arrhythmias with autosomal recessive TECRL variants. Europace. 2021 May 21;23(5):781-788. doi: 10.1093/europace/euaa376.