Disease #05143 (CPVT3 (tachycardia, ventricular, catecholaminergic polymorphic, type 3), OMIM:614021)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CPVT3
Name	tachycardia, ventricular, catecholaminergic polymorphic, type 3
OMIM ID	614021
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TECRL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-03-20 12:03:11 +01:00 (CET)
Date last edited	2025-11-19 14:23:25 +01:00 (CET)

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