Disease #03951 (CPVT5 (tachycardia, ventricular, catecholaminergic polymorphic, type 5, with/without muscle weakness), OMIM:615441)

Official abbreviation CPVT5
Name tachycardia, ventricular, catecholaminergic polymorphic, type 5, with/without muscle weakness
OMIM ID 615441
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TRDN
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00080953 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - CPVT5 Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness (OMIM:615441) TRDN TRDN 1 1 Daniel Trujillano
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