Disease #01020 (BRGDA5 (Brugada syndrome, type 5 (BRGDA-5, conduction defect, cardiac, nonspecific)), OMIM:612838)

Global Variome shared LOVD

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Official abbreviation	BRGDA5
Name	Brugada syndrome, type 5 (BRGDA-5, conduction defect, cardiac, nonspecific)
OMIM ID	612838
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCN1B
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)

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