Disease #00216 (LQT3 (LONG QT SYNDROME 3), OMIM:603830)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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	Curators: Florian Bayersdorfer and Sabine Heber

Official abbreviation	LQT3
Name	LONG QT SYNDROME 3
OMIM ID	603830
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SCN5A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-09-09 09:44:34 +00:00 (UTC)
Date last edited	N/A