Disease #00181 (LQT2 (LONG QT SYNDROME 2), OMIM:613688)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	LQT2
Name	LONG QT SYNDROME 2
OMIM ID	613688
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KCNH2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-30 09:43:57 +00:00 (UTC)
Date last edited	N/A