Disease #00183 (LQT13 (LONG QT SYNDROME 13), OMIM:613485)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	LQT13
Name	LONG QT SYNDROME 13
OMIM ID	613485
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KCNJ5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-30 10:09:33 +00:00 (UTC)
Date last edited	N/A