Disease #00222 (LQT8 (LONG QT SYNDROME 8), OMIM:618447)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	LQT8
Name	LONG QT SYNDROME 8
OMIM ID	618447
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CACNA1C
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-09-09 10:55:47 +00:00 (UTC)
Date last edited	N/A