Disease #00158 (SHORT QT SYNDROME (SHORT QT SYNDROME 2), OMIM:609621)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	SHORT QT SYNDROME
Name	SHORT QT SYNDROME 2
OMIM ID	609621
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KCNQ1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-27 10:49:29 +00:00 (UTC)
Date last edited	N/A