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

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