Disease #02864 (SQT3 (QT syndrome, short, type 3 (SQT-3)), OMIM:609622)

Official abbreviation SQT3
Name QT syndrome, short, type 3 (SQT-3)
OMIM ID 609622
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene KCNJ2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00206660 - PubMed: Priori 2005 PubMed: El Harchi 2009 cardiac abnormalities F ? Italy - >5y - - - SQT3 short QT syndrome, narrow and peaked T waves KCNJ2 KCNJ2 1 2 Ikuko Takeda
00206696 - PubMed: Deo 2013 cardiac abnormalities M ? Italy - >11y - - - SQT3 paroxysmal AF, mild left ventricular dysfunction, short QT syndrome KCNJ2 KCNJ2 1 1 Ikuko Takeda
00206704 - PubMed: Hattori 2012 cardiac abnormalities F ? Japan Japanese >8y - - - SQT3 shortened QT interval, paroxysmal AF, VF inducibility, mental retardation, abnormal proliferation of oesophageal blood vessels, epilepsy, Kawasaki disease KCNJ2 KCNJ2 1 1 Ikuko Takeda
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