Disease #03344 (LQT13 (QT syndrome, long, type 13 (LQT-13)), OMIM:613485)

Official abbreviation LQT13
Name QT syndrome, long, type 13 (LQT-13)
OMIM ID 613485
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene KCNJ5
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

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00054786 - PubMed: Yang 2010 4-generation family, 10 affecteds (7F, 3M) - - China - - - - - LQT13 - KCNJ5 KCNJ5 1 10 Frans Cremers
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