Disease #00406 (LQT5 (QT syndrome, long, type 5 (LQT-5)), OMIM:613695)

Official abbreviation LQT5
Name QT syndrome, long, type 5 (LQT-5)
OMIM ID 613695
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 KCNE1
Associated tissues -
Disease features -
Remarks -
Date created 2014-06-06 19:16:12 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00004255 - PubMed: Riuro 2014 - - - - - - - - - LQT5 - KCNE1, KCNE2, KCNH2, KCNQ1, SCN5A KCNE1 1 1 Anna Iglesias
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