Disease #00180 (LQT5 (LONG QT SYNDROME 5), OMIM:613695)

Official abbreviation LQT5
Name LONG QT SYNDROME 5
OMIM ID 613695
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene KCNE1
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-29 13:37:51 +00:00 (UTC)
Date last edited N/A

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