About: long QT syndrome

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	intrinsic cardiomyopathy nodeID://b50951232
label	long QT syndrome
comment	OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:2843
has_alternative_id	DOID:4069
database_cross_reference	ORDO:768 GARD:6922 ICD10CM:I45.81 ICD9CM:426.82 MESH:D008133 NCI:C34786 OMIM:PS192500 ORDO:101016 SNOMEDCT_US_2021_09_01:9651007 UMLS_CUI:C0023976
has_exact_synonym	LQT (en) Romano-Ward syndrome (en) long Q-T syndrome (en)
has_obo_namespace	disease_ontology
in_subset	DO_FlyBase_slim NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles).
is subClassOf of	Jervell-Lange Nielsen syndrome Andersen-Tawil syndrome long QT syndrome 1 long QT syndrome 2 long QT syndrome 3 long QT syndrome 5 long QT syndrome 6 long QT syndrome 9 long QT syndrome 10 long QT syndrome 11 long QT syndrome 12 long QT syndrome 13 long QT syndrome 14 long QT syndrome 15 long QT syndrome 4
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50951233

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