Preferred Name |
long QT syndrome |
|
Synonyms |
LQT |
|
Definitions |
OMIM mapping confirmed by DO. [SN]. 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). |
|
ID |
http://purl.obolibrary.org/obo/DOID_2843 |
|
comment |
OMIM mapping confirmed by DO. [SN]. |
|
database_cross_reference |
ICD9CM:426.82 UMLS_CUI:C0035828 MESH:D008133 SNOMEDCT_US_2020_03_01:9651007 OMIM:PS192500 ORDO:101016 SNOMEDCT_US_2020_03_01:20852007 UMLS_CUI:C0023976 ICD10CM:I45.81 GARD:6922 NCI:C34786 ORDO:768 |
|
has exact synonym |
LQT Romano-Ward syndrome long Q-T syndrome |
|
has_alternative_id |
DOID:4069 |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:2843 |
|
imported from | ||
in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/doid#NCIthesaurus http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_FlyBase_slim |
|
label |
long QT syndrome |
|
notation |
DOID:2843 |
|
prefLabel |
long QT syndrome |
|
textual definition |
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). |
|
subClassOf |
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