Preferred Name |
long QT syndrome |
|
Synonyms |
LQT long Q-T syndrome |
|
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 GARD:6922 ICD10CM:I45.81 ORDO:768 OMIM:PS192500 SNOMEDCT_US_2021_09_01:9651007 UMLS_CUI:C0023976 MESH:D008133 NCI:C34786 ORDO:101016 |
|
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). |
|
has_alternative_id |
DOID:4069 |
|
has_exact_synonym |
LQT Romano-Ward syndrome long Q-T syndrome |
|
has_obo_namespace |
disease_ontology |
|
has_symptom | ||
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). |
|
id |
DOID:2843 |
|
in_subset | ||
label |
long QT syndrome |
|
notation |
DOID:2843 |
|
prefLabel |
long QT syndrome |
|
subClassOf |