loading...| Preferred Name | long QT syndrome | |
| Synonyms |
Romano-Ward syndrome LQT long Q-T syndrome |
|
| Definitions |
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). OMIM mapping confirmed by DO. [SN]. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_2843 |
|
| comment |
OMIM mapping confirmed by DO. [SN]. |
|
| alternative label |
Romano-Ward syndrome LQT long Q-T syndrome |
|
| database_cross_reference |
ICD9CM:426.82 MESH:D008133 SNOMEDCT_US_2023_03_01:9651007 MIM:PS192500 UMLS_CUI:C0023976 ICD10CM:I45.81 GARD:6922 NCI:C34786 ORDO:768 |
|
| 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). OMIM mapping confirmed by DO. [SN]. |
|
| has exact synonym |
LQT long Q-T syndrome |
|
| has narrower match |
ORDO:101016 |
|
| has symptom | ||
| has_alternative_id |
DOID:4069 |
|
| has_narrow_synonym |
Romano-Ward syndrome |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:2843 |
|
| in_subset |
http://purl.obolibrary.org/obo/doid#NCIthesaurus |
|
| label |
long QT syndrome |
|
| notation |
DOID:2843 |
|
| note |
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). OMIM mapping confirmed by DO. [SN]. |
|
| preferred label |
long QT syndrome |
|
| prefLabel |
long QT syndrome |
|
| subClassOf |