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Medical Subject Headings
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/MESH/D008133
http://purl.bioontology.org/ontology/MESH/D008133
|
|---|---|
| Preferred Name | Long QT Syndrome |
| Definitions |
A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME.
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| Synonyms |
Electrocardiogram QT Prolonged
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME. |
|---|---|
| altLabel | Electrocardiogram QT Prolonged
|
| prefLabel | Long QT Syndrome
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| Machine permutation | 1991; see ARRHYTHMIA 1986-1990
|
| HN | 1991(1986); use ARRHYTHMIA 1986-1990
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| Mapped from |
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| type | |
| tui |
T047
T033
|
| TERMUI |
T000957215
T024261
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| TH |
NLM (2020)
NLM (1986)
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| MMR | 20190617
|
| notation | D008133
|
| Inverse of RO | |
| Semantic type UMLS property | |
| Inverse of AQ |
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|
| DX | 19910101
|
| cui |
C0023976
C0151878
|
| DC | 1
|
| MN |
C23.550.073.547
C14.280.123.625
C14.280.067.565
C16.131.240.400.715
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| AQL | BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
|
| MDA | 19990101
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |