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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
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| Id | http://purl.bioontology.org/ontology/NDFRT/N0000010987
http://purl.bioontology.org/ontology/NDFRT/N0000010987
|
|---|---|
| Preferred Name | Long QT Syndrome [Disease/Finding] |
| Synonyms |
Long QT Syndrome
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Long QT Syndrome
|
|---|---|
| prefLabel |
Long QT Syndrome [Disease/Finding]
|
| notation |
N0000010987
|
| MESH 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.
|
| MESH UI |
M0012684
|
| subClassOf | |
| Semantic type UMLS property | |
| MeSH name |
Long QT Syndrome
|
| NDFRT kind |
DISEASE_KIND
|
| type | |
| SNOMED CID |
9651007
|
| tui |
T047
|
| NUI |
N0000010987
|
| cui |
C0023976
|
| MESH DUI |
D008133
|
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