Jump to:
loading...| Preferred Name |
Short Qt Syndrome |
|
| Synonyms |
|
|
| ID |
http://purl.bioontology.org/ontology/MESH/C580439 |
|
| cui |
C2348199 |
|
| HM |
D001145 |
|
| Inverse of RB |
0 |
|
| Mapped to | ||
| MDA |
20131024 |
|
| MeSH Frequency |
112 |
|
| MMR |
20160707 |
|
| notation |
C580439 |
|
| prefLabel |
Short Qt Syndrome |
|
| SC |
3 |
|
| Scope Statement |
A cardiac CHANNELOPATHY and arrhythmia associated with a predisposition to ATRIAL FIBRILLATION and SUDDEN CARDIAC DEATH. Patients have a structurally normal heart, but electrocardiography (ECG) exhibits abbreviated QTc (Bazett's corrected QT) intervals of less than 360 ms. May be caused by autosomal dominant mutations in the KCNH2 gene. OMIM: 609620 |
|
| TERMUI |
T842447 |
|
| TH |
GHR (2014) |
|
| tui |
T047 |
Create mapping