ADR Ontology |
ADR Term |
Long QT syndrome |
ADR ID |
BADD_A02576 |
ADR Hierarchy |
|
Description |
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] |
MedDRA Code |
10024803 |
MeSH ID |
D008133
|
ADR Severity Grade (FAERS)
|
|
ADR Severity Grade (CTCAE)
|
Not Available
|
Synonym |
Long QT syndrome | Long QT Syndrome |
|
|
ADR Related Proteins |
Protein Name |
UniProt AC |
TTD Target ID |
Not Available | Not Available | Not Available |
|
Drugs Leading to the ADR |
|