Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Long QT syndrome congenital
ADR ID BADD_A05537
ADR Hierarchy
03      Congenital, familial and genetic disorders
03.07      Cardiac and vascular disorders congenital
03.07.07      Cardiac disorders congenital NEC
03.07.07.002      Long QT syndrome congenital
02      Cardiac disorders
02.03      Cardiac arrhythmias
02.03.01      Cardiac conduction disorders
02.03.01.019      Long QT syndrome congenital
Description A form of long QT syndrome that is without congenital deafness. It is caused by mutation of the KCNQ1 gene which encodes a protein in the VOLTAGE-GATED POTASSIUM CHANNEL. [MeSH]
MedDRA Code 10057926
MeSH ID D029597; D029593
ADR Severity Grade (FAERS) Not Available
ADR Severity Grade (CTCAE) Not Available
Synonym
Romano Ward syndrome | Long QT syndrome congenital | Jervell and Lange-Nielsen syndrome | Romano-Ward Syndrome | Romano Ward Syndrome | Syndrome, Romano-Ward | Ventricular Fibrillation with Prolonged QT Interval | Long QT Syndrome Type 1 | Long QT Syndrome 1 | Ward-Romano Syndrome | Syndrome, Ward-Romano | Ward Romano Syndrome
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D01951Risperidone--
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