Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Gilbert's syndrome
ADR ID BADD_A01826
ADR Hierarchy
03      Congenital, familial and genetic disorders
03.08      Metabolic and nutritional disorders congenital
03.08.05      Inborn errors of bilirubin metabolism
03.08.05.002      Gilbert's syndrome
09      Hepatobiliary disorders
09.01      Hepatic and hepatobiliary disorders
09.01.10      Hepatic metabolic disorders
09.01.10.007      Gilbert's syndrome
14      Metabolism and nutrition disorders
14.14      Inborn errors of metabolism
14.14.05      Inborn errors of bilirubin metabolism
14.14.05.002      Gilbert's syndrome
Description A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level. [MeSH]
MedDRA Code 10018267
MeSH ID D005878
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
Gilbert's syndrome | Gilbert Disease | Disease, Gilbert | Gilbert's Disease | Disease, Gilbert's | Gilberts Disease | Gilbert's Syndrome | Gilberts Syndrome | Syndrome, Gilbert's | Hyperbilirubinemia 1 | Hyperbilirubinemia 1s | Unconjugated Benign Bilirubinemia | Hyperbilirubinemia, Arias Type | Arias Type Hyperbilirubinemia | Arias Type Hyperbilirubinemias | Hyperbilirubinemias, Arias Type | Constitutional Liver Dysfunction | Familial Nonhemolytic Jaundice | Gilbert-Lereboullet Syndrome | Meulengracht Syndrome | Gilbert Syndrome | Syndrome, Gilbert | Hyperbilirubinemia I
ADR Related Proteins
Protein Name UniProt AC TTD Target ID
Not AvailableNot AvailableNot Available
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D00180Atomoxetine0.000992%
BADD_D00809Escitalopram--
BADD_D01253Lenalidomide0.001158%
BADD_D01933Ribavirin0.063458%
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