Gilbert Syndrome (GILBS)

Alias:

Gilbert Disease

Gilbert's Syndrome

Gilbert Syndrome, Susceptibility to

Meulengracht Syndrome

Gilbert's Disease

Low-Grade Chronic Hyperbilirubinaemia Syndrome

Benign Unconjugated Bilirubinaemia Syndrome

Idiopathic Unconjugated Hyperbilirubinaemia

Hereditary Nonhaemolytic Bilirubinaemia

Chronic Intermittent Juvenile Jaundice

Familial Nonhaemolytic Bilirubinaemia

Constitutional Hyperbilirubinaemia

Constitutional Hepatic Dysfunction

Constitutional Hyperbilirubinemia

Unconjugated Benign Bilirubinemia

Hereditary Nonhaemolytic Jaundice

Hyperbilirubinemia, Gilbert Type

Hereditary Nonhemolytic Jaundice

Constitutional Liver Dysfunction

Familial Nonhaemolytic Jaundice

Hyperbilirubinemia, Arias Type

Familial Nonhemolytic Jaundice

Idiopathic Hyperbilirubinaemia

Icterus Intermittens Juvenilis

Gilbert-Meulengracht Syndrome

Gilbert--Lereboullet Syndrome

Congenital Familial Cholaemia

Gilbert-Lereboullet Syndrome

Cholaemia Familiaris Simplex

Hyperbilirubinaemia Type 1

Physiologic Cholaemia

Hyperbilirubinemia I

Hyperbilirubinemia 1

Meulengracht Icterus

Familial Cholaemia

Gilberts Syndrome

Gilbert Cholaemia

Hblrg

Gilbs

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Gilbert Syndrome, also known as gilbert disease, is related to crigler-najjar syndrome, type ii and glucosephosphate dehydrogenase deficiency. An important gene associated with Gilbert Syndrome is UGT1A1 (UDP Glucuronosyltransferase Family 1 Member A1), and among its related pathways/superpathways are Metabolism and Nuclear receptors meta-pathway. Affiliated tissues include liver and skin, and related phenotypes are unconjugated hyperbilirubinemia and elevated hepatic transaminase

Related ID：

MALACARDS：GLB001

OMIM：143500

MESH：D005878

ICD11：1947520963