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bn:02541140n
Noun Concept
Categories: Articles requiring reliable medical sources, Heme metabolism disorders, Rare syndromes, All articles needing additional references, Hepatology
EN
Crigler–Najjar syndrome  Crigler-Najjar syndrome  Crigler-Najjar syndrome, type I  Arias syndrome  Bilirubin UDP glucuronyl transferase deficiency
EN
Crigler–Najjar syndrome is a rare inherited disorder affecting the metabolism of bilirubin, a chemical formed from the breakdown of the heme in red blood cells. Wikipedia
Definitions
Relations
Sources
EN
Crigler–Najjar syndrome is a rare inherited disorder affecting the metabolism of bilirubin, a chemical formed from the breakdown of the heme in red blood cells. Wikipedia
Bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase Wikidata
IS A
rare disease
Hereditary hyperbilirubinemia
GENETIC ASSOCIATION
UDP glucuronosyltransferase 1 family, polypeptide A1
HEALTH SPECIALTY
pediatrics
hepatology
NAMED AFTER
Victor Assad Najjar
John Fielding Crigler
Wikipedia
EN
Crigler–Najjar syndrome
Wikidata
EN
Crigler-Najjar syndrome
Wikipedia Redirections
EN
Arias syndrome, Criggler-Najjar Syndrome Type I, Criggler-Najjar Syndrome Type II, Criggler-Najjar Type I, Crigler-Najjar, Crigler-Najjar syndrome, Crigler-Najjar Syndrome, Crigler-najjar syndrome, Crigler-Najjar syndrome, type I, Crigler-Najjar syndrome, type II, Crigler-Najjar Syndrome type 2, Crigler-Najjar syndrome type I, Crigler-Najjar syndrome type II, Crigler najjar, Crigler Najjar disease, Crigler Najjar syndrome, Crigler Najjar syndrome type I, Crigler–Najjar syndrome, type I, Crigler–Najjar syndrome, type II, Crigler–Najjar syndrome type I, Crigler–Najjar syndrome type II, Familial nonhemolytic jaundice
Wikidata Alias
EN
Bilirubin UDP glucuronyl transferase deficiency, Crigler-Najjar syndrome, type I, Crigler Najjar syndrome, Crigler–Najjar syndrome

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