Crigler-Najjar syndrome
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 (UGT)
Press Enter · cited answer in seconds
0 sources
Summary
Crigler-Najjar syndrome is a rare disease[1]. It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Crigler-Najjar syndrome's instance of is recorded as rare disease[3].
- Crigler-Najjar syndrome's instance of is recorded as class of disease[4].
- John Fielding Crigler is named after Crigler-Najjar syndrome[5].
- Victor Assad Najjar is named after Crigler-Najjar syndrome[6].
- Crigler-Najjar syndrome is a type of bilirubin metabolic disorder[7].
- Crigler-Najjar syndrome is a type of disease[8].
- Crigler-Najjar syndrome's NCI Thesaurus ID is recorded as C84656[9].
- Crigler-Najjar syndrome's health specialty is recorded as pediatrics[10].
- Crigler-Najjar syndrome's health specialty is recorded as hepatology[11].
- Crigler-Najjar syndrome's genetic association is recorded as UGT1A1[12].
- Crigler-Najjar syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3803[13].
- Crigler-Najjar syndrome's exact match is recorded as http://identifiers.org/doid/DOID:3803[14].
- Crigler-Najjar syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
Crigler-Najjar syndrome has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[2] It is known by 25 alternative names across languages and contexts.[16]