"Crigler-Najjar Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A familial form of congenital hyperbilirubinemia transmitted as an autosomal recessive trait. It is characterized by icterus and brain damage caused by a glucuronyl transferase deficiency in the liver and faulty bilirubin conjugation.
| Descriptor ID |
D003414
|
| MeSH Number(s) |
C16.320.565.300.281 C18.452.648.300.281
|
| Concept/Terms |
Crigler-Najjar Syndrome- Crigler-Najjar Syndrome
- Crigler Najjar Syndrome, Type 1
- Crigler-Najar Syndrome
- Crigler Najar Syndrome
- Familial Nonhemolytic Unconjugated Hyperbilirubinemia
- Hereditary Unconjugated Hyperbilirubinemia
- Crigler Najjar Syndrome
- Crigler-Najjar Syndrome, Type I
- Crigler Najjar Syndrome, Type I
|
Below are MeSH descriptors whose meaning is more general than "Crigler-Najjar Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Crigler-Najjar Syndrome".
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