"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.
- 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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