| Descriptor English: | Crigler-Najjar Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de Crigler-Najjar
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| Descriptor Portuguese: | Síndrome de Crigler-Najjar | ||||||
| Descriptor French: | Syndrome de Crigler-Najjar | ||||||
| Entry term(s): |
Crigler Najar Syndrome Crigler Najjar Syndrome Crigler Najjar Syndrome, Type 1 Crigler-Najar Syndrome Crigler-Najjar Syndrome, Type I Familial Nonhemolytic Unconjugated Hyperbilirubinemia Hereditary Unconjugated Hyperbilirubinemia |
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| Tree number(s): |
C16.320.565.300.281 C18.452.648.300.281 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D003414 | ||||||
| Scope note: | 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 91; was see under HYPERBILIRUBINEMIA, HEREDITARY 1975-90 |
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| Online Note: | use HYPERBILIRUBINEMIA, HEREDITARY to search CRIGLER-NAJJAR SYNDROME 1966-74 |
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| History Note: | 91(75); was see under HYPERBILIRUBINEMIA, HEREDITARY 1975-90 |
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| DeCS ID: | 3432 | ||||||
| Unique ID: | D003414 | ||||||
| NLM Classification: | WD 205.5.H9 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2022/05/23 |
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Crigler-Najjar Syndrome
- Preferred
Crigler Najjar Syndrome, Type 1
- Narrower
| Concept UI |
M0005322 |
| Scope note | 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. |
| Preferred term | Crigler-Najjar Syndrome |
| Entry term(s) |
Crigler Najar Syndrome Crigler Najjar Syndrome Crigler-Najar Syndrome Familial Nonhemolytic Unconjugated Hyperbilirubinemia Hereditary Unconjugated Hyperbilirubinemia |
| Concept UI |
M000756172 |
| Preferred term | Crigler Najjar Syndrome, Type 1 |
| Entry term(s) |
Crigler-Najjar Syndrome, Type I |
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