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loading...| Preferred Name |
Crigler-Najjar Syndrome [Disease/Finding] |
|
| Synonyms |
Crigler Najjar Syndrome, Type 1 |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000000873 |
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| altLabel |
Crigler Najjar Syndrome, Type 1 Crigler-Najjar Syndrome Hereditary Unconjugated Hyperbilirubinemia Crigler-Najjar Syndrome, Type I Familial Nonhemolytic Unconjugated Hyperbilirubinemia Crigler-Najar Syndrome Crigler Najjar Syndrome |
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| cui |
C0010324 |
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| MESH DEFINITION |
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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| MESH DUI |
D003414 |
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| MeSH name |
Crigler-Najjar Syndrome |
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| MESH UI |
M0005322 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000000873 |
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| NUI |
N0000000873 |
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| prefLabel |
Crigler-Najjar Syndrome [Disease/Finding] |
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| SNOMED CID |
8933000 28259009 |
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| tui |
T047 |
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| subClassOf |
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