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loading...| Preferred Name |
Gilbert Disease [Disease/Finding] |
|
| Synonyms |
Hyperbilirubinemia I |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001333 |
|
| altLabel |
Hyperbilirubinemia I Hyperbilirubinemia 1 Unconjugated Benign Bilirubinemia Gilbert Syndrome Gilbert-Lereboullet Syndrome Gilbert's Disease Hyperbilirubinemia, Arias Type Gilbert's Syndrome Meulengracht Syndrome Gilbert Disease Familial Nonhemolytic Jaundice Constitutional Liver Dysfunction |
|
| cui |
C0017551 |
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| MESH DEFINITION |
A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level. |
|
| MESH DUI |
D005878 |
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| MeSH name |
Gilbert Disease |
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| MESH UI |
M0009229 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000001333 |
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| NUI |
N0000001333 |
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| prefLabel |
Gilbert Disease [Disease/Finding] |
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| SNOMED CID |
27503000 |
|
| tui |
T047 |
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| subClassOf |
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