| Descriptor English: | Gilbert Disease | ||||
| Descriptor Spanish: |
Enfermedad de Gilbert
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| Descriptor Portuguese: | Doença de Gilbert | ||||
| Descriptor French: | Maladie de Gilbert | ||||
| Entry term(s): |
Arias Type Hyperbilirubinemia Arias Type Hyperbilirubinemias Constitutional Liver Dysfunction Disease, Gilbert Disease, Gilbert's Familial Nonhemolytic Jaundice Gilbert Syndrome Gilbert's Disease Gilbert's Syndrome Gilbert-Lereboullet Syndrome Gilberts Disease Gilberts Syndrome Hyperbilirubinemia 1 Hyperbilirubinemia 1s Hyperbilirubinemia I Hyperbilirubinemia, Arias Type Hyperbilirubinemias, Arias Type Meulengracht Syndrome Syndrome, Gilbert Syndrome, Gilbert's Unconjugated Benign Bilirubinemia |
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| Tree number(s): |
C16.320.565.300.528 C18.452.648.300.528 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D005878 | ||||
| Scope note: | 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. |
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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: | 2000; see GILBERT'S DISEASE 1991-1999, see HYPERBILIRUBINEMIA, HEREDITARY 1975-90 |
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| History Note: | 2000(1975) |
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| Entry Version: | GILBERT DIS |
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| DeCS ID: | 6017 | ||||
| Unique ID: | D005878 | ||||
| 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: | 2013/07/08 |
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Gilbert Disease
- Preferred
| Concept UI |
M0009229 |
| Scope note | 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. |
| Preferred term | Gilbert Disease |
| Entry term(s) |
Arias Type Hyperbilirubinemia Arias Type Hyperbilirubinemias Constitutional Liver Dysfunction Disease, Gilbert Disease, Gilbert's Familial Nonhemolytic Jaundice Gilbert Syndrome Gilbert's Disease Gilbert's Syndrome Gilbert-Lereboullet Syndrome Gilberts Disease Gilberts Syndrome Hyperbilirubinemia 1 Hyperbilirubinemia 1s Hyperbilirubinemia I Hyperbilirubinemia, Arias Type Hyperbilirubinemias, Arias Type Meulengracht Syndrome Syndrome, Gilbert Syndrome, Gilbert's Unconjugated Benign Bilirubinemia |
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