loading...| Preferred Name |
Gilbert Disease |
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| Synonyms |
|
|
| Definitions |
A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity. |
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| ID |
http://www.phoc.org.cn/pmo/class/PMO_00036679 |
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| Database_Cross_Reference |
CSP:1654-1020 CHV:0000005493 CCPSS:0055962 MTH:NOCODE NCI:C84729 MEDCIN:30164 MEDCIN:273601 ICD10:E80.4 DXP:U000711 ICPC2P:T99013 SNM:D-1503 ICD10AM:E80.4 DO:DOID:2739 COSTAR:U000325 MEDLINEPLUS:310 SNOMEDCT_US:27503000 MSH:D005878 NDFRT:N0000001333 SNOMEDCT_US:267509000 OMIM:191740 SNM:D-1501 ICD10CM:E80.4 OMIM:MTHU031877 SNOMEDCT_US:154770008 OMIM:143500 DXP:NOCODE SNMI:D6-85100 MDR:10018267 RCD:C3742 MTHICD9:277.4 |
|
| Definition |
A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity. |
|
| label |
Gilbert Disease |
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| MCID |
MC00005602 |
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| PMOID |
PMO:00036679 |
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| prefixIRI |
pmo:PMO_00036679 |
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| prefLabel |
Gilbert Disease |
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| Synonym |
HYPERBILIRUBINEMIA, GILBERT TYPE Gilberts Disease Disease, Gilbert's Gilbert's Disease Familial nonhemolytic bilirubinemia Syndrome, Gilbert's Constitutional hyperbilirubinemia HYPERBILIRUBINEMIA, ARIAS TYPE HBLRG Hereditary nonhaemolytic jaundice GILBERT'S DISEASE Gilbert-Lereboullet syndrome gilbert's disease Gilbert-Meulengracht syndrome Cholaemia familiaris simplex Constitutional hepatic dysfunction syndrome Gilberts disease Familial nonhaemolytic bilirubinaemia Gilbert syndrome Disease, Gilbert Hyperbilirubinemia, constitutional gilbert syndrome familial nonhemolytic jaundice syndrome gilbert's Hyperbilirubinemia, unconjugated, chronic non-hemolytic Syndrome, Gilbert Benign unconjugated bilirubinaemia syndrome GILBERT-LEREBOULLET SYNDROME Benign unconjugated bilirubinemia syndrome Gilbert's disease Congenital familial cholemia GILBERT DISEASE Gilbert-Lereboullet Syndrome GILBERT DIS GILBERTS DIS Jaundice, congenital nonhemolytic Hyperbilirubinemias, Arias Type Familial non-hemolytic jaundice Hyperbilirubinemia, Arias Type Hyperbilirubinemia 1 Meulengracht Syndrome GILBERT SYNDROME Gilbert's syndrome Constitutional Liver Dysfunction Gilbert Disease (disorder) Disease;Gilberts HYPERBILIRUBINEMIA, FAMILIAL UNCONJUGATED HYPERBILIRUBINEMIA, CHRONIC UNCONJUGATED Low-grade chronic hyperbilirubinaemia syndrome Unconjugated Benign Bilirubinemia Meulengracht syndrome Gilberts syndrome gilbert's syndrome Familial nonhaemolytic jaundice Gilbert Syndrome Gilbert's Syndrome Congenital familial cholaemia Constitutional hepatic dysfunction HYPERBILIRUBINEMIA I gilberts syndrome Hyperbilirubinemia 1s constitutional hyperbilirubinemia Arias Type Hyperbilirubinemias gilbert syndromes gilberts disease Hyperbilirubinemia I Arias Type Hyperbilirubinemia Familial Nonhemolytic Jaundice Gilbert's syndrome (diagnosis) hereditary nonhemolytic jaundice Gilbert Disease [Disease/Finding] congenital nonhemolytic jaundice diseases gilbert Familial nonhemolytic jaundice Chronic intermittent juvenile jaundice constitutional hyperbilirubinemia (diagnosis) meulengracht syndrome Hereditary nonhemolytic jaundice gilbert disease Gilbert's syndrome (disorder) Low-grade chronic hyperbilirubinemia syndrome Gilberts Syndrome Cholemia familiaris simplex |
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| Tree Number |
T9.8.4.14.9.3 T9.11.1.12.9.3 |
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| subClassOf |