| Gilbert-syndroom (aandoening) | | Gilbert-syndroom | | syndroom van Gilbert
| | syndroom van Gilbert | | Erfelijke, onschuldige vorm van geelzucht, veroorzaakt door een minder goede werking van bepaalde enzymen in de lever waardoor er een verhoogde concentratie van bilirubine (een afbraakproduct van rode bloedcellen) in het bloed ontstaat. | | Gilbert's syndrome | | Constitutional hepatic dysfunction
Meulengracht syndrome
Gilberts syndrome
Gilbert syndrome
Chronic intermittent juvenile jaundice
Benign unconjugated bilirubinemia syndrome
Gilbert's disease
Congenital familial cholemia
Cholemia familiaris simplex
Familial nonhemolytic jaundice
Gilbert-Lereboullet syndrome
Familial nonhemolytic bilirubinemia
Low-grade chronic hyperbilirubinemia syndrome
Hereditary nonhemolytic jaundice
|
| | Id | 27503000 | | Status | Primitive |
| PALGA thesaurus simple reference set for pathology |
| General Practice / Family Practice reference set |
| International Patient Summary |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E80.4 | | Term | Syndroom van Gilbert |
|
| SNOMED CT to MedDRA simple map | 10018267 |
| SNOMED CT to ICD-10 extended map | | Target | E80.4 | | Rule | TRUE | | Advice | ALWAYS E80.4 | | Correlation | SNOMED CT source code to target map code correlation not specified |
|
|
