Status: current. Date: 31-Jan 2019
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3706208012 | A rare genetic hepatic disease characterised by the presence of green colouration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. Can be caused by heterozygous or homozygous mutation in the gene encoding bilirubin reductase-alpha (BLVRA) on chromosome 7p13. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3706209016 | A rare genetic hepatic disease characterized by the presence of green coloration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. Can be caused by heterozygous or homozygous mutation in the gene encoding bilirubin reductase-alpha (BLVRA) on chromosome 7p13. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3706210014 | Hyperbiliverdinaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3706211013 | Hyperbiliverdinemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3706212018 | Hyperbiliverdinemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5405112013 | Hyperbiliverdinemia is a rare, genetic hepatic disease characterized by the presence of green coloration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5405113015 | Hyperbiliverdinaemia is a rare, genetic hepatic disease characterised by the presence of green colouration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperbiliverdinaemia | Is a | Biliverdin above reference range | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Hyperbiliverdinaemia | Is a | Autosomal hereditary disorder | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Hyperbiliverdinaemia | Is a | Disease of liver | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Hyperbiliverdinaemia | Has interpretation | Above reference range | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Hyperbiliverdinaemia | Interprets | Pyrrole measurement | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Hyperbiliverdinaemia | Finding site | Liver structure | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR