Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 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 |
| 770681000241113 | hyperbiliverdinémie (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 887731000172119 | hyperbiliverdinémie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 890941000172112 | jaunisse verte | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 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 | Active | 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 | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperbiliverdinaemia | interprète (attribut) | Pyrrole measurement | true | Inferred relationship | Some | 1 | |
| Hyperbiliverdinaemia | est un(e) (attribut) | Increased biliverdin | true | Inferred relationship | Some | ||
| Hyperbiliverdinaemia | localisation d'une constatation (attribut) | foie | true | Inferred relationship | Some | 2 | |
| Hyperbiliverdinaemia | est un(e) (attribut) | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Hyperbiliverdinaemia | est un(e) (attribut) | affection du foie | true | Inferred relationship | Some | ||
| Hyperbiliverdinaemia | a pour interprétation (attribut) | au-dessus de l'étendue de référence | true | Inferred relationship | Some | 1 | |
| Hyperbiliverdinaemia | est un(e) (attribut) | Digestive system hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR