Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2465507011 | Tyrosinemia type I (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2469188016 | Tyrosinaemia type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2469662018 | Tyrosinemia type I | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 846041000052111 | tyrosinemi, typ 1 | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Tyrosinemia type I (disorder) | Is a | Clinical manifestation of enzyme deficiency (disorder) | true | Inferred relationship | Some | ||
| Tyrosinemia type I (disorder) | Is a | Hereditary hypertyrosinemia | true | Inferred relationship | Some | ||
| Tyrosinemia type I (disorder) | Due to | Deficiency of fumarylacetoacetase | true | Inferred relationship | Some | 1 | |
| Tyrosinemia type I (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Tyrosinemia type I (disorder) | Is a | Hereditary cancer-predisposing syndrome | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR