Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1771758010 | Inherited disorder of porphyrin metabolism (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1782836013 | Inherited disorder of porphyrin metabolism | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited disorder of porphyrin metabolism (disorder) | est un(e) (attribut) | maladie héréditaire | true | Inferred relationship | Some | ||
| Inherited disorder of porphyrin metabolism (disorder) | est un(e) (attribut) | Disorder of porphyrin metabolism | true | Inferred relationship | Some | ||
| Inherited disorder of porphyrin metabolism (disorder) | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Inherited disorder of porphyrin metabolism (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary sideroblastic anemia | est un(e) (attribut) | False | Inherited disorder of porphyrin metabolism (disorder) | Inferred relationship | Some | |
| Congenital porphyria | est un(e) (attribut) | True | Inherited disorder of porphyrin metabolism (disorder) | Inferred relationship | Some | |
| X-linked sideroblastic anemia with spinocerebellar ataxia | est un(e) (attribut) | False | Inherited disorder of porphyrin metabolism (disorder) | Inferred relationship | Some | |
| X chromosome-linked sideroblastic anemia (disorder) | est un(e) (attribut) | True | Inherited disorder of porphyrin metabolism (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR