Status: current, Primitive. 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 | Case insensitive | SNOMED CT core |
| 1782836013 | Inherited disorder of porphyrin metabolism | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Inherited disorder of porphyrin metabolism | Is a | Hereditary disease | false | Inferred relationship | Some | ||
| Inherited disorder of porphyrin metabolism | Is a | Hereditary metabolic disease | true | Inferred relationship | Some | ||
| Inherited disorder of porphyrin metabolism | Is a | Disorder of porphyrin metabolism | true | Inferred relationship | Some | ||
| Inherited disorder of porphyrin metabolism | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Inherited disorder of porphyrin metabolism | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary sideroblastic anaemia | Is a | False | Inherited disorder of porphyrin metabolism | Inferred relationship | Some | |
| Congenital porphyria | Is a | True | Inherited disorder of porphyrin metabolism | Inferred relationship | Some | |
| X-linked sideroblastic anaemia with spinocerebellar ataxia | Is a | False | Inherited disorder of porphyrin metabolism | Inferred relationship | Some | |
| X chromosome-linked sideroblastic anaemia | Is a | True | Inherited disorder of porphyrin metabolism | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR