Status: current, Defined. Date: 31-Jan 2006. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 293541015 | Congenital porphyria | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 574553012 | Congenital porphyria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital porphyria | Is a | Disorder of porphyrin metabolism | false | Inferred relationship | Some | ||
| Congenital porphyria | Is a | Congenital disease | true | Inferred relationship | Some | ||
| Congenital porphyria | Is a | Inherited disorder of porphyrin metabolism | true | Inferred relationship | Some | ||
| Congenital porphyria | Is a | Porphyria | true | Inferred relationship | Some | ||
| Congenital porphyria | Is a | Disorder of porphyrin and haem metabolism | false | Inferred relationship | Some | ||
| Congenital porphyria | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Congenital porphyria | Finding site | Body system structure | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital erythropoietic porphyria | Is a | True | Congenital porphyria | Inferred relationship | Some | |
| Erythropoietic protoporphyria | Is a | True | Congenital porphyria | Inferred relationship | Some | |
| 5-aminolevulinic acid dehydratase deficiency | Is a | True | Congenital porphyria | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR