Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 412335012 | Ferrochelatase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 412336013 | FECH - Ferrochelatase deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 669159017 | Ferrochelatase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Ferrochelatase deficiency | Is a | Disorder of porphyrin metabolism | true | Inferred relationship | Some | ||
| Ferrochelatase deficiency | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Ferrochelatase deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Ferrochelatase deficiency | Is a | Disorder of porphyrin and haem metabolism | false | Inferred relationship | Some | ||
| Ferrochelatase deficiency | Is a | Enzymopathy | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Erythropoietic protoporphyria due to ferrochelatase deficiency | Due to | True | Ferrochelatase deficiency | Inferred relationship | Some | 1 |
| Erythropoietic protoporphyria | Is a | True | Ferrochelatase deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR