Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 412330019 | Porphobilinogen deaminase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 412331015 | PBGD - Porphobilinogen deaminase deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 412332010 | Uroporphyrinogen 1 synthase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 412333017 | PBGD deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 669157015 | Porphobilinogen deaminase deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Porphobilinogen deaminase deficiency | est un(e) (attribut) | Disorder of porphyrin metabolism | true | Inferred relationship | Some | ||
| Porphobilinogen deaminase deficiency | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
| Porphobilinogen deaminase deficiency | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Porphobilinogen deaminase deficiency | est un(e) (attribut) | Disorder of porphyrin and heme metabolism | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acute intermittent porphyria | est un(e) (attribut) | True | Porphobilinogen deaminase deficiency | Inferred relationship | Some |
This concept is not in any reference sets
FHIR