Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2006. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
293541015 | Congenital porphyria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
574553012 | Congenital porphyria (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
698661000077115 | porphyrie congénitale (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
76201000077119 | porphyrie congénitale | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital porphyria | est un(e) (attribut) | Disorder of porphyrin metabolism | false | Inferred relationship | Some | ||
Congenital porphyria | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
Congenital porphyria | est un(e) (attribut) | Inherited disorder of porphyrin metabolism (disorder) | true | Inferred relationship | Some | ||
Congenital porphyria | est un(e) (attribut) | Porphyria (disorder) | true | Inferred relationship | Some | ||
Congenital porphyria | est un(e) (attribut) | Disorder of porphyrin and heme metabolism | false | Inferred relationship | Some | ||
Congenital porphyria | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
Congenital porphyria | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Congenital erythropoietic porphyria | est un(e) (attribut) | True | Congenital porphyria | Inferred relationship | Some | |
protoporphyrie érythropoïétique (trouble) | est un(e) (attribut) | True | Congenital porphyria | Inferred relationship | Some | |
Porphobilinogen synthase deficiency | est un(e) (attribut) | True | Congenital porphyria | Inferred relationship | Some |
This concept is not in any reference sets