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 |
2477785019 | Deficiency of argininosuccinate lyase | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
68418017 | Argininosuccinate lyase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
68419013 | Argininosuccinic aciduria | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
68420019 | ASAL deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
68421015 | ASL deficiency | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
777754012 | Argininosuccinate lyase 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 |
Argininosuccinate lyase deficiency | est un(e) (attribut) | Enzymopathy | false | Inferred relationship | Some | ||
Argininosuccinate lyase deficiency | est un(e) (attribut) | Disorder of the urea cycle metabolism | true | Inferred relationship | Some | ||
Argininosuccinate lyase deficiency | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Argininosuccinate lyase deficiency | est un(e) (attribut) | Specific enzyme deficiency | true | Inferred relationship | Some | ||
Argininosuccinate lyase deficiency | est un(e) (attribut) | Inborn error of metabolism | true | Inferred relationship | Some | ||
Argininosuccinate lyase deficiency | localisation d'une constatation (attribut) | structure d'un système corporel | false | Inferred relationship | Some | ||
Argininosuccinate lyase deficiency | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets