Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770707019 | Congenital/hereditary cutis laxa (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1781877014 | Congenital/hereditary cutis laxa | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital/hereditary cutis laxa (disorder) | est un(e) (attribut) | cutis laxa | false | Inferred relationship | Some | ||
| Congenital/hereditary cutis laxa (disorder) | localisation d'une constatation (attribut) | Connective tissue structure | false | Inferred relationship | Some | ||
| Congenital/hereditary cutis laxa (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | ||
| Congenital/hereditary cutis laxa (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Congenital/hereditary cutis laxa (disorder) | est un(e) (attribut) | affection congénitale du tissu conjonctif | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Cutis laxa secondary to inherited disorder of connective tissue (disorder) | est un(e) (attribut) | False | Congenital/hereditary cutis laxa (disorder) | Inferred relationship | Some | |
| SCARF syndrome | est un(e) (attribut) | False | Congenital/hereditary cutis laxa (disorder) | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR