Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 798214015 | Congenital pigmentary anomaly of skin (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 98624012 | Congenital pigmentary anomaly of skin | 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 pigmentary anomaly of skin (disorder) | est un(e) (attribut) | Skin lesion | false | Inferred relationship | Some | ||
| Congenital pigmentary anomaly of skin (disorder) | est un(e) (attribut) | Congenital anomaly of skin | false | Inferred relationship | Some | ||
| Congenital pigmentary anomaly of skin (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 1 | |
| Congenital pigmentary anomaly of skin (disorder) | morphologie associée (attribut) | Congenital pigmentation | false | Inferred relationship | Some | 1 | |
| Congenital pigmentary anomaly of skin (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital deficiency of pigment of skin | est un(e) (attribut) | False | Congenital pigmentary anomaly of skin (disorder) | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR