Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 94104017 | Congenital hyperpigmentation | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 795116010 | Congenital hyperpigmentation (morphologic abnormality) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4131000052119 | kongenital hyperpigmentering | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| kongenital hyperpigmentering | Is a | medfödd pigmentering | false | Inferred relationship | Some | ||
| kongenital hyperpigmentering | Is a | Hyperpigmentation | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Congenital melanosis of sclera | Associated morphology | False | kongenital hyperpigmentering | Inferred relationship | Some | 2 |
| Congenital melanosis | Associated morphology | False | kongenital hyperpigmentering | Inferred relationship | Some | 2 |
| Neuroectodermal melanolysosomal disease (disorder) | Associated morphology | False | kongenital hyperpigmentering | Inferred relationship | Some | 3 |
| Carney complex (disorder) | Associated morphology | False | kongenital hyperpigmentering | Inferred relationship | Some | 5 |
| Carney complex, trismus, pseudocamptodactyly syndrome | Associated morphology | False | kongenital hyperpigmentering | Inferred relationship | Some | 2 |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR