Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770730013 | Congenital/hereditary lentiginosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1781898014 | Congenital/hereditary lentiginosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1857221000052114 | medfödd eller ärftlig lentiginos | 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 |
| medfödd eller ärftlig lentiginos | Is a | Lentiginosis (disorder) | false | Inferred relationship | Some | ||
| medfödd eller ärftlig lentiginos | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
| medfödd eller ärftlig lentiginos | Is a | Congenital disease (disorder) | false | Inferred relationship | Some | ||
| medfödd eller ärftlig lentiginos | Associated morphology | Pigment deposition | false | Inferred relationship | Some | 1 | |
| medfödd eller ärftlig lentiginos | Occurrence | Congenital | false | Inferred relationship | Some | ||
| medfödd eller ärftlig lentiginos | Associated morphology | ökad melaninpigmentering | false | Inferred relationship | Some | 1 | |
| medfödd eller ärftlig lentiginos | Associated morphology | ökad melaninpigmentering | false | Inferred relationship | Some | 1 | |
| medfödd eller ärftlig lentiginos | Finding site | Skin structure | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| ärftlig lentiginos | Is a | False | medfödd eller ärftlig lentiginos | Inferred relationship | Some | |
| Nevoid lentiginosis (disorder) | Is a | False | medfödd eller ärftlig lentiginos | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR