Status: retired, Primitive. Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770533013 | Congenital/hereditary hypermelanotic disorder (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 1781723016 | Congenital/hereditary hypermelanotic disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital/hereditary hypermelanotic disorder | Is a | Disorder of skin | false | Inferred relationship | Some | ||
| Congenital/hereditary hypermelanotic disorder | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
| Congenital/hereditary hypermelanotic disorder | Is a | Congenital disease | false | Inferred relationship | Some | ||
| Congenital/hereditary hypermelanotic disorder | Occurrence | Congenital | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
Description inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set
FHIR