Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303230012 | Familial progressive hyperpigmentation (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3303231011 | Familial progressive hyperpigmentation | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303232016 | Melanosis diffusa congenita | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303233014 | Melanosis universalis hereditaria | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303234015 | Universal melanosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303235019 | Patches of hyperpigmentation in the skin, which are present at birth or in early infancy and increase in size and number with age. A rare autosomal dominant disorder. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial progressive hyperpigmentation | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Familial progressive hyperpigmentation | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Familial progressive hyperpigmentation | Is a | Hereditary hypermelanosis | true | Inferred relationship | Some | ||
Familial progressive hyperpigmentation | Associated morphology | Melanosis | true | Inferred relationship | Some | 1 | |
Familial progressive hyperpigmentation | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Familial progressive hyperpigmentation | Is a | Genetic disorder of skin pigmentation | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set