Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303230012 | Familial progressive hyperpigmentation (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3303231011 | Familial progressive hyperpigmentation | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3303232016 | Melanosis diffusa congenita | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3303233014 | Melanosis universalis hereditaria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3303234015 | Universal melanosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial progressive hyperpigmentation | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Familial progressive hyperpigmentation | Is a | Hereditary disorder of the integument | false | Inferred relationship | Existential restriction modifier | ||
Familial progressive hyperpigmentation | Is a | Hereditary hypermelanosis | true | Inferred relationship | Existential restriction modifier | ||
Familial progressive hyperpigmentation | Associated morphology | Melanosis | true | Inferred relationship | Existential restriction modifier | 1 | |
Familial progressive hyperpigmentation | Finding site | Skin structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Familial progressive hyperpigmentation | Is a | Genetic disorder of skin pigmentation | false | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets