Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial progressive hyperpigmentation (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Familial progressive hyperpigmentation (disorder) | est un(e) (attribut) | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Familial progressive hyperpigmentation (disorder) | est un(e) (attribut) | Hereditary hypermelanosis (disorder) | true | Inferred relationship | Some | ||
Familial progressive hyperpigmentation (disorder) | morphologie associée (attribut) | mélanose (anomalie morphologique) | true | Inferred relationship | Some | 1 | |
Familial progressive hyperpigmentation (disorder) | localisation d'une constatation (attribut) | structure de la peau | true | Inferred relationship | Some | 1 | |
Familial progressive hyperpigmentation (disorder) | est un(e) (attribut) | Genetic disorder of skin pigmentation (disorder) | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets