Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5143924016 | Hypopigmentation-immunodeficiency disease type 3 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5143925015 | Griscelli syndrome type 3 | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5146508015 | Hypopigmentation-immunodeficiency disease type 3 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Is a | Hypopigmentation-immunodeficiency disease | true | Inferred relationship | Some | ||
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Associated morphology | Decreased melanin pigmentation | true | Inferred relationship | Some | 1 | |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Finding site | Structure of immune system (body structure) | true | Inferred relationship | Some | 2 | |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Finding site | Structure of immune system (body structure) | true | Inferred relationship | Some | 3 | |
| Hypopigmentation-immunodeficiency disease type 3 (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set
FHIR