Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 351575018 | Deletion of X-chromosome and hypogammaglobulinemia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 351576017 | Deletion of X-chromosome and hypogammaglobulinaemia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 622984017 | Deletion of X-chromosome and hypogammaglobulinemia (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Deletion of X-chromosome and hypogammaglobulinemia | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 3 | |
| Deletion of X-chromosome and hypogammaglobulinemia | est un(e) (attribut) | Disorder of immune structure (disorder) | true | Inferred relationship | Some | ||
| Deletion of X-chromosome and hypogammaglobulinemia | associé à (attribut) | anomalie chromosomique | true | Inferred relationship | Some | 2 | |
| Deletion of X-chromosome and hypogammaglobulinemia | est défini par la manifestation de (attribut) | Immune system finding | false | Inferred relationship | Some | ||
| Deletion of X-chromosome and hypogammaglobulinemia | est un(e) (attribut) | Immunodeficiency associated with chromosomal abnormality | true | Inferred relationship | Some | ||
| Deletion of X-chromosome and hypogammaglobulinemia | localisation d'une constatation (attribut) | structure du système immunitaire | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR