Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3643448014 | Idiopathic CD4 lymphocytopenia (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3643449018 | Idiopathic CD4 lymphocytopenia | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3643450018 | ICL - idiopathic CD4 lymphocytopenia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 766351000241118 | lymphocytopénie CD4 idiopathique (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 984071000172117 | lymphocytopénie CD4 idiopathique | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3657271019 | A rare primary immunodeficiency disorder with characteristics of persistent CD4 T-cell lymphopenia (less than 300 cells/UL on multiple occasions) not associated with any other underlying primary or secondary immune deficiency. Patients typically present opportunistic infections (with cryptococcal, mycobacterial, candidal, varicella zoster virus infections and progressive multifocal leukoencephalopathy being the most prevalent), malignancies (mainly lymphoproliferative disorders), or autoimmune disorders. Some individuals are asymptomatic and incidentally diagnosed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3789572012 | A rare primary immunodeficiency disorder with characteristics of persistent CD4 T-cell lymphopenia (less than 300 cells/UL on multiple occasions) not associated with any other underlying primary or secondary immune deficiency. Patients typically present opportunistic infections (with cryptococcal, mycobacterial, candidal, varicella zoster virus infections and progressive multifocal leucoencephalopathy being the most prevalent), malignancies (mainly lymphoproliferative disorders), or autoimmune disorders. Some individuals are asymptomatic and incidentally diagnosed. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Idiopathic CD4 lymphocytopenia (disorder) | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 3 | |
| Idiopathic CD4 lymphocytopenia (disorder) | Due to | anomalie chromosomique | true | Inferred relationship | Some | 2 | |
| Idiopathic CD4 lymphocytopenia (disorder) | est un(e) (attribut) | maladie idiopathique | true | Inferred relationship | Some | ||
| Idiopathic CD4 lymphocytopenia (disorder) | est un(e) (attribut) | Immunodeficiency associated with chromosomal abnormality | true | Inferred relationship | Some | ||
| Idiopathic CD4 lymphocytopenia (disorder) | est un(e) (attribut) | CD4 T lymphocyte deficiency (disorder) | true | Inferred relationship | Some | ||
| Idiopathic CD4 lymphocytopenia (disorder) | 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