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 |
| 1005621000172119 | hyperlymphocytose B polyclonale persistante | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3644793014 | Persistent polyclonal B-cell lymphocytosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3644795019 | Persistent polyclonal B-cell lymphocytosis (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3644797010 | Persistent polyclonal B-cell lymphocytosis with binucleated lymphocytes | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3644798017 | PPBL - persistent polyclonal B-cell lymphocytosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 766671000241119 | lymphocytose B polyclonale persistante (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 887211000172115 | lymphocytose B polyclonale persistante | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3644794015 | A rare generally benign lymphoproliferative hematological disease characterized by chronic, stable, persistent, polyclonal lymphocytosis of memory B-cell origin, the presence of binucleated lymphocytes in the peripheral blood, and a polyclonal increase in serum immunoglobulin M (IgM). Patients are most frequently asymptomatic or may present with mild splenomegaly. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3644796018 | A rare generally benign lymphoproliferative haematological disease characterised by chronic, stable, persistent, polyclonal lymphocytosis of memory B-cell origin, the presence of binucleated lymphocytes in the peripheral blood, and a polyclonal increase in serum immunoglobulin M (IgM). Patients are most frequently asymptomatic or may present with mild splenomegaly. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Persistent polyclonal B-cell lymphocytosis | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 3 | |
| Persistent polyclonal B-cell lymphocytosis | morphologie associée (attribut) | Lymphoproliferative disorder (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
| Persistent polyclonal B-cell lymphocytosis | est un(e) (attribut) | Persistent lymphocytosis | true | Inferred relationship | Some | ||
| Persistent polyclonal B-cell lymphocytosis | est un(e) (attribut) | trouble lymphoprolifératif | true | Inferred relationship | Some | ||
| Persistent polyclonal B-cell lymphocytosis | interprète (attribut) | Lymphocyte count | true | Inferred relationship | Some | 1 | |
| Persistent polyclonal B-cell lymphocytosis | a pour interprétation (attribut) | au-dessus de l'étendue de référence | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR