Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5172589019 | A subtype of myelodysplastic syndrome with atypical features of uncertain clinical significance. The term MDS-U (unclassifiable myelodysplastic syndrome) covers cases that cannot be allocated to another subtype of myelodysplastic syndrome after a full diagnostic work-up has been performed including clinical, morphologic, immunophenotypic or cytogenetic testing. One or more cytopenias are a standard feature of MDS-U but other clinical features are variable. The following cases are considered to fall into this subtype: features of refractory cytopenia with uni or multi-lineage dysplasia but with 1% blasts in peripheral blood, unilineage dysplasia with pancytopenia and persistent cytopenia without morphological features of MDS associated with characteristic cytogenetic abnormalities. The etiology is not known but is thought to involve inherited susceptibility or hematopoietic stem cell damage. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5172590011 | A subtype of myelodysplastic syndrome with atypical features of uncertain clinical significance. The term MDS-U (unclassifiable myelodysplastic syndrome) covers cases that cannot be allocated to another subtype of myelodysplastic syndrome after a full diagnostic work-up has been performed including clinical, morphologic, immunophenotypic or cytogenetic testing. One or more cytopenias are a standard feature of MDS-U but other clinical features are variable. The following cases are considered to fall into this subtype: features of refractory cytopenia with uni or multi-lineage dysplasia but with 1% blasts in peripheral blood, unilineage dysplasia with pancytopenia and persistent cytopenia without morphological features of MDS associated with characteristic cytogenetic abnormalities. The aetiology is not known but is thought to involve inherited susceptibility or haematopoietic stem cell damage. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400475011 | Unclassified myelodysplastic syndrome (MDS-U) is a subtype of myelodysplastic syndrome with atypical features of uncertain clinical significance. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5172586014 | Unclassifiable myelodysplastic syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5172587017 | Unclassifiable myelodysplastic syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5172588010 | MDS-U - unclassifiable myelodysplastic syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Unclassified myelodysplastic syndrome (MDS-U) is a subtype of myelodysplastic syndrome with atypical features of uncertain clinical significance. | Is a | Myelodysplastic syndrome (clinical) | true | Inferred relationship | Some | ||
| Unclassified myelodysplastic syndrome (MDS-U) is a subtype of myelodysplastic syndrome with atypical features of uncertain clinical significance. | Finding site | Bone marrow structure (body structure) | true | Inferred relationship | Some | 1 | |
| Unclassified myelodysplastic syndrome (MDS-U) is a subtype of myelodysplastic syndrome with atypical features of uncertain clinical significance. | Associated morphology | Myelodysplastic neoplasm | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR