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1264416003: Unclassifiable myelodysplastic syndrome (disorder)


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
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
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 Active 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 Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Unclassifiable myelodysplastic syndrome (disorder) Is a Myelodysplastic syndrome (clinical) true Inferred relationship Some
Unclassifiable myelodysplastic syndrome (disorder) Finding site Bone marrow structure true Inferred relationship Some 1
Unclassifiable myelodysplastic syndrome (disorder) Associated morphology Myelodysplastic neoplasm true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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