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128836009: Myelodysplastic syndrome with multilineage dysplasia (morphologic abnormality)

    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2023. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    207429012 Refractory cytopenia with multilineage dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3009266015 Refractory cytopenia of childhood en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4953715014 Myelodysplastic syndrome with multilineage dysplasia (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4953716010 Myelodysplastic syndrome with multilineage dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

    0 descendants.

    Expanded Value Set

    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Myelodysplastic syndrome with multilineage dysplasia Is a Malignant neoplasm, primary false Inferred relationship Some
    Myelodysplastic syndrome with multilineage dysplasia Is a Myelodysplastic syndrome false Inferred relationship Some
    Myelodysplastic syndrome with multilineage dysplasia Is a Myelodysplastic neoplasm false Inferred relationship Some
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Refractory cytopenia with multilineage dysplasia and ringed sideroblasts Is a False Myelodysplastic syndrome with multilineage dysplasia Inferred relationship Some
    syndrome myélodysplasique avec dysplasie multilignée Associated morphology False Myelodysplastic syndrome with multilineage dysplasia Inferred relationship Some 1
    syndrome myélodysplasique avec dysplasie multilignée Associated morphology False Myelodysplastic syndrome with multilineage dysplasia Inferred relationship Some 1
    A rare multiple congenital anomalies/dysmorphic syndrome characterized by early-onset progressive bone marrow failure with anemia, leukopenia, mild thrombopenia, and myelodysplastic features, as well as non-hematologic manifestations, such as developmental delay, cataracts, facial dysmorphism, short stature, and skeletal anomalies. Immunodeficiency primarily affects B-cells and may lead to increased susceptibility to infections. Additional reported features include dry skin and eczema, cardiac anomalies, hearing loss, and reduction of cerebral volume on brain imaging. Associated morphology False Myelodysplastic syndrome with multilineage dysplasia Inferred relationship Some 1

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    REPLACED BY association reference set (foundation metadata concept)

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