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415285009: Myelodysplastic syndrome with multilineage dysplasia (disorder)


    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
    2534454017 Refractory cytopenia with multilineage dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    2534455016 Refractory cytopaenia with multilineage dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4953726015 Myelodysplastic syndrome with multilineage dysplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4953727012 Myelodysplastic syndrome with multilineage dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    880361000172113 cytopénie réfractaire avec dysplasie multilignée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    1101301000241115 syndrome myélodysplasique avec dysplasie multilignée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    3424731001000119 Zytopenie, refraktäre mit multilineärer Dysplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    syndrome myélodysplasique avec dysplasie multilignée Is a Myelodysplastic syndrome (clinical) false Inferred relationship Some
    syndrome myélodysplasique avec dysplasie multilignée Is a Primary malignant neoplasm of bone marrow false Inferred relationship Some
    syndrome myélodysplasique avec dysplasie multilignée Finding site Bone marrow structure false Inferred relationship Some 1
    syndrome myélodysplasique avec dysplasie multilignée Associated morphology Myelodysplastic syndrome with multilineage dysplasia false Inferred relationship Some 1
    syndrome myélodysplasique avec dysplasie multilignée Associated morphology Myelodysplastic syndrome with multilineage dysplasia false Inferred relationship Some 1
    syndrome myélodysplasique avec dysplasie multilignée Finding site Bone marrow structure false Inferred relationship Some 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    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. Is a False syndrome myélodysplasique avec dysplasie multilignée Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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