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721305008: Acute myeloid leukemia due to recurrent genetic abnormality (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
    3324918013 Acute myeloid leukemia due to recurrent genetic abnormality (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3324919017 Acute myeloid leukemia due to recurrent genetic abnormality en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3324920011 Acute myeloid leukaemia due to recurrent genetic abnormality 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
    Acute myeloid leukemia due to recurrent genetic abnormality Is a Acute myeloid leukemia, disease false Inferred relationship Some
    Acute myeloid leukemia due to recurrent genetic abnormality Associated morphology Acute myeloid leukemia with recurrent genetic abnormality false Inferred relationship Some 1
    Acute myeloid leukemia due to recurrent genetic abnormality Finding site Bone marrow structure false Inferred relationship Some 1
    Inbound Relationships Type Active Source Characteristic Refinability Group
    Acute promyelocytic leukaemia, FAB M3 Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myelomonocytic leukemia - eosinophilic variant Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL (disorder) Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with t(8;16)(p11;p13) translocation (disorder) Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with t(6;9)(p23;q34) translocation (disorder) Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukaemia with CEBPA somatic mutations Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with 11q23 abnormality (disorder) Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some
    Acute myeloid leukemia with BCR-ABL1 Is a False Acute myeloid leukemia due to recurrent genetic abnormality Inferred relationship Some

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    REPLACED BY association reference set (foundation metadata concept)

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