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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
    3324918013 Acute myeloid leukemia due to recurrent genetic abnormality (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
    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 Only initial character 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 Only initial character 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
    3392411001000113 Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
    3392411001000113 Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie 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
    Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Is a Acute myeloid leukemia, disease false Inferred relationship Existential restriction modifier (core metadata concept)
    Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Associated morphology Acute myeloid leukemia with recurrent genetic abnormality false Inferred relationship Existential restriction modifier (core metadata concept) 1
    Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Finding site Bone marrow structure false Inferred relationship Existential restriction modifier (core metadata concept) 1

    Inbound Relationships Type Active Source Characteristic Refinability Group
    Acute promyelocytic leukaemia, FAB M3 Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myelomonocytic leukemia - eosinophilic variant Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL (disorder) Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukaemia with t(8;16)(p11;p13) translocation Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukemia with t(6;9)(p23;q34) translocation (disorder) Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukemia with FMS-like tyrosine kinase-3 mutation Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukemia with nucleophosmin 1 somatic mutation (disorder) Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) is a rare subtype of acute myeloid leukemia with recurrent cytogenetic abnormalities characterized by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anemia, thrombocytopenia and nonspecific symptoms related to ineffective hematopoiesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease. Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation (disorder) Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukaemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2); RPN1-EVI1 Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1 (disorder) Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukemia with 11q23 abnormality Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)
    Acute myeloid leukaemia with BCR-ABL1 Is a False Akute myeloblastische Leukämie mit rekurrenter genetischer Anomalie Inferred relationship Existential restriction modifier (core metadata concept)

    Reference Sets

    Concept inactivation indicator attribute value reference set (foundation metadata concept)

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    REPLACED BY association reference set (foundation metadata concept)

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