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1187123005: Mixed phenotype acute leukemia (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4669995012 Mixed phenotype acute leukemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4669996013 MPAL - mixed phenotype acute leukaemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4669997016 Mixed phenotype acute leukemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4669998014 MPAL - mixed phenotype acute leukemia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4669999018 Mixed phenotype acute leukaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5399566015 A group of rare acute leukemias of ambiguous lineage characterized by the presence of separate populations of blasts of more than one lineage (bilineal), a single population of blasts coexpressing antigens of more than one lineage (biphenotypic), or a combination thereof. The diagnosis relies on immunophenotyping, the T-cell component being characterized by strong expression of cytoplasmic CD3, usually in the absence of surface CD3, the B-cell component expressing CD19, almost always together with CD10, cCD79a, CD22, or PAX5, while the most specific hallmark of the myeloid component is the presence of myeloperoxidase in the blast cytoplasm. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399567012 A group of rare acute leukaemias of ambiguous lineage characterised by the presence of separate populations of blasts of more than one lineage (bilineal), a single population of blasts coexpressing antigens of more than one lineage (biphenotypic), or a combination thereof. The diagnosis relies on immunophenotyping, the T-cell component being characterised by strong expression of cytoplasmic CD3, usually in the absence of surface CD3, the B-cell component expressing CD19, almost always together with CD10, cCD79a, CD22, or PAX5, while the most specific hallmark of the myeloid component is the presence of myeloperoxidase in the blast cytoplasm. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mixed phenotype acute leukemia (disorder) Is a Acute leukemia true Inferred relationship Some
Mixed phenotype acute leukemia (disorder) Finding site Bone marrow structure true Inferred relationship Some 1
Mixed phenotype acute leukemia (disorder) Associated morphology Mixed phenotype acute leukaemia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Acute biphenotypic leukaemia Is a True Mixed phenotype acute leukemia (disorder) Inferred relationship Some
Mixed phenotype acute leukemia with myeloid and B-cell lymphoid phenotypes Is a True Mixed phenotype acute leukemia (disorder) Inferred relationship Some
Mixed phenotype acute leukemia with T-cell and myeloid lineage (disorder) Is a True Mixed phenotype acute leukemia (disorder) Inferred relationship Some
Mixed phenotype acute leukemia with t(9;22) (q34;q11.2); BCR-ABL1 (disorder) Is a True Mixed phenotype acute leukemia (disorder) Inferred relationship Some

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

GB English

US English

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