acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) Disease Ontology Browser

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Disease Ontology Browser

acute myeloid leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22) (DOID:0081084)
Alliance: disease page
Synonyms: acute myeloid leukemia with abnormal marrow eosinophils; Acute Myeloid Leukemia with inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11
Alt IDs: UMLS_CUI:C0522630
Definition: An acute myeloid leukemia that is characterized by the presence of abnormal bone marrow eosinophils and the characteristic cytogenetic abnormality inv(16)(p13.1q22) or t(16;16)(p13.1;q22), which results in the expression of the fusion protein CBFB-MYH11.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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