Search Ontology:
Human Disease

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

Term ID
DOID:0081084
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
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. (2)
References
  • ICDO:9871/3
  • SNOMEDCT_US_2023_03_01:103688009
  • UMLS_CUI:C0522630
Ontology
Human Disease   ( DOID:0081084 )
Relationships
is a type of
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Genes Involved
Zebrafish Models