Search Ontology:
Human Disease

acute myeloid leukemia with mutated NPM1

Term ID
DOID:0081089
Synonyms
Definition
An acute myeloid leukemia with mutation of the nucleophosmin gene. It is usually associated with normal karyotype and frequently has myelomonocytic or monocytic features. https://pubmed.ncbi.nlm.nih.gov/32609823/
References
  • ICDO:9877/3
  • NCI:C82431
  • SNOMEDCT_US_2023_03_01:703820005
  • UMLS_CUI:C2826177
Ontology
Human Disease   ( DOID:0081089 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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