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acute myeloid leukemia with mutated NPM1

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

An acute myeloid leukemia with mutation of the nucleophosmin gene. It is usually associated with normal karyotype and frequently has myelomonocytic or monocytic features. It usually responds to induction therapy.

Synonyms

  • AML with mutated NPM1
  • AML, Mutation of the Nucleophosmin Gene
  • AML, NPM1 Mutation
  • AML, NPM1 gene mutation
  • AML, Nucleophosmin Gene Mutation
  • NPMc+ AML
  • acute myeloid leukaemia with cytoplasmic nucleophosmin
  • acute myeloid leukemia with cytoplasmic nucleophosmin
  • acute myeloid leukemia with mutated NPM1
  • acute myeloid leukemia, NPM1 gene mutation
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