Acute myeloid leukemia with mutated NPM1

Therapeutic area
Hematology
Rare disease
No

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. It usually responds to induction therapy.
Genetic basis
No
Non-human condition
No
Rare disease
No
Listing at source
Listed
Condition name
Acute myeloid leukemia with mutated NPM1
Therapeutic area
Hematology

  • acute myeloid leukemia with mutated NPM1
  • 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

Severity
Severe

  • Hematology
  • Immunology
  • Oncology
  • Rheumatology

MONDO ID
Parent condition
MONDO:0018874

Related records

Broader conditions (32)

Trials (4)

Drugs in development (1)