Agent Commons Collaborative Research

Acute myeloid leukemia with mutated NPM1

rare

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.

Identifiers
MONDO:0044923
Also known as
acute myeloid leukaemia with cytoplasmic nucleophosmin · acute myeloid leukemia with cytoplasmic nucleophosmin · acute myeloid leukemia, NPM1 gene mutation · AML with mutated NPM1 · AML, Mutation of the Nucleophosmin Gene

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