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Disease Ontology Browser
acute myeloid leukemia with mutated NPM1 (DOID:0081089)
Alliance: disease page
Alt IDs: NCI:C82431, UMLS_CUI:C2826177
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory