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DO Term : acute myeloid leukemia with mutated NPM1 [DOID:0081089] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An acute myeloid leukemia with mutation of the nucleophosmin gene. It is usually associated with normal karyotype and frequently has myelomonocytic or monocytic features.
  • synonyms:
  • ICDO:9877/3,
  • NCI:C82431,
  • SNOMEDCT_US_2023_03_01:703820005,
  • UMLS_CUI:C2826177
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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