Disease #00162 (AML (Acute myeloid leukemia), OMIM:601626)

Official abbreviation AML
Name Acute myeloid leukemia
OMIM ID 601626
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Somatic mutation
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 2 genes FLT3, NPM1
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Disease features -
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