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 0
Phenotype entries for this disease 0
Associated with 2 genes FLT3, NPM1
Associated tissues -
Disease features -
Remarks -