acute myeloid leukemia with mutated RUNX1
Ontology Term:
Status:
Live
Synonym:
Type:
Mapping to OMIM ID:
Comparative Info:
Learn more about this disease from studies in other model systems at the 
WormBase ID:
DOID:0081091
An acute myeloid leukemia that is characterized by de novo RUNX1 gene mutation, not associated with myelodysplastic syndrome-related cytogenetic abnormalities.
Parent:
Child:
Associations based on experimental data:
Disease relevant gene:
Automatic gene association:
1 Inferred automatically: Inferred by orthology to human genes with OMIM annotation
