Search Ontology:
Human Disease

acute myeloid leukemia with mutated RUNX1

Term ID
DOID:0081091
Synonyms
Definition
An acute myeloid leukemia that is characterized by de novo RUNX1 gene mutation, not associated with myelodysplastic syndrome-related cytogenetic abnormalities. https://pubmed.ncbi.nlm.nih.gov/32871587/
References
  • ICDO:9879/3
  • NCI:C129786
Ontology
Human Disease   ( DOID:0081091 )
Relationships
is a type of
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Genes Involved
Zebrafish Models