acute myelomonocytic leukemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A pediatric acute myeloid leukemia involving both myeloid and monocytoid precursors. At least 20% of non-erythroid cells are of monocytic origin. (Human Phenotype Ontology, HP_0004820)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004820
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Genes

1 genes associated with the acute myelomonocytic leukemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KMT2A lysine (K)-specific methyltransferase 2A