|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the acute myelomonocytic leukemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|KMT2A||lysine (K)-specific methyltransferase 2A|