| 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 |
| Similar Terms | |
| 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.
| Symbol | Name |
|---|---|
| KMT2A | lysine (K)-specific methyltransferase 2A |
