|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An acute myeloid leukemia characterized by accumulation of promyelocytes in the bone marrow and by a translocation between chromosomes 15 and 17. (Human Disease Ontology, DOID_0060318)|
|Downloads & Tools|
1 genes associated with the acute promyelocytic leukemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|RARA||retinoic acid receptor, alpha|