acute promyelocytic leukemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004836
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
RARA retinoic acid receptor, alpha