obsolete_acute promyelocytic leukemia true APL acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants acute promyelocytic leukemia acute promyelocytic leukemia with t(15;17)(q22;q12); PML-rara APML ICD10:C92.40 ICDO:9866/3 acute myeloblastic leukemia type 3 AML with t(15;17)(q22;q12) acute myeloid leukemia M3 OMIM:612376 GARD:0000538 ICD10:C92.4 MedDRA:10001019 DOID:0060318 APML - acute promyelocytic leukemia 3.88.0 Orphanet:520 acute promyelocytic leukemia with PML-rara acute promyelocytic leukemia with t(15;17)(q22;q12); PML/rara acute myeloblastic leukemia 3 leukemia, acute promyelocytic promyelocytic leukemia Replaced by Mondo term MONDO_0012883, with which this term was previously merged. Use: http://purl.obolibrary.org/obo/MONDO_0012883 SCTID:110004001 http://purl.obolibrary.org/obo/MONDO_0012883 NCIT:C3182 EFO:0000224 MESH:D015473 Acute promyelocytic leukemia (APL) is an aggressive form of acute myeloid leukemia (AML), characterized by arrest of leukocyte differentiation at the promyelocyte stage, due to a specific chromosomal translocation t(15;17) in myeloid cells. APL manifests with easy bruising, hemorrhagic diathesis and fatigue. AML M3 FAB M3 UMLS:C0023487 AML with t(15;17)(q22;q12);(PML/RARalpha) and variants