acute myeloid leukemia with minimal differentiation
Go to external page http://purl.obolibrary.org/obo/MONDO_0005223
An acute myeloid leukemia (AML) in which the blasts do not show evidence of myeloid differentiation by morphology and conventional cytochemistry. (WHO, 2001) [ NCIT:C8460 ]
Synonyms: acute myeloblastic leukemia, minimally differentiated minimally differentiated acute myeloblastic leukaemia AML M0 acute myelogenous leukemia with minimal differentiation acute myeloid leukemia with minimal differentiation minimally differentiated acute myeloblastic leukemia M0 acute myelogenous leukemia with minimal differentiation acute myelogenous leukaemia with minimal differentiation acute myelocytic leukemia with minimal differentiation acute myelocytic leukaemia with minimal differentiation M0 myeloid leukemia with minimal differentiation acute myeloid leukaemia with minimal differentiation (MO) M0 acute myeloblastic leukemia acute myeloid leukemia with minimal differentiation (MO) AML with minimal differentiation acute myeloblastic leukemia with minimal differentiation M0 acute myeloblastic leukaemia M0 acute myelocytic leukaemia M0 acute granulocytic leukaemia with minimal differentiation M0 acute granulocytic leukaemia M0 myeloid leukaemia M0 acute granulocytic leukemia M0 acute myelocytic leukemia M0 acute myelogenous leukaemia with minimal differentiation M0 myeloid leukaemia with minimal differentiation M0 acute myelogenous leukemia M0 acute granulocytic leukemia with minimal differentiation acute myeloid leukemia, minimally differentiated M0 myeloid leukemia acute myeloblastic leukaemia with minimal differentiation M0 acute myelogenous leukaemia
Term information
- DOID:0081085 (MONDO:equivalentTo)
- NANDO:2200004 (https://orcid.org/0000-0003-0011-764X)
- UMLS:C0522631 (MONDO:equivalentTo)
- icd11.foundation:1468530237 (https://orcid.org/0000-0001-5208-3432)
- MEDGEN:101100 (MONDO:equivalentTo)
- NCIT:C8460 (MONDO:equivalentTo)
- ONCOTREE:AMLMD (MONDO:equivalentTo)
- Orphanet:98832 (MONDO:equivalentTo)
- GARD:19588 (MONDO:GARD)
- EFO:0003026 (MONDO:equivalentTo)
- ICDO:9872/3 (NCIT:C8460)
ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare
http://identifiers.org/medgen/101100
http://purl.obolibrary.org/obo/NCIT_C8460
http://linkedlifedata.com/resource/umls/id/C0522631
http://purl.obolibrary.org/obo/DOID_0081085
http://www.orpha.net/ORDO/Orphanet_98832