A myelodysplastic/myeloproliferative neoplasm which is characterized by persistent monocytosis, absence of a Philadelphia chromosome and BCR/ABL fusion gene, fewer than 20 percent blasts in the bone marrow and blood, myelodysplasia, and absence of PDGFRA or PDGFRB rearrangement. [ NCIT:C3178 ]
Synonyms: chronic myelomonocytic leukemia (CMML) CMML chronic myelomonocytic leukemia chronic myelomonocytic leukaemia (CMML)
Term information
- GARD:8225 (MONDO:GARD)
- NCIT:C3178 (MONDO:equivalentTo)
- ICDO:9945/3 (NCIT:C3178)
- NANDO:2200014 (https://orcid.org/0000-0003-0011-764X)
- Orphanet:98823 (MONDO:equivalentTo)
- DOID:0080188 (MONDO:equivalentTo)
- ONCOTREE:CMML (MONDO:equivalentTo)
- icd11.foundation:2073226578 (https://orcid.org/0000-0001-5208-3432)
- UMLS:C0023480 (MONDO:equivalentTo)
- EFO:1001779 (MONDO:equivalentTo)
- MedDRA:10009018 (Orphanet:98823/e)
- SCTID:127225006 (MONDO:equivalentTo)
- MEDGEN:44125 (MONDO:equivalentTo)
- MESH:D015477 (Orphanet:98823/e)
gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare
http://purl.obolibrary.org/obo/NCIT_C3178
http://linkedlifedata.com/resource/umls/id/C0023480
http://www.orpha.net/ORDO/Orphanet_98823
http://identifiers.org/mesh/D015477
http://identifiers.org/medgen/44125
http://identifiers.org/snomedct/127225006
http://purl.obolibrary.org/obo/DOID_0080188