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)

This is just here as a test because I lose it

Term information

database cross reference
  • 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)
Subsets

gard_rare, ordo_disorder, otar, rare, nord_rare, orphanet_rare

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/5507

closeMatch

http://identifiers.org/meddra/10009018

exactMatch

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

id

MONDO:0020311