A clonal myeloproliferative neoplasm characterized by the proliferation and accumulation of neoplastic mast cells in one or multiple organs or organ systems. It is a heterogeneous group of neoplasms, ranging from cutaneous proliferations which may regress spontaneously, to aggressive neoplasms associated with organ failure and short survival. [ NCIT:C84269 ]
Synonyms: Mast cell disease mastocytosis mast cell hyperplasia
Term information
- NCIT:C84269 (MONDO:equivalentTo)
- icd11.foundation:691643472 (Orphanet:98292)
- UMLS:C0024899 (MONDO:equivalentTo)
- Orphanet:98292 (OMIM:154800)
- DOID:350 (MONDO:equivalentTo)
- ICD10WHO:Q82.2 (MONDO:equivalentTo)
- MEDGEN:9902 (MONDO:equivalentTo)
- ONCOTREE:MCD (MONDO:equivalentTo)
- EFO:0009001 (MONDO:equivalentTo)
- MedDRA:10026891 (Orphanet:98292/e)
- NORD:1408 (MONDO:NORD)
- MESH:D008415 (Orphanet:98292/e)
- GARD:6987 (MONDO:GARD)
gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders
http://purl.obolibrary.org/obo/DOID_350
http://www.orpha.net/ORDO/Orphanet_98292
http://identifiers.org/medgen/9902
http://purl.obolibrary.org/obo/NCIT_C84269
http://linkedlifedata.com/resource/umls/id/C0024899
http://identifiers.org/mesh/D008415
https://icd.who.int/browse10/2019/en#/Q82.2