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
- UMLS:C0024899 (MONDO:equivalentTo)
- NCIT:C84269 (MONDO:equivalentTo)
- MedDRA:10026891 (Orphanet:98292/e)
- GARD:6987 (MONDO:GARD)
- MESH:D008415 (Orphanet:98292/e)
- MEDGEN:9902 (MONDO:equivalentTo)
- NORD:1408 (MONDO:NORD)
- EFO:0009001 (MONDO:equivalentTo)
- icd11.foundation:691643472 (Orphanet:98292)
- Orphanet:98292 (OMIM:154800)
- ICD10WHO:Q82.2 (MONDO:equivalentTo)
- DOID:350 (MONDO:equivalentTo)
- ONCOTREE:MCD (MONDO:equivalentTo)
gard_rare, matrix_llm__is_cancer_other, matrix_txgnn_grouping_cancer_or_benign_tumor, disease_grouping, mondo_top_grouping_member, matrix_llm__txgnn_other, harrisons_view_immune_system_disorder, matrix_included, nord_rare, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, mondo_top_grouping_immune_system_disorder, rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_hematologic_disorder, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_hematologic_disorder, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, harrisons_view_hereditary_disease, ordo_group_of_disorders
http://www.ebi.ac.uk/efo/EFO_0009001
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://purl.obolibrary.org/obo/mondo/sources/icd11foundation/691643472
http://identifiers.org/mesh/D008415
https://icd.who.int/browse10/2019/en#/Q82.2