Mastocytosis - CISMeF

Preferred Label : Mastocytosis;

NCIt synonyms : Mast Cell Disease;

NCIt definition : 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.;

Neoplastic status : Undetermined;

Details

Origin ID

C84269;

UMLS CUI

C0024899;

CISMeF manual mappings
- Mast cell disorder (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Congenital cutaneous mastocytosis [ICD-10 Sub-category]
- Mastocytosis [PASCAL descriptor]
- Mastocytosis [ICD-11 Category]
- Mastocytosis [ICD-10 Sub-category (who)]
- Mastocytosis [HPO term]
- Mastocytosis [MedDRA Preferred Term]
- Mastocytosis [ORDO Disease]
- Mastocytosis [HRDO Sign]
- mastocytosis [DO Concept]
- mastocytosis [Disease (Nov.)]
- mastocytosis [MeSH Descriptor]
- mastocytosis [MeSH concept]
DO Cross reference
- mastocytosis [DO Concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital cutaneous mastocytosis [ICD-10 Sub-category]
- Mast cell activation syndrome [MedDRA Preferred Term]
- Mast cell disorder (disorder) [SNOMED CT concept]
- Mast cell hyperplasia (morphologic abnormality) [SNOMED CT concept]
- Mastocytosis [ORDO Disease]
- Mastocytosis [HPO term]
- Mastocytosis [ICD-10 Sub-category (who)]
- Mastocytosis [MedDRA Preferred Term]
- Mastocytosis (morphologic abnormality) [SNOMED CT concept]
- Mastocytosis, cutaneous [OMIM Phenotype]
- mast cell activation syndrome [Disease (Nov.)]
- mastocytosis [DO Concept]
- mastocytosis [Disease (Nov.)]
- mastocytosis [MeSH concept]
- mastocytosis [MeSH Descriptor]
Validated automatic mappings to NTBT
- Mast Cell Activation Disorders [MeSH Descriptor]
- Mastocytosis, cutaneous [OMIM Phenotype]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Hematopoietic and Lymphoid Cell [NCIt concept]
- Neoplastic Mast Cell [NCIt concept]
- Neoplastic Myeloid Cell [NCIt concept]
disease_has_finding
- Monoclonal Cellular Population Present [NCIt concept]
- Rare Lesion [NCIt concept]
disease_has_normal_cell_origin
- Bone Marrow Stem Cell [NCIt concept]
- Hematopoietic and Lymphoid Cell [NCIt concept]
- Mast Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic Tissue [NCIt concept]
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]

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