Indolent Systemic Mastocytosis

Preferred Label : Indolent Systemic Mastocytosis;

NCIt synonyms : ISM;

NCIt definition : An indolent mast cell neoplasm characterized by systemic infiltration of skin and internal organs by aggregates of neoplastic mast cells. There is no evidence of mast cell leukemia or clonal hematologic malignancy. Clinically, there is no evidence of palpable hepatomegaly and splenomegaly, malabsorption syndrome, or pathologic fractures.;

Neoplastic status : Undetermined;

ICD-O code : 9741/1;

Details

Origin ID

C9286;

UMLS CUI

C0272203;

Currated CISMeF NLP mapping
- Indolent systemic mastocytosis [ORDO Disease]
- Indolent systemic mastocytosis [MedDRA LLT]
- Indolent systemic mastocytosis (disorder) [SNOMED CT concept]
- Indolent systemic mastocytosis (morphologic abnormality) [SNOMED CT concept]
- indolent systemic mastocytosis [MeSH concept]
- indolent systemic mastocytosis [SNOMED Notion]
DO Cross reference
- indolent systemic mastocytosis [DO Concept]
Disease may have findings
- Cutaneous Involvement [NCIt concept]
- Serum Total Tryptase Levels Increased [NCIt concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Indolent systemic mastocytosis [ORDO Disease]
- Indolent systemic mastocytosis [MedDRA LLT]
- Indolent systemic mastocytosis [MedDRA Preferred Term]
- Indolent systemic mastocytosis (disorder) [SNOMED CT concept]
- Indolent systemic mastocytosis (morphologic abnormality) [SNOMED CT concept]
- indolent systemic mastocytosis [DO Concept]
- indolent systemic mastocytosis [SNOMED Notion]
- indolent systemic mastocytosis [MeSH concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology Terminology [NCIt concept]
- Mapped ICDO3.1 Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
disease_excludes_finding
- Cytopenia [NCIt concept]
- Hepatomegaly [NCIt concept]
- Hypersplenism [NCIt concept]
- Lytic Bone Lesion [NCIt concept]
- Malabsorption Syndrome [NCIt concept]
- Pathologic Fracture [NCIt concept]
- Portal Hypertension [NCIt concept]
- Splenomegaly [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
- Indolent Clinical Course [NCIt concept]
- Monoclonal Cellular Population Present [NCIt concept]
- Primary Lesion [NCIt concept]
- Rare Lesion [NCIt concept]
- Systemic Disease [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]
disease_mapped_to_gene
- KIT Gene [NCIt concept]
disease_may_have_molecular_abnormality
- C-KIT Somatic Point Mutation [NCIt concept]
- C-KIT Tyrosine Kinase Protein Overexpression [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients