Benign PEComa - CISMeF

Preferred Label : Benign PEComa;

NCIt synonyms : Benign PEComa, NOS; Benign PEComa, Not Otherwise Specified; Typical PEComa;

NCIt definition : A tumor with perivascular epithelioid cell differentiation characterized by the absence of pleomorphism and scarcity or absence of mitotic figures.;

Neoplastic status : Benign;

Détails

Origin ID

C121791;

UMLS CUI

C3839685;

Automatic exact mappings (from CISMeF team)
- Perivascular epithelioid tumor, benign (morphologic abnormality) [SNOMED CT concept]
- Perivascular epithelioid tumour, benign [ICD-11 Extension code]
Currated CISMeF NLP mapping
- Benign perivascular epithelioid cell neoplasm (disorder) [SNOMED CT concept]
Disease excludes abnormal cell
- Malignant Cell [NCIt concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Perivascular epithelioid tumor, benign (morphologic abnormality) [SNOMED CT concept]
concept_is_in_subset
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
disease_excludes_finding
- Cellular Pleomorphism [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Mitotic Activity [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Perivascular Epithelioid Cell [NCIt concept]
disease_has_finding
- Benign Cellular Infiltrate [NCIt concept]
- HMB-45-Positive Neoplastic Cells Present [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Perivascular Arrangement of Tumor Cells [NCIt concept]
- S-100-Positive Neoplastic Cells Present [NCIt concept]
- Tissue Differentiation Uncertain [NCIt concept]
disease_has_primary_anatomic_site
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
disease_mapped_to_gene
- TSC2 Gene [NCIt concept]
disease_may_have_molecular_abnormality
- TSC2 Gene Mutation [NCIt concept]

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