Preferred Label : Central Nervous System Mesenchymal, Non-Meningothelial Neoplasm;
NCIt synonyms : Mesenchymal, Non-Meningothelial Tumor of Central Nervous System; Mesenchymal Non-Meningothelial Tumor of the Central Nervous System; Central Nervous System Soft Tissue Tumor; Soft Tissue Neoplasm of Central Nervous System; Soft Tissue Neoplasm of the CNS; Soft Tissue Tumor of the Central Nervous System; CNS Soft Tissue Neoplasm; Mesenchymal, Non-Meningothelial Tumor of CNS; Soft Tissue Tumor of the CNS; Soft Tissue Neoplasm of CNS; Soft Tissue Tumor of CNS; Soft Tissue Neoplasm of the Central Nervous System; CNS Soft Tissue Tumor; Mesenchymal, Non-Meningothelial Tumor of the CNS; Soft Tissue Tumor of Central Nervous System; Central Nervous System Mesenchymal, Non-Meningothelial Tumor; Central Nervous System Soft Tissue Neoplasm;
NCIt definition : A benign or malignant mesenchymal neoplasm originating in the central nervous system
or the meninges and showing fibrous, fibrohistiocytic, adipose, myoid, endothelial,
chondroid or osseous, but not meningothelial differentiation. Depending on the histological
features and clinical behavior of these neoplasms, their grade ranges from benign
(WHO grade I) to highly malignant (WHO grade IV). (Adapted from WHO);
Neoplastic status : Undetermined;
Origin ID : C5449;
UMLS CUI : C1332893;
Automatic exact mappings (from CISMeF team)
- Excludes anatomical site(s)
- Has associated anatomic sites
- Semantic type(s)
- disease_has_abnormal_cell
- disease_has_normal_tissue_origin
- disease_has_primary_anatomic_site
