Childhood Clear Cell Sarcoma of Soft Tissue

Preferred Label : Childhood Clear Cell Sarcoma of Soft Tissue;

NCIt synonyms : Pediatric Clear Cell Sarcoma of Soft Parts; Childhood Clear Cell Sarcoma of Soft Parts;

NCIt related terms : Clear Cell Sarcoma of Soft Tissue;

Alternative definition : NICHD: A clear cell sarcoma of soft tissue occurring in children.;

Neoplastic status : Malignant;

Details

Origin ID

C27371;

UMLS CUI

C1332964;

Automatic exact mappings (from CISMeF team)
- Clear cell sarcoma of soft tissue [MedDRA Preferred Term]
- Melanoma of soft tissue [ORDO Disease]
- sarcoma, clear cell [MeSH Descriptor]
Disease excludes abnormal cell
- Malignant Epithelial Cell [NCIt concept]
Disease excludes normal cell origin
- Epithelial Cell [NCIt concept]
Disease may have findings
- Melanosomes Present [NCIt concept]
- Slow Growing Mass [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]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Intermediate Filaments Present [NCIt concept]
- Intracytoplasmic Eosinophilic Inclusion [NCIt concept]
disease_excludes_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Polygonal Cell with Eosinophilic Cytoplasm [NCIt concept]
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- Fascicular Pattern [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Metastatic/Recurrent Disease [NCIt concept]
- Nested Pattern [NCIt concept]
- Tissue Differentiation Uncertain [NCIt concept]
disease_has_molecular_abnormality
- EWSR1 Gene Rearrangement [NCIt concept]
disease_has_primary_anatomic_site
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
disease_mapped_to_gene
- EWSR1/ATF1 Fusion Gene [NCIt concept]
- EWSR1/CREB1 Fusion Gene [NCIt concept]
disease_may_have_abnormal_cell
- Malignant Spindle Cell [NCIt concept]
- Wreath-Like Multinucleated Giant Cell [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 7 [NCIt concept]
- Gain of Chromosome 8 [NCIt concept]
- t(12;22)(q13;q12) [NCIt concept]
- t(2;22)(q34;q12) [NCIt concept]
disease_may_have_molecular_abnormality
- EWSR1-ATF1 Fusion Protein Expression [NCIt concept]
- EWSR1-CREB1 Fusion Protein Expression [NCIt concept]

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