Childhood Synovial Sarcoma

Preferred Label : Childhood Synovial Sarcoma;

NCIt synonyms : Pediatric Synovial Sarcoma;

NCIt related terms : Synovial Sarcoma;

NCIt definition : A synovial sarcoma occurring in childhood.;

Alternative definition : NICHD: A synovial sarcoma occurring during childhood.;

Neoplastic status : Malignant;

Details

Origin ID

C8089;

UMLS CUI

C0279982;

Automatic exact mappings (from CISMeF team)
- SSX family member 2 [HGNC gene]
- Sarcoma, synovial [OMIM Phenotype]
- Synovial sarcoma [PASCAL descriptor]
- Synovial sarcoma [HPO term]
- Synovial sarcoma [MedDRA Preferred Term]
- Synovial sarcoma [ORDO Disease]
- Synovial sarcoma (disorder) [SNOMED CT concept]
- Synovial sarcoma (morphologic abnormality) [SNOMED CT concept]
- sarcoma, synovial [MeSH Descriptor]
- sarcoma, synovial [MeSH concept]
- synovial sarcoma [DO Concept]
- synovial sarcoma [Radlex concept]
Disease excludes normal cell origin
- Epithelial Cell [NCIt concept]
Excludes anatomical site(s)
- Bone [NCIt concept]
Has associated anatomic sites
- Connective and 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]
- Neoplastic Cell [NCIt concept]
disease_has_finding
- Childhood Lesion [NCIt concept]
- High Grade Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Metastatic/Recurrent Disease [NCIt concept]
- Tissue Differentiation Uncertain [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Soft Tissue [NCIt concept]
disease_mapped_to_gene
- SS18 Gene [NCIt concept]
- SS18/SSX1 Fusion Gene [NCIt concept]
- SS18/SSX2 Fusion Gene [NCIt concept]
- SS18/SSX4 Fusion Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- t(X;18)(p11;q11) [NCIt concept]
disease_may_have_molecular_abnormality
- SS18-SSX1 Fusion Protein Expression [NCIt concept]
- SS18-SSX2 Fusion Protein Expression [NCIt concept]
- SS18-SSX4 Fusion Protein Expression [NCIt concept]

Keyword's position in hierarchy(ies) :

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