Preferred Label : Clear Cell Sarcoma of the Kidney;
NCIt synonyms : Childhood Kidney Clear Cell Sarcoma; CCSK; Renal Clear Cell Sarcoma; Kidney Clear Cell Sarcoma; Childhood Clear Cell Sarcoma of the Kidney; Childhood Renal Clear Cell Sarcoma; Pediatric Kidney Clear Cell Sarcoma; Pediatric Renal Clear Cell Sarcoma;
NCIt related terms : Clear cell sarcoma of the kidney (CCSK); Clear cell sarcoma - kidney; Clear cell sarcoma of kidney;
NCIt definition : A rare pediatric sarcoma affecting the kidney. It is characterized by the presence
of epithelioid or spindle cells forming cords or nests, separated by fibrovascular
septa. It metastasizes to lung, bone, brain and soft tissue.;
Alternative definition : NICHD: A rare primary renal tumor characterized by nests or cords of cells that are
separated by regularly spaced fibrovascular septa, and which are known to metastasize
to lung, bone, brain and soft tissue. It is associated with internal tandem duplications
in the BCOR gene.; NCI-GLOSS: A rare type of kidney cancer, in which the inside of the cells look clear
when viewed under a microscope. Clear cell sarcoma can spread from the kidney to other
organs, most commonly the bone, but also including the lungs, brain, and soft tissues
of the body.;
Neoplastic status : Malignant;
ICD-O code : 8964/3;
Codes from synonyms : 10009253; CDR0000044997;
Origin ID : C4264;
UMLS CUI : C0334488;
Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- DO Cross reference
- Disease excludes normal cell origin
- Excludes anatomical site(s)
- Has associated anatomic sites
- Semantic type(s)
- UMLS correspondences (same concept)
- concept_is_in_subset
- disease_excludes_finding
- disease_excludes_normal_tissue_origin
- disease_has_abnormal_cell
- disease_has_finding
- disease_has_normal_tissue_origin
- disease_has_primary_anatomic_site
- disease_mapped_to_gene
- disease_may_have_abnormal_cell
- disease_may_have_cytogenetic_abnormality
- disease_may_have_molecular_abnormality
- pathogenesis_of_disease_involves_gene
