Ewing Sarcoma - CISMeF

Preferred Label : Ewing Sarcoma;

NCIt synonyms : Ewing's Sarcoma; ES; Ewing's Tumor; Ewing s Sarcoma;

NCIt related terms : Ewing tumor;

NCIt definition : A small round cell tumor that lacks morphologic, immunohistochemical, and electron microscopic evidence of neuroectodermal differentiation. It represents one of the two ends of the spectrum called Ewing sarcoma/peripheral neuroectodermal tumor. It affects mostly males under age 20, and it can occur in soft tissue or bone. Pain and the presence of a mass are the most common clinical symptoms.;

Alternative definition : NICHD: A malignant neoplasm of the bone, or the soft tissue adjacent to bone, that is comprised of primitive neuroectodermal cells.; NCI-GLOSS: A type of cancer that forms in bone or soft tissue.;

Neoplastic status : Malignant;

ICD-O code : 9260/3;

Codes from synonyms : CDR0000046031;

Details

Origin ID

C4817;

UMLS CUI

C0553580;

Automatic exact mappings (from CISMeF team)
- Adenolymphoma (disorder) [SNOMED CT concept]
- Adenolymphoma (morphologic abnormality) [SNOMED CT concept]
- Askin tumor (morphologic abnormality) [SNOMED CT concept]
- Askin's tumor [MedDRA LLT]
- B-cell type acute leukaemia [MedDRA Preferred Term]
- Burkitt lymphoma (morphologic abnormality) [SNOMED CT concept]
- Burkitt's lymphoma (disorder) [SNOMED CT concept]
- Burkitt's tumor [MedDRA LLT]
- Castleman Disease [MeSH Descriptor]
- Chondroblastoma (morphologic abnormality) [SNOMED CT concept]
- Eccrine dermal cylindroma of skin (disorder) [SNOMED CT concept]
- Ewing tumor [ACR pathology]
- Ewing tumor [ACR pathology]
- Ewing tumor [ACR pathology]
- Ewing tumor [ACR pathology]
- Ewing's sarcoma [ICD-9 code]
- Granular cell tumor (disorder) [SNOMED CT concept]
- Hodgkin sarcoma [obs] (morphologic abnormality) [SNOMED CT concept]
- Hodgkin's sarcoma [MedDRA LLT]
- Hodgkin's sarcoma (disorder) [SNOMED CT concept]
- Juvenile aponeurotic fibroma (morphologic abnormality) [SNOMED CT concept]
- Kaposi sarcoma [ORDO Disease]
- Kaposi's sarcoma [MedDRA Preferred Term]
- Kaposi's sarcoma [HRDO Sign]
- Kaposi's sarcoma [HPO term]
- Kaposi's sarcoma (disorder) [SNOMED CT concept]
- Kaposi's sarcoma, morphology (morphologic abnormality) [SNOMED CT concept]
- Klatskin Tumor [MeSH Descriptor]
- Klatskin's tumor (disorder) [SNOMED CT concept]
- Klatskin's tumor (morphologic abnormality) [SNOMED CT concept]
- Lower case Roman letter e (qualifier value) [SNOMED CT concept]
- Nephroblastoma [HPO term]
- Pancoast's tumor [MedDRA LLT]
- Pancoast's tumour [MedDRA Preferred Term]
- Papillary intralymphatic angioendothelioma of childhood (disorder) [SNOMED CT concept]
- Small cell sarcoma (morphologic abnormality) [SNOMED CT concept]
- Trichoepithelioma (disorder) [SNOMED CT concept]
- Trichoepithelioma (morphologic abnormality) [SNOMED CT concept]
- Ungual fibroma [HPO term]
- Upper case Roman letter E (qualifier value) [SNOMED CT concept]
- Warthin's tumor [MedDRA LLT]
- abrikosov's tumor [MeSH concept]
- abrikosov's tumor [MeSH Supplementary Concept]
- bone cancer [MedlinePlus Topic]
- burkitt lymphoma [MeSH Descriptor]
- ethics [MeSH Descriptor]
- hodgkin's sarcoma [SNOMED Notion]
- kaposi sarcoma [MedlinePlus Topic]
- kaposi's sarcoma [SNOMED Notion]
- klatskin's tumor [SNOMED Notion]
- krukenberg tumor [MeSH Descriptor]
- sarcoma, kaposi [MeSH Descriptor]
- wilms tumor [MeSH Descriptor]
Currated CISMeF NLP mapping
- Ewing sarcoma [PASCAL descriptor]
- Ewing sarcoma [DO Concept]
- Ewing sarcoma [Disease (Nov.)]
- Ewing sarcoma [HPO term]
- Ewing sarcoma [ICD-11 Extension code]
- Ewing sarcoma [Radlex concept]
- Ewing sarcoma [OMIM Phenotype]
- Ewing sarcoma [ICD-O code]
- Ewing's sarcoma [MedDRA Preferred Term]
- Ewing's sarcoma (morphologic abnormality) [SNOMED CT concept]
- Ewing's sarcoma NOS [MedDRA LLT]
- Ewing's tumor [MedDRA LLT]
- Ewing's tumour [MedDRA LLT]
- Skeletal Ewing sarcoma [ORDO Disease]
- ewing sarcoma [ICD-O menu]
- ewing's sarcoma [SNOMED Notion]
- sarcoma, ewing [MeSH Descriptor]
- sarcoma, ewing [MeSH concept]
DO Cross reference
- Ewing sarcoma [DO Concept]
Disease excludes normal cell origin
- Epithelial Cell [NCIt concept]
Disease may have findings
- Fever [NCIt concept]
- Hemorrhagic Change [NCIt concept]
- Homer Wright Rosette Formation [NCIt concept]
- Necrotic Change [NCIt concept]
False automatic mappings
- (Cort-Co)-E [MeSH concept]
Has associated anatomic sites
- Connective and Soft Tissue [NCIt concept]
Has cytogenetic abnormalities
- EWSR1 Gene Rearrangement [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Ewing sarcoma [OMIM Phenotype]
- Ewing sarcoma [ICD-O code]
- Ewing sarcoma [HPO term]
- Ewing sarcoma [Radlex concept]
- Ewing sarcoma [PASCAL descriptor]
- Ewing sarcoma [DO Concept]
- Ewing sarcoma [Disease (Nov.)]
- Ewing's sarcoma [MedDRA Preferred Term]
- Ewing's sarcoma (morphologic abnormality) [SNOMED CT concept]
- Ewing's sarcoma NOS [MedDRA LLT]
- Ewing's sarcoma stage unspecified [MedDRA LLT]
- Ewing's tumor [MedDRA LLT]
- Ewing's tumour [MedDRA LLT]
- Skeletal Ewing sarcoma [ORDO Disease]
- ewing sarcoma [ICD-O menu]
- ewing's sarcoma [SNOMED Notion]
- sarcoma, ewing [MeSH Descriptor]
- sarcoma, ewing [MeSH concept]
associated_with_malfunction_of_gene_product
- G Antigen Family D Member 3 [NCIt concept]
concept_is_in_subset
- CPTAC Codelists Terminology [NCIt concept]
- CPTAC Neoplasms Codelist [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- CTS-API Disease Main Type Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- Clinical Trials Search-Application Programming Interface Disease Category Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.1 Morphology Terminology [NCIt concept]
- Mapped ICDO3.1 Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology PT Terminology [NCIt concept]
- Mapped ICDO3.2 Morphology Terminology [NCIt concept]
- Mapped ICDO3.2 Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Adverse Events Terminology [NCIt concept]
- Pediatric Adverse Events Terminology Mapped to MedDRA [NCIt concept]
disease_excludes_cytogenetic_abnormality
- CIC Gene Rearrangement [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]
- Neuroectodermal Differentiation [NCIt concept]
disease_excludes_molecular_abnormality
- EWSR1-NFATC2 Fusion Protein Expression [NCIt concept]
- EWSR1-PATZ1 Fusion Protein Expression [NCIt concept]
- FUS-NFATC2 Fusion Protein Expression [NCIt concept]
disease_excludes_normal_tissue_origin
- Epithelial Tissue [NCIt concept]
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Primitive Round to Oval Cell [NCIt concept]
disease_has_finding
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_normal_cell_origin
- Embryonic Cell [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Embryonic Tissue [NCIt concept]
- Neural Crest [NCIt concept]
disease_mapped_to_gene
- EWSR1 Gene [NCIt concept]
- EWSR1/ERG Fusion Gene [NCIt concept]
- EWSR1/ETV1 Fusion Gene [NCIt concept]
- EWSR1/ETV4 Fusion Gene [NCIt concept]
- EWSR1/FEV Fusion Gene [NCIt concept]
- EWSR1/FLI1 Fusion Gene [NCIt concept]
- FUS/ERG Fusion Gene [NCIt concept]
disease_may_have_abnormal_cell
- Malignant Small Round Cell [NCIt concept]
disease_may_have_associated_disease
- Anemia [NCIt concept]
disease_may_have_cytogenetic_abnormality
- inv(22q12) [NCIt concept]
- t(11;22)(q24;q12) [NCIt concept]
- t(16;21)(p11;q22) [NCIt concept]
- t(17;22)(q21;q12) [NCIt concept]
- t(1;22)(p36.1;q12) [NCIt concept]
- t(21;22)(q22;q12) [NCIt concept]
- t(2;22)(q33;q12) [NCIt concept]
- t(7;22)(p22;q12) [NCIt concept]
disease_may_have_molecular_abnormality
- EWSR1-ERG Fusion Protein Expression [NCIt concept]
- EWSR1-ETV1 Fusion Protein Expression [NCIt concept]
- EWSR1-ETV4 Fusion Protein Expression [NCIt concept]
- EWSR1-FEV Fusion Protein Expression [NCIt concept]
- EWSR1-FLI1 Fusion Protein Expression [NCIt concept]
- FUS-ERG Fusion Protein Expression [NCIt concept]
may_be_associated_disease_of_disease
- Hereditary Retinoblastoma [NCIt concept]
neoplasm_has_special_category
- Solid Neoplasm [NCIt concept]

Keyword's position in hierarchy(ies) :

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