Askin Tumor - CISMeF

Preferred Label : Askin Tumor;

NCIt synonyms : Small Cell Tumor of Thoracopulmonary Region; Peripheral Neuroectodermal Tumor of Thoracopulmonary Region; Askin's Tumor; PNET of Thoracopulmonary Region; Askin s Tumor;

NCIt definition : A primitive neuroectodermal tumor (small round blue cell tumor) of the thorax which can involve the periosteum, thoracic wall and/or pleura though it spares the lung parenchyma.;

Neoplastic status : Malignant;

ICD-O code : 9365/3;

Détails

Origin ID

C7542;

UMLS CUI

C0877849;

Automatic exact mappings (from CISMeF team)
- Adenolymphoma (disorder) [SNOMED CT concept]
- Adenolymphoma (morphologic abnormality) [SNOMED CT concept]
- Askin tumour [ICD-11 Extension code]
- 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 sarcoma [DO Concept]
- Ewing sarcoma [OMIM Phenotype]
- Ewing's sarcoma [MedDRA Preferred Term]
- Ewing's sarcoma (morphologic abnormality) [SNOMED CT concept]
- Ewing's tumor [MedDRA LLT]
- Granular cell tumor (disorder) [SNOMED CT concept]
- Juvenile aponeurotic fibroma (morphologic abnormality) [SNOMED CT concept]
- Klatskin Tumor [MeSH Descriptor]
- Klatskin's tumor (disorder) [SNOMED CT concept]
- Klatskin's tumor (morphologic abnormality) [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]
- Trichoepithelioma (disorder) [SNOMED CT concept]
- Trichoepithelioma (morphologic abnormality) [SNOMED CT concept]
- Ungual fibroma [HPO term]
- Warthin's tumor [MedDRA LLT]
- abrikosov's tumor [MeSH concept]
- abrikosov's tumor [MeSH Supplementary Concept]
- burkitt lymphoma [MeSH Descriptor]
- klatskin's tumor [SNOMED Notion]
- krukenberg tumor [MeSH Descriptor]
- sarcoma, ewing [MeSH Descriptor]
- wilms tumor [MeSH Descriptor]
Currated CISMeF NLP mapping
- Askin Tumor [Disease (Nov.)]
- Askin tumor [ICD-O code]
- Askin tumor (morphologic abnormality) [SNOMED CT concept]
- Askin's tumor [DO Concept]
- Askin's tumor [MedDRA LLT]
- Askin's tumour [MedDRA LLT]
- Small cell sarcoma (morphologic abnormality) [SNOMED CT concept]
- askin tumor [MeSH concept]
- askin tumor [MeSH Supplementary Concept]
DO Cross reference
- Ewing sarcoma [DO Concept]
Disease may have findings
- Fever [NCIt concept]
- Hemorrhagic Change [NCIt concept]
- Homer Wright Rosette Formation [NCIt concept]
- Necrotic Change [NCIt concept]
Has associated anatomic sites
- Nervous System [NCIt concept]
- Thoracic Cavity [NCIt concept]
Has cytogenetic abnormalities
- EWSR1 Gene Rearrangement [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Askin Tumor [Disease (Nov.)]
- Askin tumor [ICD-O code]
- Askin tumor (morphologic abnormality) [SNOMED CT concept]
- Askin's tumor [MedDRA LLT]
- Askin's tumour [MedDRA LLT]
- askin tumor [MeSH Supplementary Concept]
- askin tumor [MeSH concept]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease 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]
disease_excludes_cytogenetic_abnormality
- CIC Gene Rearrangement [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [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
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Neuroectodermal Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Primitive Round to Oval Cell [NCIt concept]
disease_has_finding
- Malignant Cellular Infiltrate [NCIt concept]
- Neuroectodermal Differentiation [NCIt concept]
disease_has_normal_cell_origin
- Embryonic Cell [NCIt concept]
- Neuroectodermal Cell [NCIt concept]
disease_has_normal_tissue_origin
- Embryonic Tissue [NCIt concept]
- Neural Crest [NCIt concept]
- Neuroectoderm [NCIt concept]
disease_has_primary_anatomic_site
- Peripheral Nerve [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]

Position du mot-clé dans l'(les) arborescence(s) :

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