Parachordoma - CISMeF

Preferred Label : Parachordoma;

NCIt definition : A rare, usually benign myoepithelial tumor characterized by the presence of epithelioid, often vacuolated neoplastic cells. Most patients present with painless swelling in the subcutaneous or subfascial soft tissues of the extremities.;

Neoplastic status : Undetermined;

ICD-O code : 9373/1; 9373/0;

Details

Origin ID

C6581;

UMLS CUI

C1266175;

Automatic exact mappings (from CISMeF team)
- Parachordoma [ICD-O code]
- Parachordoma [ICD-11 Extension code]
- parachordoma [DO Concept]
DO Cross reference
- parachordoma [DO 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]
UMLS correspondences (same concept)
- Parachordoma (disorder) [SNOMED CT concept]
- Parachordoma (morphologic abnormality) [SNOMED CT concept]
- parachordoma [DO Concept]
concept_is_in_subset
- 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]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Epithelioid Cell [NCIt concept]
- Neoplastic Myoepithelial Cell [NCIt concept]
disease_has_normal_cell_origin
- Myoepithelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Soft Tissue [NCIt concept]
disease_may_have_cytogenetic_abnormality
- EWSR1 Gene Rearrangement [NCIt concept]
- Loss of Chromosome 17p [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

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