Sellar Chondroid Chordoma

Preferred Label : Sellar Chondroid Chordoma;

NCIt definition : A chondroid chordoma that arises from the sellar region.;

Neoplastic status : Malignant;

NCI Metathesaurus CUI : CL556261;

Details

Origin ID

C155782;

UMLS CUI

C4744375;

Disease excludes normal cell origin
- Bone Marrow Stem Cell [NCIt concept]
Disease may have findings
- Headache [NCIt concept]
Excludes anatomical site(s)
- Spinal Cord [NCIt concept]
Has associated anatomic sites
- Base of the Skull [NCIt concept]
- Bone [NCIt concept]
- Central Nervous System [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Head and Neck [NCIt concept]
- Musculoskeletal System [NCIt concept]
- Nervous System [NCIt concept]
- Sellar Region [NCIt concept]
- Skull [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- High Grade Lesion [NCIt concept]
- Indolent Clinical Course [NCIt concept]
- Sarcomatous Component Present [NCIt concept]
disease_excludes_normal_tissue_origin
- Germinal Layer [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Malignant Epithelioid Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Physaliphorous Cell [NCIt concept]
disease_has_finding
- Cartilage-Like Elements Present [NCIt concept]
- Lobulated Growth Pattern [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
- Myxoid Stroma Formation [NCIt concept]
- Slow Growing Mass [NCIt concept]
- Solitary Mass [NCIt concept]
disease_has_normal_cell_origin
- Embryonic Cell [NCIt concept]
disease_has_normal_tissue_origin
- Embryonic Tissue [NCIt concept]
- Remnants of the Notochord [NCIt concept]
disease_has_primary_anatomic_site
- Base of the Skull [NCIt concept]
- Bone [NCIt concept]
- Central Nervous System [NCIt concept]
- Sellar Region [NCIt concept]
disease_mapped_to_gene
- CDKN2A Gene [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 20 [NCIt concept]
- Gain of Chromosome 5q [NCIt concept]
- Gain of Chromosome 7q [NCIt concept]
- Loss of Chromosome 10 [NCIt concept]
- Loss of Chromosome 13 [NCIt concept]
- Loss of Chromosome 3 [NCIt concept]
- Loss of Chromosome 4 [NCIt concept]
disease_may_have_molecular_abnormality
- CDKN2A Gene Deletion [NCIt concept]

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