Sphenoorbital Meningioma

Preferred Label : Sphenoorbital Meningioma;

NCIt definition : A meningioma that affects the sphenoorbital region.;

Neoplastic status : Undetermined;

Details

Origin ID

C5285;

UMLS CUI

C1336040;

Automatic exact mappings (from CISMeF team)
- sphenoorbital meningioma [DO Concept]
DO Cross reference
- sphenoorbital meningioma [DO Concept]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- Headache [NCIt concept]
- Seizure [NCIt concept]
- Well-Circumscribed Lesion [NCIt concept]
Excludes anatomical site(s)
- Spinal Cord [NCIt concept]
Has associated anatomic sites
- Base of the Skull [NCIt concept]
- Central Nervous System [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Head and Neck [NCIt concept]
- Meninges [NCIt concept]
- Nervous System [NCIt concept]
- Skull [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- sphenoorbital meningioma [DO Concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Meningothelial Cell [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Meningothelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
- Meninges [NCIt concept]
disease_has_primary_anatomic_site
- Base of the Skull [NCIt concept]
- Central Nervous System [NCIt concept]
- Skull [NCIt concept]
- Sphenoorbital Region [NCIt concept]
disease_may_have_cytogenetic_abnormality
- Gain of Chromosome 12q [NCIt concept]
- Gain of Chromosome 15q [NCIt concept]
- Gain of Chromosome 17q [NCIt concept]
- Gain of Chromosome 1q [NCIt concept]
- Gain of Chromosome 20q [NCIt concept]
- Gain of Chromosome 9q [NCIt concept]
- Loss of Chromosome 14 [NCIt concept]
- Loss of Chromosome 1p [NCIt concept]
- Loss of Chromosome 22 [NCIt concept]
- Loss of Chromosome 3p [NCIt concept]
disease_may_have_molecular_abnormality
- AKT1 Gene Mutation [NCIt concept]
- NF2 Gene Inactivation [NCIt concept]
- PIK3CA Gene Mutation [NCIt concept]
- SMO Gene Mutation [NCIt concept]
- TRAF7 Gene Mutation [NCIt concept]

Keyword's position in hierarchy(ies) :

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