Sacral Intraspinal Meningioma

Preferred Label : Sacral Intraspinal Meningioma;

NCIt synonyms : Meningioma of Sacral Spinal Canal and Spinal Cord; Sacral Spinal Canal and Spinal Cord Meningioma; Meningioma of the Sacral Spinal Canal and Spinal Cord;

NCIt definition : A meningioma that arises from the meninges of the sacral region of the spinal cord.;

Neoplastic status : Undetermined;

Details

Origin ID

C5299;

UMLS CUI

C1335893;

Automatic exact mappings (from CISMeF team)
- sacral spinal canal and spinal cord meningioma [DO Concept]
DO Cross reference
- sacral spinal canal and spinal cord meningioma [DO Concept]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- Well-Circumscribed Lesion [NCIt concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Meninges [NCIt concept]
- Nervous System [NCIt concept]
- Sacrum [NCIt concept]
- Spinal Region [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- sacral spinal canal and spinal cord 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]
- Spinal Meninges [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Sacral Vertebra [NCIt concept]
disease_mapped_to_gene
- NF2 Gene [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 22q [NCIt concept]
- Loss of Chromosome 3p [NCIt concept]
disease_may_have_molecular_abnormality
- NF2 Gene Inactivation [NCIt concept]
- NF2 Gene Mutation [NCIt concept]

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