Spinal Multifocal Clear Cell Meningioma

Preferred Label : Spinal Multifocal Clear Cell Meningioma;

NCIt synonyms : Multifocal Clear Cell Meningioma of the Spine; Multifocal Clear Cell Meningioma of Spine;

NCIt definition : A clear cell meningioma arising in multiple areas of the spinal cord characterized by the presence of clear glycogen-rich polygonal cells.;

Neoplastic status : Undetermined;

Details

Origin ID

C5287;

UMLS CUI

C1336051;

Automatic exact mappings (from CISMeF team)
- spinal multifocal clear cell meningioma [DO Concept]
DO Cross reference
- spinal multifocal clear cell meningioma [DO Concept]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- Unfavorable Clinical Outcome [NCIt concept]
- 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]
- Spinal Region [NCIt concept]
- Vertebral Canal [NCIt concept]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- spinal multifocal clear cell meningioma [DO Concept]
disease_has_abnormal_cell
- Meningothelial Cell with Clear Cytoplasm [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Meningothelial Cell [NCIt concept]
disease_has_finding
- Multifocal Lesion [NCIt concept]
disease_has_grade
- Grade 2 [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]
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]
- SMARCE1 Gene Mutation [NCIt concept]

Keyword's position in hierarchy(ies) :

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