Adult Meningioma

Preferred Label : Adult Meningioma;

NCIt related terms : Meningioma;

NCIt definition : A meningioma that occurs during adulthood.;

Neoplastic status : Undetermined;

Details

Origin ID

C9093;

UMLS CUI

C0278877;

Automatic exact mappings (from CISMeF team)
- Meningioma [ORDO Disease]
- Meningioma [HPO term]
- Meningioma [MedDRA Preferred Term]
- Meningioma [HRDO Sign]
- Meningioma [PASCAL descriptor]
- Meningioma, benign, no International Classification of Diseases for Oncology subtype (morphologic abnormality) [SNOMED CT concept]
- Meningiomas [Bloc CIM-11]
- brain tumors [MedlinePlus Topic]
- meningioma [DO Concept]
- meningioma [MeSH concept]
- meningioma [ICD-O menu]
- meningioma [MeSH Descriptor]
- meningioma [Radlex 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]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
disease_has_abnormal_cell
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Meningothelial Cell [NCIt concept]
disease_has_finding
- Adulthood Lesion [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
- Central Nervous System [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
- NF2 Gene Inactivation [NCIt concept]

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