Anaplastic (Malignant) Meningioma

Preferred Label : Anaplastic (Malignant) Meningioma;

NCIt synonyms : Anaplastic Meningioma; Anaplastic Malignant Meningioma;

NCIt related terms : Meningioma, anaplastic;

NCIt definition : A WHO grade 3 meningioma characterized by the presence of malignant morphologic features, including malignant cytology and a very high mitotic index (20 or more mitoses per ten high power fields).;

Neoplastic status : Malignant;

ICD-O code : 9530/3;

Details

Origin ID

C4051;

UMLS CUI

C0259785;

Automatic exact mappings (from CISMeF team)
- Meningioma, malignant [ICD-9 code]
- Meningioma, malignant [ICD-11 Extension code]
- Meningiomas, malignant [Bloc CIM-11]
- meningioma [MeSH Descriptor]
Currated CISMeF NLP mapping
- Anaplastic meningioma [MedDRA Preferred Term]
- Malignant meningioma [PASCAL descriptor]
- Malignant meningioma [MedDRA LLT]
- Meningioma malignant [MedDRA Preferred Term]
- Meningioma malignant NOS [MedDRA LLT]
- Meningioma, malignant [ICD-O code]
- Meningioma, malignant (morphologic abnormality) [SNOMED CT concept]
- Meningiomas malignant [MedDRA High Level Term]
- anaplastic meningioma [Disease (Nov.)]
- anaplastic meningioma [Radlex concept]
- malignant meningioma [MeSH concept]
- meningioma, malignant [SNOMED Notion]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- High Mitotic Activity [NCIt concept]
- 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]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Anaplastic meningioma [MedDRA Preferred Term]
- Malignant meningioma [PASCAL descriptor]
- Malignant meningioma [MedDRA LLT]
- Meningioma malignant [MedDRA Preferred Term]
- Meningioma malignant NOS [MedDRA LLT]
- Meningioma, malignant [ICD-O code]
- Meningioma, malignant (morphologic abnormality) [SNOMED CT concept]
- Meningiomas malignant [MedDRA High Level Term]
- anaplastic meningioma [Radlex concept]
- anaplastic meningioma [Disease (Nov.)]
- malignant meningioma [Disease (Nov.)]
- malignant meningioma [MeSH concept]
- meningioma, malignant [SNOMED Notion]
Validated automatic mappings to NTBT
- malignant meningioma [Disease (Nov.)]
concept_is_in_subset
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
disease_excludes_finding
- Benign Cellular Infiltrate [NCIt concept]
- Indolent Clinical Course [NCIt concept]
disease_has_abnormal_cell
- Malignant Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Meningothelial Cell [NCIt concept]
disease_has_finding
- Anaplastic Lesion [NCIt concept]
- Malignant Cellular Infiltrate [NCIt concept]
disease_has_grade
- Grade 3 [NCIt concept]
disease_has_normal_cell_origin
- Connective and Soft Tissue Cell [NCIt concept]
- Meningothelial Cell [NCIt concept]
disease_has_normal_tissue_origin
- Meninges [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Connective and Soft Tissue [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
- CDKN2A Gene Deletion [NCIt concept]
- CDKN2B Gene Deletion [NCIt concept]
- NF2 Gene Inactivation [NCIt concept]
- TERT Promoter Mutation [NCIt concept]

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