Chordoid Meningioma

Preferred Label : Chordoid Meningioma;

NCIt definition : A WHO grade II, usually recurring meningioma characterized by the predominance of tissues that are histologically similar to chordoma.;

Neoplastic status : Undetermined;

Détails

Origin ID

C6908;

UMLS CUI

C1370510;

Automatic exact mappings (from CISMeF team)
- Chordoid meningioma [ICD-11 Extension code]
- Clear cell meningioma (morphologic abnormality) [SNOMED CT concept]
- Meningioma, chordoid (morphologic abnormality) [SNOMED CT concept]
- chordoid meningioma [DO Concept]
- papillary meningioma [SNOMED Notion]
Currated CISMeF NLP mapping
- chordoid meningioma [Radlex concept]
DO Cross reference
- chordoid meningioma [DO Concept]
Disease excludes normal cell origin
- Neuron, Neuroepithelial Cell, and Supporting Cell of the Nervous System [NCIt concept]
Disease may have findings
- Chronic Inflammatory Infiltrate [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)
- Meningioma, chordoid (morphologic abnormality) [SNOMED CT concept]
- chordoid meningioma [Radlex concept]
- chordoid meningioma [DO Concept]
concept_is_in_subset
- GDC Terminology [NCIt concept]
- GDC Value Terminology [NCIt concept]
- NCIt Neoplasm Core Terminology [NCIt concept]
disease_has_abnormal_cell
- Eosinophilic Meningothelial Cell [NCIt concept]
- Neoplastic Cell [NCIt concept]
- Neoplastic Connective and Soft Tissue Cell [NCIt concept]
- Neoplastic Meningothelial Cell [NCIt concept]
disease_has_finding
- Myxoid Stroma Formation [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
- Meninges [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
disease_may_have_associated_disease
- Castleman Disease [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]

Position du mot-clé dans l'(les) arborescence(s) :

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