Rhabdoid Meningioma

Preferred Label : Rhabdoid Meningioma;

NCIt definition : A WHO grade III meningioma characterized by the predominant presence of rhabdoid cells forming sheets.;

Neoplastic status : Malignant;

Details

Origin ID

C6909;

UMLS CUI

C0259786;

Automatic exact mappings (from CISMeF team)
- Meningioma, rhabdoid (morphologic abnormality) [SNOMED CT concept]
- Papillary Meningioma [SNOMED Notion]
- Papillary meningioma (morphologic abnormality) [SNOMED CT concept]
- Rhabdoid meningioma [ICD-11 Extension code]
- rhabdoid meningioma [DO Concept]
- rhabdoid meningioma [Radlex concept]
Currated CISMeF NLP mapping
- Rhabdoid meningioma [MedDRA LLT]
DO Cross reference
- rhabdoid 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]
See also inter- (CISMeF)
- papillary meningioma [Disease (Nov.)]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Meningioma, rhabdoid (morphologic abnormality) [SNOMED CT concept]
- Rhabdoid meningioma [MedDRA LLT]
- rhabdoid meningioma [DO Concept]
concept_is_in_subset
- 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]
- Rhabdoid Cell [NCIt concept]
disease_has_finding
- 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
- 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
- BAP1 Gene Mutation [NCIt concept]
- NF2 Gene Inactivation [NCIt concept]
- PBRM1 Gene Mutation [NCIt concept]

Keyword's position in hierarchy(ies) :

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