Hereditary Meningioma

Preferred Label : Hereditary Meningioma;

NCIt synonyms : Familial Meningioma;

NCIt definition : A meningioma that is transmitted from the parents to an offspring.;

Neoplastic status : Undetermined;

Details

Origin ID

C5301;

UMLS CUI

C1333989;

Automatic exact mappings (from CISMeF team)
- familial meningioma [DO Concept]
- meningioma, familial [MeSH concept]
- meningioma, familial [MeSH Supplementary Concept]
DO Cross reference
- familial meningioma [DO 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]
UMLS correspondences (same concept)
- familial meningioma [DO Concept]
- meningioma, familial [MeSH Supplementary Concept]
- meningioma, familial [MeSH concept]
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
- Hereditary 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]
related_to_genetic_biomarker
- SMARCE1 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients