| Preferred Name |
Meningioma |
| ID |
http://www.orpha.net/ORDO/Orphanet_2495 |
| definition |
A rare, mostly benign, neoplastic disease characterized by a primary tumor of the meninges, usually located intracranially (~90%) but spinal meningiomas occur as well. Clinical symptoms relate to the location of the tumor and may include seizures, focal neurological deficits (sensory-motor or visual symptoms, cranial nerve dysfunction), vascular complications (occlusion of cerebral blood vessels, deep venous thrombosis, pulmonary embolism), chronically increased intracranial pressure neurocognitive impairment and/or loss of bladder/anus sphincter control. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2495 |
| has_age_of_onset |
All ages |
| has_inheritance |
Not applicable |
| hasDbXref |
UMLS:C0025286 ICD-11:2A01.0 MedDRA:10027191 OMIM:606190 ICD-10:D32.9 MeSH:D008579 |
| label |
Meningioma |
| notation |
ORPHA:2495 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_2495 |
| prefLabel |
Meningioma |
| present_in |
Europe AND has_point_prevalence_range : Unknown Germany AND has_annual_incidence_average_value : 4.15 AND has_annual_incidence_range : 1-9 / 100 000 United States AND has_annual_incidence_average_value : 8.14 AND has_annual_incidence_range : 1-9 / 100 000 |
| treeView | |
| subClassOf |