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Orphanet Rare Disease Ontology
Last uploaded:
December 4, 2024
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| Id | http://www.orpha.net/ORDO/Orphanet_251646
http://www.orpha.net/ORDO/Orphanet_251646
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|---|---|
| Preferred Name | Anaplastic ependymoma |
| Definitions |
A rare, malignant type of ependymoma that most often arises in the supratentorial region of the brain of children and young adults and that manifests with variable symptoms including headaches, nausea, vision impairment, memory loss and difficulty walking.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition_citation | Orphanet |
|---|---|
| definition | A rare, malignant type of ependymoma that most often arises in the supratentorial region of the brain of children and young adults and that manifests with variable symptoms including headaches, nausea, vision impairment, memory loss and difficulty walking. |
| label |
Anaplastic ependymoma
|
| prefLabel |
Anaplastic ependymoma
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| hasDbXref |
UMLS:C0280788
ICD-11:2A00.0Y
ICD-11:XH6922
ICD-10:C71.9
MedDRA:10014968
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| notation |
ORPHA:251646
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| present_in |
United States AND has_annual_incidence_average_value : 0.04 AND has_annual_incidence_range : <1 / 1 000 000
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| part_of | |
| prefixIRI |
ORDO:Orphanet_251646
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| expertlink | |
| subClassOf | |
| type | |
| has_inheritance |
Not applicable
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| has_age_of_onset |
Adolescent
Adult
Childhood
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| treeView |
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