loading...| Preferred Name |
Astroblastoma |
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| Synonyms |
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| Definitions |
A very rare glial neoplasm of the central nervous system, most often with an intra-axial peripheral supratentorial location in one hemisphere of the frontal or parietal lobes and usually presenting in infants and young adults with symptoms of vomiting, loss of consciousness, epileptic seizures and headaches. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_251679 |
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| definition |
A very rare glial neoplasm of the central nervous system, most often with an intra-axial peripheral supratentorial location in one hemisphere of the frontal or parietal lobes and usually presenting in infants and young adults with symptoms of vomiting, loss of consciousness, epileptic seizures and headaches. |
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| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=251679 |
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| has_age_of_onset |
Adolescent Adult Childhood Infancy |
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| has_inheritance |
Not applicable |
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| hasDbXref |
ICD-11:2A00.4 ICD-10:C71.9 UMLS:C0334587 MedDRA:10079366 |
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| label |
Astroblastoma |
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| notation |
ORPHA:251679 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_251679 |
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| prefLabel |
Astroblastoma |
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| present_in |
Europe AND has_annual_incidence_average_value : 0.02 AND has_annual_incidence_range : <1 / 1 000 000 |
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| treeView | ||
| subClassOf |