loading...| Preferred Name | Oligodendroglioma | |
| Synonyms |
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| Definitions |
A rare glial tumor characterized by a highly cellular lesion that is diffusly infiltrating at the periphery and consists of evenly-spaced monomorphic cells with the oligodendroglial phenotype. It typically occurs in the supratentorial white matter. Histologically, the cells are uniformly round to oval with round nuclei, delicate chromatin and small nucleoli. Most patients present with seizures. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_251627 |
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| definition |
A rare glial tumor characterized by a highly cellular lesion that is diffusly infiltrating at the periphery and consists of evenly-spaced monomorphic cells with the oligodendroglial phenotype. It typically occurs in the supratentorial white matter. Histologically, the cells are uniformly round to oval with round nuclei, delicate chromatin and small nucleoli. Most patients present with seizures. |
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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=251627 |
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| has_age_of_onset |
All ages |
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| has_inheritance |
Not applicable |
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| hasDbXref |
MeSH:D009837 ICD-11:2A00.0Y ICD-11:XH7W59 OMIM:137800 MedDRA:10030286 ICD-10:C71.9 UMLS:C0028945 ICD-11:XH7K31 |
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| label |
Oligodendroglioma |
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| notation |
ORPHA:251627 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_251627 |
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| prefLabel |
Oligodendroglioma |
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| present_in |
Europe AND has_annual_incidence_average_value : 0.25 AND has_annual_incidence_range : 1-9 / 1 000 000 |
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| treeView | ||
| subClassOf |