ORPHA:251855
Anaplastic/large cell medulloblastoma
- Type
- Histopathological subtype
- Group
- Subtype of disorder
- Age of onset
- Infancy, Neonatal
- Status
- active
A histological variant of medulloblastoma, an embryonic malignancy, associated with extremely low survival rates and a high risk of metastatic disease and manifesting with symptoms of increased intracranial pressure such as vomiting, headache, listlessness, papilledema and diplopia.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Anaplastic/large cell medulloblastoma | |
| fr | Médulloblastome anaplasique à grandes cellules | |
| de | Medulloblastom, anaplastisches/großzelliges | |
| es | Meduloblastoma anaplásico de células grandes | |
| it | Medulloblastoma anaplastico a grandi cellule | |
| nl | Anaplastisch/grootcellig medulloblastoom | |
| pt | Meduloblastoma de grandes células/anaplásico | |
| pl | Rdzeniak zarodkowy anaplastyczny/olbrzymiokomórkowy | |
| cs | Anaplastický/velkobuněčný meduloblastom | |
| uk | Анапластична/великоклітинна медулобластома | |
| zh | 间变性/大细胞成神经管细胞瘤 | |
| tr | Anaplastik / büyük hücreli medulloblastom |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C71.6 | NTBT | attributed | validated |
| ICD-11 | 2A00.10 | NTBT | index | validated |
| MONDO | 0016709 | E | validated | |
| UMLS | C4330531 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:616Medulloblastoma
rare neurological diseases; rare neoplastic diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/251855
- This record as JSON: /data/d/251855.json