ORPHA:251867
Classic medulloblastoma
- Type
- Histopathological subtype
- Group
- Subtype of disorder
- Age of onset
- Childhood
- Status
- active
Classic medulloblastoma is a histological variant of medulloblastoma ,an embryonic malignancy, having a midline location, occurring most often in children and manifesting with variable symptoms such as headaches, nausea, vomiting and ataxia.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Classic medulloblastoma | |
| fr | Médulloblastome classique | |
| de | Medulloblastom, klassisches | |
| es | Meduloblastoma clásico | |
| it | Medulloblastoma classico | |
| nl | Klassiek medulloblastoom | |
| pt | Meduloblastoma clássico | |
| pl | Rdzeniak zarodkowy klasyczny | |
| cs | Klasický meduloblastom | |
| uk | Класична медулобластома | |
| zh | 典型成神经管细胞瘤 | |
| tr | Klasik medulloblastom |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 155255 | NTBT | validated | |
| ICD-10 | C71.6 | NTBT | attributed | validated |
| ICD-11 | 2A00.10 | NTBT | index | validated |
| ICD-11 | XH0RY1 | BTNT | specific | validated |
| ICD-11 | XH3EX1 | BTNT | specific | validated |
| MONDO | 0016712 | E | validated | |
| UMLS | C1707400 | 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/251867
- This record as JSON: /data/d/251867.json