ORPHA:98516
Malformation of the cerebellar hemispheres
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Malformation of the cerebellar hemispheres | |
| fr | Malformation des hémisphères cérébelleux | |
| de | Fehlbildung der zerebellären Hemisphären | |
| es | Malformación de los hemisferios del cerebelo | |
| it | Malformazione degli emisferi cerebellari | |
| nl | Malformatie van cerebellaire hemisferen | |
| pt | Malformação dos hemisférios do cerebelo | |
| pl | Malformacja półkul móżdżku | |
| cs | Malformace mozečkových hemisfér | |
| uk | Вади розвитку півкуль мозочка | |
| zh | 小脑半球畸形 | |
| tr | Serebellar hemisferlerin malformasyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681736 | 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:729527Isolated cerebellar malformation
rare developmental anomalies during embryogenesis; rare neurological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
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/98516
- This record as JSON: /data/d/98516.json