ORPHA:166487
Cerebral diseases of vascular origin with epilepsy
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cerebral diseases of vascular origin with epilepsy | |
| fr | Maladie vasculaire cérébrale associée à une épilepsie | |
| de | Zerebrale Gefäßkrankheiten mit Epilepsie | |
| es | Enfermedades cerebrales de origen vascular con epilepsia | |
| it | Malattie cerebrali di origine vascolare con epilessia | |
| nl | Cerebrale ziektes van vasculaire oorsprong met epilepsie | |
| pt | Doença cerebral vascular com epilepsia | |
| pl | Choroba mózgu pochodzenia naczymiowego z padaczką | |
| cs | Mozkové nemoci cévního původu s epilepsií | |
| uk | Церебральні захворювання судинного походження з епілепсією | |
| zh | 血管源性脑疾病伴癫痫 | |
| tr | Epilepsi ile seyreden vasküler kökenli serebral hastalıklar |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15658 | E | validated | |
| UMLS | C5680434 | 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 (2):
- ORPHA:101998Rare epilepsy
rare neurological diseases - ORPHA:183512Rare genetic epilepsy
rare genetic diseases
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/166487
- This record as JSON: /data/d/166487.json