ORPHA:225686
Peroxisomal disease 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 | Peroxisomal disease with epilepsy | |
| fr | Maladie péroxysomale avec épilepsie | |
| de | Peroxisomale Krankheit mit Epilepsie | |
| es | Enfermedad peroxisomal con epilepsia | |
| it | Malattia perossisomiale associata a epilessia | |
| nl | Peroxisomale ziekte met epilepsie | |
| pt | Doença peroxissomal com epilepsia | |
| pl | Choroba peroksysomalna z padaczką | |
| cs | Peroxizomální onemocnění s epilepsií | |
| uk | Пероксисомальна хвороба з епілепсією | |
| zh | 过氧化物酶体病伴癫痫 | |
| tr | Epilepsi ile seyreden peroksizomal hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16398 | E | validated | |
| UMLS | C5680899 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:166481Metabolic diseases with epilepsy
rare genetic diseases; 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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/225686
- This record as JSON: /data/d/225686.json