ORPHA:166484
Inflammatory and autoimmune 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 | Inflammatory and autoimmune disease with epilepsy | |
| fr | Maladie inflammatoire ou auto-immune associée à une épilepsie | |
| de | Inflammatorische und autoimmune Krankheit mit Epilepsie | |
| es | Enfermedad autoinmune e inflamatoria con epilepsia | |
| it | Malattia infiammatoria e autoimmune con epilessia | |
| nl | Ontstekings- en auto-immuunziekte met epilepsie | |
| pt | Doença autoimune e inflamatória com epilepsia | |
| pl | Choroba zapalna i autoimmunologiczna z padaczką | |
| cs | Zánětlivá autoimunitní onemocnění s epilepsií | |
| uk | Запальні та аутоімунні захворювання з епілепсією | |
| zh | 炎症和自身免疫性疾病伴癫痫 | |
| tr | Epilepsi ile seyreden inflamatuar ve otoimmün hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15657 | E | validated | |
| UMLS | C5680433 | 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:101998Rare epilepsy
rare neurological diseases
Children (11):
- ORPHA:363567Acute encephalopathy with inflammation-mediated status epilepticus
- ORPHA:117Behçet disease
- ORPHA:1459Celiac disease-epilepsy-cerebral calcification syndrome
- ORPHA:900Granulomatosis with polyangiitis
- ORPHA:83467Morvan syndrome
- ORPHA:624166Non-specific autoimmune supratentorial encephalitis with characteristic antibodies
- ORPHA:624178Non-specific autoimmune supratentorial encephalitis without characteristic antibodies
- ORPHA:93552Pediatric systemic lupus erythematosus
- ORPHA:1214Progressive hemifacial atrophy
- ORPHA:1929Rasmussen syndrome
- ORPHA:797Sarcoidosis
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/166484
- This record as JSON: /data/d/166484.json