ORPHA:98753
OBSOLETE: Autoimmune neurological channelopathy due to an acetylcholine receptor subunits defect
inactive · referred to ORPHA:98750Autoimmune neurological channelopathy
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Autoimmune neurological channelopathy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Autoimmune neurological channelopathy due to an acetylcholine receptor subunits defect | |
| fr | OBSOLETE : Canalopathie neurologique auto-immune associé à un défaut de sous-unité du recepteur à l'acétylcholine | |
| de | OBSOLET: Ionenkanalkrankheit, autoimmune neurologische, bei Defekt einer Untereinheit des Acetylcholin-Rezeptors | |
| es | OBSOLETO: Canalopatía neurológica autoinmune por un defecto de las subunidades del receptor de la acetilcolina | |
| it | OBSOLETO: Canalopatia neurologica autoimmune da difetto delle subunità del recettore acetilcolinico | |
| nl | OBSOLEET: Auto-immune neurologische kanalopathie door een acetylcholinereceptor-subeenhedendefect | |
| pt | OBSOLETO: Canalopatia neurológica autoimune por defeito nas subunidades do recetor da acetilcolina | |
| pl | NIEAKTUALNE: Autoimmunologiczna kanalopatia neurologiczna z powodu defektu podjednostki receptora dla acetylocholiny | |
| cs | NEAKTUÁLNÍ: Autoimunitní kanálopatie způsobené poruchou podjednotek receptoru pro acetylcholin | |
| uk | ЗАСТАРІЛО: Аутоімунна неврологічна каналопатія, спричинена дефектом субодиниць ацетилхолінових рецепторів | |
| zh | 乙酰胆碱受体亚基缺陷所致自身免疫性神经离子通道病 | |
| tr | Eski adı: Bir asetilkolin reseptör alt birim defektine bağlı otoimmün nörolojik kanalopati |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
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/98753
- This record as JSON: /data/d/98753.json