ORPHA:98751
OBSOLETE: Autoimmune neurological channelopathy due to a p/q-type voltage gated calcium channel 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 a p/q-type voltage gated calcium channel defect | |
| fr | OBSOLETE : Canalopathie neurologique auto-immune associée au canal calcique volyage dépendant de type p/q | |
| de | OBSOLET: Ionenkanalkrankheit, autoimmune neurologische, bei Defekt des p/q-Typ spannungsabhängigen Kalziumkanals | |
| es | OBSOLETO: Canalopatía neurológica autoinmune por un defecto del canal de calcio dependiente de voltaje tipo p/q | |
| it | OBSOLETO: Canalopatia neurologica autoimmune da difetto del canale del calcio voltaggio-dipendente, tipo p/q | |
| nl | OBSOLEET: Auto-immune neurologische kanalopathie door een p/q-type spanning-gated calciumkanaaldefect | |
| pt | OBSOLETO: Canalopatia neurológica autoimune por anomalia dos canais de cálcio dependentes de voltagem tipo p/q | |
| pl | NIEAKTUALNE: Autoimmunologiczna kanalopatia neurologiczna z powodu defektu napieciowo-zaleznego kanalu wapniowego typu p/q | |
| cs | NEAKTUÁLNÍ: Autoimunitní kanálopatie způsobené poruchou p/q-typu napěťově řízeného kanálu pro vápník | |
| uk | ЗАСТАРІЛО: Аутоімунна неврологічна каналопатія внаслідок дефекту потенціалкерованих кальцієвих каналів p/q типу | |
| zh | P/Q型电压门控钙通道缺陷所致自身免疫性神经离子通道病 | |
| tr | Eski adı: p / q tipi voltaj kapılı kalsiyum kanal 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/98751
- This record as JSON: /data/d/98751.json