ORPHA:98124
OBSOLETE: Channelopathy due to a skeletal muscle acetylcholine receptor defect
inactive · referred to ORPHA:590Congenital myasthenic syndrome
- 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 Congenital myasthenic syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Channelopathy due to a skeletal muscle acetylcholine receptor defect | |
| fr | OBSOLETE : Canalopathie associée à un défaut du recepteur musculaire à l'acétylcholine | |
| de | OBSOLET: Ionenkanalkrankheit bei skeletomuskulärem ACh-Rezeptordefekt | |
| es | OBSOLETO: Canalopatía por un defecto del receptor de acetilcolina del músculo esquelético | |
| it | OBSOLETO: Canalopatia da difetti del recettore Ach nel muscolo scheletrico | |
| nl | OBSOLEET: Kanalopathie als gevolg van een skeletspier acetylcholinereceptordefect | |
| pt | OBSOLETO: Canalopatia por defeito do recetor da acetilcolina do músculo esquelético | |
| pl | NIEAKTUALNE: Kanalopatia z powodu defektu receptora acetylocholiny w miesniach szkieletowych | |
| cs | NEAKTUÁLNÍ: Kanalopatie způsobená poruchou acetylcholinových receptorů kosterních svalů | |
| uk | ЗАСТАРІЛО: Каналопатія внаслідок дефекту ацетилхолінових рецепторів скелетних мязів | |
| zh | 弃用：骨骼肌乙酰胆碱受体缺陷离子通道病 | |
| tr | Eski adı: İskelet kası asetilkolin reseptör defektine bağlı 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/98124
- This record as JSON: /data/d/98124.json