raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:98114

OBSOLETE: Non-pore-loop channelopathy due to epithelial Cl- channel bestrophin anomaly

inactive · referred to ORPHA:1243Best vitelliform macular dystrophy

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 Best vitelliform macular dystrophy

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Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Non-pore-loop channelopathy due to epithelial Cl- channel bestrophin anomaly
frOBSOLETE : 'Canalopathie non ''pore loop'' due à un défaut du canal chlorure épithélial bestrophine'
deOBSOLET: Ionenkanalkrankheit bei epithelialem Bestrophin/Chloridikanaldefekt
esOBSOLETO: Canalopatía 'non-pore-loop' por una anomalía del canal de Cl- epitelial bestrofina
itOBSOLETO: Canalopatia da difetti del canale epiteliale del cloro bestrofina
nlOBSOLEET: Non-pore-loop-kanalopathie als gevolg van epitheliaal Cl-kanaalbestrofineanomalie
ptOBSOLETO: Canalopatia não-''pore-loop'' por anomalia do canal de cloro epitelial bestrofina
plNIEAKTUALNE: Defekt kanalów nie posiadajacych petli z powodu anomalii nablonkowego kanalu chlorkowego bestrofiny
csNEAKTUÁLNÍ: Non-pore-loop kanalopatie způsobená bestrofinovou anomálií Cl- epiteliálních kanálů
ukЗАСТАРІЛО: Каналопатія без порової петлі, зумовлена епітеліальною аномалією бестрофіну Cl-каналів.
zh弃用:上皮细胞氯离子通道斑萎蛋白异常所致非孔-环离子通道病
trEski adı: Epitelyal Cl- kanal bestrofin anomalisine bağlı gözeneksiz kanal kanalopati
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Cross-references

qualifier = Orphanet mapping relation

No 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 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

0 records

No 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