ORPHA:98122

OBSOLETE: Channelopathy due to a neuronal glycine receptor defect

inactive · referred to ORPHA:3197Hereditary hyperekplexia

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 Hereditary hyperekplexia

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Channelopathy due to a neuronal glycine receptor defect
fr	OBSOLETE : Canalopathie associée à un défaut du recepteur neuronal de la glycine
de	OBSOLET: Ionenkanalkrankheit bei neuronalem Glycin-Rezeptordefekt
es	OBSOLETO: Canalopatía por un defecto del receptor de glicina neuronal
it	OBSOLETO: Canalopatia da difetti del recettore neuronale della glicina
nl	OBSOLEET: Kanalopathie als gevolg van een neuronaal glycinereceptordefect
pt	OBSOLETO: Canalopatia por defeito do recetor neuronal da glicina
pl	NIEAKTUALNE: Kanalopatia z powodu defektu neuronalnego receptora glicynowego
cs	NEAKTUÁLNÍ: Kanalopatie způsobená poruchou neuronálních glycinových receptorů
uk	ЗАСТАРІЛО: Каналопатія внаслідок дефекту гліцинових рецепторів нейронів
zh	弃用：神经元甘氨酸受体缺陷离子通道病
tr	Eski adı: Nöronal glisin reseptör defektine bağlı kanal gelişimi

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/98122
This record as JSON: /data/d/98122.json