ORPHA:255117

OBSOLETE: Autosomal dominant optic atrophy and late-onset deafness

inactive · referred to ORPHA:1215Autosomal dominant optic atrophy plus syndrome

Type: Disease
Group: Disorder
Status: inactive
Flag: Obsolete entity

This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Autosomal dominant optic atrophy plus syndrome

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Autosomal dominant optic atrophy and late-onset deafness
fr	OBSOLETE : Atrophie optique autosomique dominante et surdité tardive
de	OBSOLET: Optikusatrophie, autosomal-dominante, mit spät-einsetzender Schwerhörigkeit
es	OBSOLETO: Atrofia óptica autosómica dominante y sordera de inicio tardío
it	OBSOLETO: Atrofia ottica autosomica dominante e sordità a esordio tardivo
nl	OBSOLEET: Autosomaal dominante opticusatrofie en doofheid met late aanvang	OBSOLEET: Autosomaal dominante optische atrofie en doofheid met late aanvang
pt	OBSOLETO: Atrofia óptica autossómica dominante e surdez de início tardio
pl	NIEAKTUALNE: Autosomalny dominujacy zanik nerwu wzrokowego i gluchota o póznym poczatku
cs	NEAKTUÁLNÍ: Autozomálně dominantní atrofie optiku a pozdní hluchota
uk	ЗАСТАРІЛО: Аутосомно-домінантна атрофія зорового нерва та пізня глухота
zh	弃用：常染色体显性遗传性视神经萎缩和迟发性耳聋
tr	Eski adı: Otozomal dominant optik atrofi ve geç başlangıçlı sağırlık

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/255117
This record as JSON: /data/d/255117.json