ORPHA:263676

OBSOLETE: Hereditary epidermolysis bullosa associated with ocular features

inactive · referred to ORPHA:79361Inherited epidermolysis bullosa

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 Inherited epidermolysis bullosa

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	OBSOLETE: Hereditary epidermolysis bullosa associated with ocular features
fr	OBSOLETE : Epidermolyse bulleuse héréditaire avec atteintes oculaires
de	OBSOLET: Epidermolysis bullosa, hereditäre, mit assoziierter Augenstörung
es	OBSOLETO: Epidermólisis ampollosa hereditaria asociada a afectación ocular
it	OBSOLETO: Epidermolisi bollosa ereditaria associata a segni oculari
nl	OBSOLEET: Erfelijke epidermolysis bullosa geassocieerd met oculaire kenmerken
pt	OBSOLETO: Epidermólise bolhosa hereditária associada a características oculares
pl	NIEAKTUALNE: Dziedziczne pecherzowe oddzielanie sie naskórka z towarzyszacymi objawami ocznymi
cs	NEAKTUÁLNÍ: Dědičná epidermolysis bullosa s očními příznaky
uk	Спадковий бульозний епідермоліз, повязаний з особливостями очей
zh	弃用：眼部特征相关遗传性大疱性表皮松解症
tr	Eski adı: Oküler özelliklerle ilişkili kalıtsal epidermolizis bülloza

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/263676
This record as JSON: /data/d/263676.json