raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:89839

OBSOLETE: Epidermolysis bullosa simplex superficialis

inactive · referred to ORPHA:304Epidermolysis bullosa simplex

Synonyms: OBSOLETE: EBSS

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 Epidermolysis bullosa simplex

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Epidermolysis bullosa simplex superficialisOBSOLETE: EBSS
frOBSOLETE : Epidermolyse bulleuse simple superficielleOBSOLETE : EBSS
deOBSOLET: Epidermolysis bullosa simplex superficialisOBSOLET: EBSS
esOBSOLETO: Epidermólisis ampollosa simple superficialOBSOLETO: EAS superficial · OBSOLETO: Epidermólisis bullosa simple superficial
itOBSOLETO: Epidermolisi bollosa semplice superficialeOBSOLETO: EBSS
nlOBSOLEET: Epidermolysis bullosa simplex superficialisOBSOLEET: EBSS
ptOBSOLETO: Epidermólise bolhosa simples superficialOBSOLETO: EBSS
plNIEAKTUALNE: Pęcherzowe oddzielanie się naskórka, postać prosta powierzchowna= en
csNEAKTUÁLNÍ: Epidermolysis bullosa simplex superficialisNEAKTUÁLNÍ: EBSS
ukЗАСТАРІЛО: Простий поверхневий бульозний епідермолізЗАСТАРІЛО: EBSS
zh浅表型单纯型大疱性表皮松解症EBSS
trEpidermolizis bülloza simpleks süperfisiyalisEBSS
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

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

7

Sources for this card