raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:158665

OBSOLETE: Basal epidermolysis bullosa simplex

inactive · referred to ORPHA:304Epidermolysis bullosa simplex

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 Epidermolysis bullosa simplex

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enOBSOLETE: Basal epidermolysis bullosa simplex
frOBSOLETE : Epidermolyse bulleuse simple basale
deOBSOLET: Epidermolysis bullosa simplex, basale
esOBSOLETO: Epidermólisis ampollosa simple basalOBSOLETO: Epidermólisis bullosa simple basal
itOBSOLETO: Epidermolisi bollosa semplice basale
nlOBSOLEET: Basale epidermolysis bullosa simplex
ptOBSOLETO: Epidermólise bolhosa simples basal
plNIEAKTUALNE: Postać prosta pęcherzowego oddzielania się naskórka
csNEAKTUÁLNÍ: Bazální epidermolysis bullosa simplex
ukЗАСТАРІЛО: Простий базальний бульозний епідермоліз
zh基底层单纯性大疱性表皮松解症
trBazal epidermolizis bülloza simpleks
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