raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:79669

Autoimmune bullous skin disease

Type
Clinical group
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAutoimmune bullous skin disease
frDermatite bulleuse auto-immune
deHautkrankheit, autoimmune bullöse
esEnfermedad de la piel ampollosa autoinmune
itMalattia autoimmune bollosa cutanea
nlAuto-immune bulleuze huidziekte
ptDoença cutânea bolhosa autoimune
plAutoimmunologiczna pęcherzowa choroba skóry
csAutoimunitní bulózní kožní onemocnění
ukАутоімунне бульозне захворювання шкіри
zh自身免疫性大疱性皮肤病
trOtoimmün büllöz deri hastalığı
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0019337Evalidated
MONDO19337Evalidated
UMLSC5681494Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (12):

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