epidermolysis bullosa acquisita
MeSH: D016107ORPHA: 46487
Overview
chronic subepidermal blistering disease associated with autoimmunity to type VII collagen
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with epidermolysis bullosa acquisita, sourced from HPO and Orphanet clinical annotations.
Diabetes mellitusHyperpigmentation of the skinAtypical scarring of skinPruritusMiliaAbnormal hair morphologyAbdominal painInflammation of the large intestineAbnormal blistering of the skinNail dystrophy
Classification & Codes
MeSH Code
D016107Orphanet Code
ORPHA:46487epidermolysis bullosa acquisita
| MeSH | D016107 |
| Orphanet | ORPHA:46487 |
| Treatments | 0 drug(s) |
| Symptoms on record | 10 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO