Rare diseases · Sign or symptom
Abnormal blistering of the skin
Blistering, generalized
HP:0008066
What it means
The presence of one or more bullae on the skin, defined as fluid-filled blisters more than 5 mm in diameter with thin walls.
A bulla is a large vesicle described as a rounded or irregularly shaped blister containing serous or seropurulent fluid, equal to or greater than 10mm. In approaching blistering diseases, there are 3 fundamental criteria to consider: (1) the site or level of the blister (or the lowest level of vesiculation): subcorneal, midepidermis, suprabasal, subepidermal; (2) the findings that implicate the mechanism of blister formation (spongiosis, acantholysis, blistering degeneration, or epidermolysis); and (3) the type of inflammation (neutrophilic, lymphocytic, eosinophilic, mixed), if present.
In everyday care
Most people with this sign do not have a rare disease — it appears in common conditions far more often. These general reference pages cover the same topic:
Rare diseases that can present with this103
Very common80–99%
44- Absence of fingerprints-congenital milia syndrome
- Acrodermatitis enteropathica
- Autosomal dominant epidermolytic ichthyosis
- Autosomal dominant generalized dystrophic epidermolysis bullosa
- Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form
- Autosomal dominant generalized epidermolysis bullosa simplex, severe form
- Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form
- Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form
- Autosomal recessive malignant osteopetrosis
- Bullous diffuse cutaneous mastocytosis
- Bullous impetigo
- Bullous lichen planus
- Bullous pemphigoid
- Congenital erythropoietic porphyria
- Dermatitis herpetiformis
- Dracunculiasis
- Dyskeratosis congenita
- Dystrophic epidermolysis bullosa pruriginosa
- Epidermolysis bullosa acquisita
- Epidermolysis bullosa simplex with anodontia/hypodontia
- Epidermolysis bullosa simplex with mottled pigmentation
- Erythrokeratodermia variabilis
- Focal facial dermal dysplasia type IV
- Hepatoerythropoietic porphyria
- Hereditary acrokeratotic poikiloderma
- IgA pemphigus
- Intermediate generalized junctional epidermolysis bullosa
- Junctional epidermolysis bullosa inversa
- Junctional epidermolysis bullosa with pyloric atresia
- Kindler epidermolysis bullosa
- Linear IgA dermatosis
- Lipoid proteinosis
- Localized dystrophic epidermolysis bullosa, pretibial form
- Localized epidermolysis bullosa simplex
- Localized junctional epidermolysis bullosa
- Paraneoplastic pemphigus
- Pemphigoid gestationis
- Porphyria cutanea tarda
- Pseudoxanthomatous diffuse cutaneous mastocytosis
- Severe generalized junctional epidermolysis bullosa
- Stevens-Johnson syndrome
- Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum
- Superficial epidermolytic ichthyosis
- Toxic epidermal necrolysis
Common30–79%
30- Acquired purpura fulminans
- Acral peeling skin syndrome
- Autosomal recessive generalized epidermolysis bullosa simplex
- Bazex syndrome
- Behçet disease
- Diffuse cutaneous mastocytosis
- Diffuse palmoplantar keratoderma, Bothnian type
- Epidermolysis bullosa simplex with circinate migratory erythema
- Epidermolysis bullosa simplex with pyloric atresia
- Erythema elevatum diutinum
- Glucagonoma
- Hereditary bullous dystrophy, macular type
- Laryngo-onycho-cutaneous syndrome
- Late-onset junctional epidermolysis bullosa
- Localized dystrophic epidermolysis bullosa, acral form
- Maternal uniparental disomy of chromosome 1 syndrome
- NAD(P)HX dehydratase deficiency
- Paternal uniparental disomy of chromosome 1 syndrome
- Pellagra
- Pemphigus erythematosus
- Pemphigus foliaceus
- Pemphigus vulgaris
- Plague
- PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement
- Recessive dystrophic epidermolysis bullosa inversa
- Rothmund-Thomson syndrome
- Self-improving dystrophic epidermolysis bullosa
- Syringocystadenoma papilliferum
- Variegate porphyria
- Wells syndrome
The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions, and Orphanet separately records 1 disease where this sign is specifically absent. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Blister · Blistering, generalised · Blisters · Skin blisters · Skin bullae
Tracking symptoms like this for someone? Eleplan keeps symptoms, diagnoses, medications and every specialist in one plan.
Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.