Incoming and outgoing links Epidermolysis bullosa hereditaria (overview)
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Outgoing links
- Acral peeling skin syndrome
- Acrodermatitis enteropathica
- Antibiogram
- Antibiotics
- Aplasia cutis congenita (overview)
- Basal membrane
- Bullous Pemphigoid
- Candidoses
- COL7A1 Gene
- Contagious impetigo
- Cytoskeleton
- Dermatitis herpetiformis
- Desmosomes
- DSP Gene
- DST Gene
- Dystrophic epidermolysis bullosa inversa
- Dystrophic epidermolysis bullosa pruriginosa recessive
- Ectodermal dysplasia-skin fragility syndrome
- Ema
- Epidermolysis bullosa acquisita
- Epidermolysis bullosa dystrophica albopapuloida
- Epidermolysis bullosa dystrophica dominans, generalized
- Epidermolysis bullosa dystrophica praetibialis
- Epidermolysis bullosa dystrophica recessive non-hallopeau-siemens
- Epidermolysis bullosa dystrophica recessive, severe generalized
- Epidermolysis bullosa junctionalis generalized intermediaries (non-herlitz)
- Epidermolysis bullosa junctionalis, generalized severe (historical: Herlitz type)
- Epidermolysis bullosa junctionalis with hypacusis
- Epidermolysis bullosa junctionalis with pyloric atresia
- Epidermolysis bullosa, lethal acantholytic
- Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive
- Epidermolysis bullosa simplex 3, basal, autosomal recessive, with bp230 deficiency
- Epidermolysis Bullosa Simplex 3, Localized or Generalized Intermediate, with Bp230 Deficiency (EBS3)
- Epidermolysis bullosa simplex generalized intermediaries (köbner)
- Epidermolysis bullosa simplex generalized severe (dowling-meara)
- Epidermolysis bullosa simplex, localized or generalized intermediate, with mutation in EXPH5
- Epidermolysis bullosa simplex localized (Weber-Cockayne)
- Epidermolysis bullosa simplex mit Mutation in Plectin-Isoform 1a
- Epidermolysis bullosa simplex "ogna
- Epidermolysis Bullosa Simplex with KLHL24 Mutations
- Epidermolysis bullosa simplex with mottled pigmentation
- Epidermolysis bullosa simplex with muscular dystrophy an mutation in PLEC
- Epidermolysis bullosa simplex with pyloric atresia and mutation in PLEC
- Epidermolysis bullosa with congenital abscence of the skin and deformity of nails
- EXPH5 Gene
- Glucorticosteroids topical
- Herpes simplex virus infections
- Interstitial lung disease , nephrotic syndrome and integrin alpha-3 Mutation
- Isolated toenail dystrophy
- ITGB4 Gene
- Kindler syndrome
- KLHL24 Gene
- KRT14 Gene
- KRT5 Gene
- LAMA3 Gene
- Laryngo-onycho-cutaneous-syndrome
- Linear IgA dermatosis
- Mastocytosis (overview)
- Orphan diseases
- Peeling skin syndrome
- Pemphigus diseases (overview)
- Pigment incontinence
- PKP1 Gene
- PLEC Gene
- Polihexanide
- Porphyria (overview)
- Potassium permanganate
- Pretibial dystrophic epidermolysis bullosa, recessive
- Pruritus
- Skin fragility-woolly hair syndrome
- Staphylococcal scalded skin syndrome
- TGM5 Gene
- Thymic stromal lymphopoietin
- Transient bullous dermolysis of the newborn
- Triamcinolone acetonide
- Urea (overview)
- Wound treatment
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