Klinik für Dermatologie und Venerologie am Universitätsklinikum Freiburg Assigned diseases:
In the following you will find the diseases that are treated in this facility:
Autoerythrocyte sensitization syndrome
Autoimmune bullous skin disease
Autoimmune disease with skin involvement
Autoinflammatory syndrome with skin involvement
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 generalized epidermolysis bullosa simplex
Basal epidermolysis bullosa simplex
Benign cephalic histiocytosis
Bockenheimer syndrome
Bullous pemphigoid
CREST syndrome
Calciphylaxis cutis
Centripetalis recessive dystrophic epidermolysis bullosa
Chilblain lupus
Chronic cutaneous lupus erythematosus
Cutaneous collagenous vasculopathy
Dermatitis herpetiformis
Diffuse cutaneous systemic sclerosis
Discoid lupus erythematosus
Drug-induced lupus erythematosus
Dystrophic epidermolysis bullosa
Dystrophic epidermolysis bullosa pruriginosa
Ectodermal dysplasia-skin fragility syndrome
Epidermolysis bullosa acquisita
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex superficialis
Epidermolysis bullosa simplex with anodontia/hypodontia
Epidermolysis bullosa simplex with circinate migratory erythema
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolysis bullosa simplex with pyloric atresia
Erdheim-Chester disease
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome
Familial multiple nevi flammei
Generalized eruptive histiocytosis
Generalized essential telangiectasia
Generalized pustular psoriasis
Hereditary progressive mucinous histiocytosis
Herpetiform pemphigus
Hypertrophic or verrucous lupus erythematosus
Indeterminate cell histiocytosis
Infantile onset panniculitis with uveitis and systemic granulomatosis
Inherited epidermolysis bullosa
Intermediate generalized junctional epidermolysis bullosa
Junctional epidermolysis bullosa
Junctional epidermolysis bullosa inversa
Junctional epidermolysis bullosa with pyloric atresia
Junctional epidermolysis bullosa, non-Herlitz type
Juvenile xanthogranuloma
Kindler epidermolysis bullosa
Laryngo-onycho-cutaneous syndrome
Late-onset junctional epidermolysis bullosa
Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
Lethal acantholytic erosive disorder
Limited cutaneous systemic sclerosis
Limited systemic sclerosis
Linear IgA dermatosis
Localized dystrophic epidermolysis bullosa, acral form
Localized dystrophic epidermolysis bullosa, nails only
Localized dystrophic epidermolysis bullosa, pretibial form
Localized epidermolysis bullosa simplex
Localized junctional epidermolysis bullosa
Localized scleroderma
Lupus erythematosus panniculitis
Lupus erythematosus tumidus
Mucous membrane pemphigoid
Multicentric reticulohistiocytosis
Necrobiotic xanthogranuloma
Non-Langerhans cell histiocytosis
PAPA syndrome
PASH syndrome
PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement
Papular xanthoma
Paraneoplastic pemphigus
Pemphigoid gestationis
Pemphigus erythematosus
Pemphigus foliaceus
Pemphigus vegetans
Pemphigus vulgaris
Progressive nodular histiocytosis
Rare cutaneous lupus erythematosus
Recessive dystrophic epidermolysis bullosa inversa
Reynolds syndrome
Scleroderma
Self-improving dystrophic epidermolysis bullosa
Severe generalized junctional epidermolysis bullosa
Skin vascular disease
Subacute cutaneous lupus erythematosus
Superficial pemphigus
Suprabasal epidermolysis bullosa simplex
Systemic disease with skin involvement
Systemic sclerosis
Xanthoma disseminatum