SE-ATLAS

Mapping of Health Care Providers
for People with Rare 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