SE-ATLAS

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