SE-ATLAS

Acquired angioedema Rare urticaria Epidermolysis bullosa simplex with anodontia/hypodontia Typical urticaria pigmentosa Nodular urticaria pigmentosa Systemic mastocytosis Plaque-form urticaria pigmentosa Drug reaction with eosinophilia and systemic symptoms Epidermolysis bullosa simplex with mottled pigmentation Smoldering systemic mastocytosis Autosomal dominant generalized epidermolysis bullosa simplex, severe form Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement PLCG2-associated antibody deficiency and immune dysregulation Intermediate generalized junctional epidermolysis bullosa Isolated bone marrow mastocytosis Localized epidermolysis bullosa simplex Severe generalized junctional epidermolysis bullosa Junctional epidermolysis bullosa with pyloric atresia Localized junctional epidermolysis bullosa Late-onset junctional epidermolysis bullosa Junctional epidermolysis bullosa inversa Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form Melkersson-Rosenthal syndrome Localized dystrophic epidermolysis bullosa, pretibial form Muckle-Wells syndrome Dystrophic epidermolysis bullosa Recessive dystrophic epidermolysis bullosa inversa Lymphoadenopathic mastocytosis with eosinophilia Epidermolysis bullosa simplex Self-improving dystrophic epidermolysis bullosa Junctional epidermolysis bullosa Suprabasal epidermolysis bullosa simplex Classic mast cell leukemia Basal epidermolysis bullosa simplex Aleukemic mast cell leukemia Kindler epidermolysis bullosa Ectodermal dysplasia-skin fragility syndrome Localized dystrophic epidermolysis bullosa, acral form Localized dystrophic epidermolysis bullosa, nails only Epidermolysis bullosa simplex with circinate migratory erythema Lethal acantholytic erosive disorder Epidermolysis bullosa simplex with pyloric atresia Hereditary angioedema type 1 Cutaneous mastocytoma Maculopapular cutaneous mastocytosis Hereditary angioedema type 2 Diffuse cutaneous mastocytosis F12-related hereditary angioedema with normal C1Inh Acquired angioedema type 1 Acquired angioedema type 2 Renin-angiotensin-aldosterone system-blocker-induced angioedema Bullous diffuse cutaneous mastocytosis Laryngo-onycho-cutaneous syndrome Cutaneous mastocytosis Mastocytosis Autosomal recessive generalized epidermolysis bullosa simplex Junctional epidermolysis bullosa, non-Herlitz type Epidermolysis bullosa simplex superficialis Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form Centripetalis recessive dystrophic epidermolysis bullosa Pruritic urticarial papules and plaques of pregnancy Pseudoxanthomatous diffuse cutaneous mastocytosis Telangiectasia macularis eruptiva perstans Dystrophic epidermolysis bullosa pruriginosa Indolent systemic mastocytosis Aggressive systemic mastocytosis Extracutaneous mastocytoma Systemic mastocytosis with associated hematologic neoplasm Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Mast cell sarcoma Schnitzler syndrome Mast cell leukemia Non-histaminic angioedema Autosomal dominant generalized dystrophic epidermolysis bullosa Inherited epidermolysis bullosa Epidermolysis bullosa simplex with muscular dystrophy Familial cold urticaria Hereditary angioedema