SE-ATLAS

Acquired angioedema Acquired angioedema type 1 Acquired angioedema type 2 Aggressive systemic mastocytosis Aleukemic mast cell leukemia 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 Bullous diffuse cutaneous mastocytosis Centripetalis recessive dystrophic epidermolysis bullosa Classic mast cell leukemia Cutaneous mastocytoma Cutaneous mastocytosis Diffuse cutaneous mastocytosis Drug reaction with eosinophilia and systemic symptoms Dystrophic epidermolysis bullosa Dystrophic epidermolysis bullosa pruriginosa Ectodermal dysplasia-skin fragility syndrome 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 Extracutaneous mastocytoma F12-related hereditary angioedema with normal C1Inh Familial cold urticaria Hereditary angioedema Hereditary angioedema type 1 Hereditary angioedema type 2 Indolent systemic mastocytosis Inherited epidermolysis bullosa Intermediate generalized junctional epidermolysis bullosa Isolated bone marrow mastocytosis Junctional epidermolysis bullosa Junctional epidermolysis bullosa inversa Junctional epidermolysis bullosa with pyloric atresia Junctional epidermolysis bullosa, non-Herlitz type 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 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 Lymphoadenopathic mastocytosis with eosinophilia Maculopapular cutaneous mastocytosis Mast cell leukemia Mast cell sarcoma Mastocytosis Melkersson-Rosenthal syndrome Muckle-Wells syndrome Nodular urticaria pigmentosa Non-histaminic angioedema PLCG2-associated antibody deficiency and immune dysregulation PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement Plaque-form urticaria pigmentosa Pruritic urticarial papules and plaques of pregnancy Pseudoxanthomatous diffuse cutaneous mastocytosis Rare urticaria Recessive dystrophic epidermolysis bullosa inversa Renin-angiotensin-aldosterone system-blocker-induced angioedema Schnitzler syndrome Self-improving dystrophic epidermolysis bullosa Severe generalized junctional epidermolysis bullosa Smoldering systemic mastocytosis Suprabasal epidermolysis bullosa simplex Systemic mastocytosis Systemic mastocytosis with associated hematologic neoplasm Telangiectasia macularis eruptiva perstans Typical urticaria pigmentosa