SE-ATLAS

Ectodermal dysplasia syndrome Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency T-B+ severe combined immunodeficiency due to gamma chain deficiency Severe combined immunodeficiency due to adenosine deaminase deficiency 22q11.2 deletion syndrome Hyper-IgM syndrome type 2 Angioosteohypertrophic syndrome Muckle-Wells syndrome Chédiak-Higashi syndrome Omenn syndrome Autosomal erythropoietic protoporphyria Cartilage-hair hypoplasia Angiosarcoma X-linked agammaglobulinemia Amylose cutanée primitive Syndrome de Hermansky-Pudlak Syndrome de Cockayne Syndrome de Sturge-Weber Syndrome du naevus épidermique Adénolipomatose symétrique à prédominance cervicale Trichothiodystrophie Xeroderma pigmentosum Neutropénie cyclique Syndrome de Griscelli type 2 Déficit d'adhésion leucocytaire Granulomatose chronique