SE-ATLAS

Primary ciliary dyskinesia Juvenile dermatomyositis Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis Immunodeficiency due to CD25 deficiency Immunodeficiency due to a complement cascade protein anomaly Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency LIG4 syndrome Primary ciliary dyskinesia-retinitis pigmentosa syndrome NLRP3-associated autoinflammatory disease Barth syndrome JMP syndrome Chronic pneumonitis of infancy Secondary interstitial lung disease specific to childhood associated with a granulomatous disease Ataxia-telangiectasia-like disorder Primary immunodeficiency PAPA syndrome Sarcoidosis Exposure-related interstitial lung disease Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency Tuberculosis Secondary interstitial lung disease specific to childhood associated with a metabolic disease X-linked immunoneurologic disorder Yellow nail syndrome Combined immunodeficiency due to IL21R deficiency Pediatric Castleman disease Short-limb skeletal dysplasia with severe combined immunodeficiency Diffuse panbronchiolitis Behçet disease Combined immunodeficiency due to DOCK8 deficiency Complement component 3 deficiency Non-specific interstitial pneumonia Asbestos intoxication Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency Anti-neutrophil cytoplasmic antibody-associated vasculitis Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency Idiopathic pulmonary fibrosis Pediatric systemic lupus erythematosus X-linked lymphoproliferative disease CANDLE syndrome Immunoglobulin heavy chain deficiency Autoimmune lymphoproliferative syndrome Giant cell arteritis Genetic susceptibility to infections due to particular pathogens Bloom syndrome Familial cold urticaria Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency Severe combined immunodeficiency due to LCK deficiency Mixed connective tissue disease Neutrophil immunodeficiency syndrome Langerhans cell histiocytosis specific to childhood Osteopetrosis-hypogammaglobulinemia syndrome Vici syndrome Lymphangioleiomyomatosis Shwachman-Diamond syndrome Familial hemophagocytic lymphohistiocytosis Say-Barber-Miller syndrome Bacterial susceptibility due to TLR signaling pathway deficiency Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency Hypocomplementemic urticarial vasculitis Papillon-Lefèvre syndrome Myeloperoxidase deficiency Chronic beryllium disease Brain-lung-thyroid syndrome Interstitial lung disease specific to adulthood Facial dysmorphism-immunodeficiency-livedo-short stature syndrome Susceptibility to viral and mycobacterial infections due to STAT1 deficiency CREST syndrome Hajdu-Cheney syndrome T-cell immunodeficiency with thymic aplasia Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Primary interstitial lung disease specific to adulthood Dyskeratosis congenita Severe acute respiratory syndrome Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency Severe combined immunodeficiency due to DCLRE1C deficiency T-B+ severe combined immunodeficiency due to gamma chain deficiency Primary immunodeficiency syndrome due to LAMTOR2 deficiency Severe combined immunodeficiency due to adenosine deaminase deficiency Juvenile polymyositis Apnea of prematurity Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency Combined immunodeficiency with granulomatosis Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome Dianzani autoimmune lymphoproliferative disease Pulmonary interstitial glycogenosis Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome Sudden infant death-dysgenesis of the testes syndrome Interstitial lung disease Syndrome lymphoprolifératif auto-immun avec infections virales récurrentes Maladie de Kawasaki Asplénie congénitale familiale isolée Microlithiase pulmonaire alvéolaire Pneumopathie interstitielle secondaire spécifique de l'adulte associée à une maladie systémique Artérite de Takayasu Hyperzincémie et hypercalprotectinémie Pneumoconiose Hyperplasie lymphoïde nodulaire pulmonaire Neutropénie congénitale sévère autosomique récessive par déficit en G6PC3 Hyperplasie des cellules neuroendocrines du nourrisson Infection récurrente par déficit en granules spécifiques Hypoglammaglobulinémie transitoire de l'enfance Arthrite juvénile idiopathique oligoarticulaire avec anticorps anti-noyaux Syndrome de maladie veino-occlusive hépatique-déficit immunitaire Vascularite post-infectieuse Syndrome de Pearson Histiocytose langerhansienne spécifique de l'adulte Pneumopathie interstitielle aiguë Syndrome de PI3K-delta activé Pneumopathie interstitielle de l'enfance et de l'adulte Détresse respiratoire chronique avec déficit du métabolisme du surfactant Pneumopathie interstitielle secondaire de l'enfant et de l'adulte associée à une maladie du tissu conjonctif Papillomatose respiratoire récurrente Arthrite réactionnelle Immunodéficence due à un déficit des composés classiques de la voie classique du complément Bronchiectasie idiopathique Pneumopathie interstitielle lymphocytaire Détresse respiratoire aiguë néonatale par déficit en SP-B Prédisposition mendélienne autosomique dominante aux infections mycobactériennes par déficit partiel en IFNgammaR1 Encéphalite à herpes simplex Pneumonie à éosinophiles idiopathique Bronchiolite respiratoire avec pneumopathie interstitielle Syndrome auto-inflammatoire de l'enfant Syndrome de délétion 22q11.2 Déficit immunitaire combiné par déficit en CARD11 Déficit immunitaire par déficit des composés terminaux de la voie classique du complément Déficit immunitaire par déficit en MASP-2 Prédisposition mendélienne aux infections mycobactériennes par déficit partiel en STAT1 Arthrite juvénile idiopathique oligoarticulaire sans anticorps anti-noyaux Déficit immunitaire combiné sévère T-B+ par déficit en JAK3 Déficit immunitaire combiné sévère T-B+ par déficit en IL-7Ralpha Déficit immunitaire par déficit d'expression des molécules CMH de classe II Syndrome de Nijmegen-like Fasciite à éosinophiles Arthrite juvénile idiopathique polyarticulaire sans facteur rhumatoïde Prédisposition mendélienne autosomique dominante aux infections mycobactériennes par déficit partiel en IFNgammaR2 Epidermodysplasie verruciforme Syndrome de Muckle-Wells Syndrome de Siegler-Brewer-Carey Dérèglement et déficit immunitaire lié à PLCG2 Neutropénie constitutionnelle avec manifestations extra-hématopoïétiques Vascularite cryoglobulinémique Arthrite juvénile idiopathique oligoarticulaire Syndrome de Chédiak-Higashi Agammaglobulinémie isolée Pneumopathie interstitielle primaire de l'enfance et de l'adulte Prédisposition mendélienne aux infections mycobactériennes par déficit partiel en IRF8 Déficit immunitaire combiné sévère T-B- Autre syndrome de déficit immunitaire par défaut de l'immunité innée Arthrite juvénile idiopathique indéterminée Syndrome d'Omenn Arthrite juvénile idiopathique systémique Déficit immunitaire combiné sévère T-B+ par déficit en CD45 Arthrite juvénile idiopathique sans facteur rhumatoïde avec anticorps anti-nucléaire Arthrite juvénile idiopathique sans facteur rhumatoïde sans anticorps anti-nucléaire Déficit immunitaire par déficit en ficoline 3 Agammaglobulinémie syndromique Déficit immunitaire combiné sévère T-B+ Syndrome de pneumopathie interstitielle-syndrome néphrotique-épidermolyse bulleuse Déficit immunitaire combiné sévère T-B+ par déficit en CD3delta/epsilon/zêta Déficit immunitaire combiné par déficit en STK4 Pneumothorax spontané familial Chondrodysplasie métaphysaire autosomique récessive Syndrome de Roifman Mucoviscidose Syndrome d'entéropathie et endocrinopathie auto-immunes-susceptibilité aux infections chroniques Arthrite juvénile idiopathique polyarticulaire Déficit immunitaire combiné par déficit en ORAI1 Neutropénie sévère congénitale liée à l'X Déficit immunitaire combiné par déficit en STIM1 Hémorragie alvéolaire diffuse Polyendocrinopathie auto-immune type 1 Syndrome de fièvre récurrente héréditaire Polyangéite microscopique Prédisposition mendélienne liée à l'X aux infections mycobactériennes Syndrome de Kostmann Syndrome de fièvre périodique héréditaire lié à NLRP12 Polychondrite atrophiante Granulomatose éosinophilique avec polyangéite Neutropénie congénitale sévère Déficit immunitaire combiné sévère par déficit en DNA-PKcs Agammaglobulinémie liée à l'X Déficit en anticorps spécifiques avec une quantité normale d'immunoglobuline et de cellules B Syndrome de Blau Syndrome auto-inflammatoire avec déficit immunitaire Syndrome de Hoyeraal-Hreidarsson Déficit immunitaire combiné avec anomalies faciooculosquelettiques Syndrome de fièvre récurrente de l'enfant Syndrome d'insuffisance antéhypophysaire-déficit immunitaire variable Syndrome auto-inflammatoire-dérèglement avec déficit immunitaire lié à PLCG2 Déficit immunitaire combiné sévère par déficit complet en RAG1/2 Syndrome mixte auto-inflammatoire et auto-immun Arthrite juvénile idiopathique polyarticulaire avec facteur rhumatoïde Arthrite juvénile idiopathique associée au psoriasis Déficit immunitaire associé à une anomalie du facteur I Syndrome de Cohen Dysplasie immuno-osseuse de Schimke Déficit immunitaire par absence de thymus Arthrite juvénile idiopathique associée aux enthésopathies Pneumopathie interstitielle primaire de l'enfant et de l'adulte due à une anomalie de la structure alvéolaire Prédisposition mendélienne aux infections mycobactériennes par déficit complet en IFNgammaR1 Agression pulmonaire aiguë Pneumopathie interstitielle spécifique de l'enfance Alpha-1-antitrypsin deficiency Laron syndrome with immunodeficiency 16q24.1 microdeletion syndrome Young syndrome Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder Pyogenic autoinflammatory syndrome of childhood Rare systemic or rheumatological disease of childhood Adult acute respiratory distress syndrome Syndrome with combined immunodeficiency Primary immunodeficiency due to a defect in adaptive immunity Immunodeficiency with factor H anomaly Autoimmune pulmonary alveolar proteinosis Unclassified autoinflammatory syndrome of childhood Mendelian susceptibility to mycobacterial diseases Hypohidrotic ectodermal dysplasia with immunodeficiency House allergic alveolitis Primary interstitial lung disease specific to childhood Farmer's lung disease Occupational allergic alveolitis Familial Mediterranean fever Sterile multifocal osteomyelitis with periostitis and pustulosis Hyper-IgE syndrome Secondary interstitial lung disease in childhood and adulthood Pigeon-breeder lung disease Infantile onset panniculitis with uveitis and systemic granulomatosis Granulomatous autoinflammatory syndrome of childhood Primary interstitial lung disease specific to childhood due to alveolar structure disorder Recurrent Neisseria infections due to factor D deficiency Lichtenstein syndrome Infant acute respiratory distress syndrome Common variable immunodeficiency Allergic bronchopulmonary aspergillosis Gorham-Stout disease Susceptibility to infection due to TYK2 deficiency Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease Cryptogenic organizing pneumonia Severe combined immunodeficiency FADD-related immunodeficiency Hereditary pulmonary alveolar proteinosis Tracheobronchopathia osteochondroplastica Meconium aspiration syndrome Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Bronchiolitis obliterans Idiopathic recurrent pericarditis Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Reticular dysgenesis Autosomal dominant severe congenital neutropenia Infantile apnea Immunodeficiency due to selective anti-polysaccharide antibody deficiency Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells Hyper-IgM syndrome with susceptibility to opportunistic infections Purine nucleoside phosphorylase deficiency Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency Immunoglobulin A vasculitis Overlapping connective tissue disease Unexplained periodic fever syndrome of childhood WHIM syndrome Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome Congenital alveolar capillary dysplasia Selective IgM deficiency Granulomatosis with polyangiitis Spondyloenchondrodysplasia Other immunodeficiency syndrome with predominantly antibody defects DNA repair defect other than combined T-cell and B-cell immunodeficiencies Primary interstitial lung disease specific to childhood due to alveolar vascular disorder Langerhans cell histiocytosis in childhood and adulthood Rare pediatric systemic disease Hyper-IgM syndrome without susceptibility to opportunistic infections Immunodeficiency by defective expression of MHC class I ICF syndrome Idiopathic juvenile osteoporosis Combined T and B cell immunodeficiency Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells Idiopathic CD4 lymphocytopenia CINCA syndrome Congenital chylothorax Absent thumb-short stature-immunodeficiency syndrome PFAPA syndrome Wiskott-Aldrich syndrome Cernunnos-XLF deficiency Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome Rare pediatric vasculitis Agammaglobulinemia Tumor necrosis factor receptor 1 associated periodic syndrome Immuno-osseous dysplasia Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome Combined immunodeficiency due to CD3gamma deficiency Secondary pulmonary hemosiderosis Juvenile idiopathic arthritis Immunodeficiency syndrome with autoimmunity Combined immunodeficiency due to CD27 deficiency Severe combined immunodeficiency due to CORO1A deficiency Congenital neutropenia-myelofibrosis-nephromegaly syndrome Drug-induced vasculitis Isolated pulmonary capillaritis Combined immunodeficiency due to ZAP70 deficiency Poikiloderma with neutropenia Staphylococcal necrotizing pneumonia Recurrent infections associated with rare immunoglobulin isotypes deficiency Idiopathic pulmonary hemosiderosis Congenital diaphragmatic hernia Cyclic neutropenia Primary hemophagocytic lymphohistiocytosis Immunodeficiency predominantly affecting antibody production Lymphoproliferative syndrome Immunodeficiency syndrome with hypopigmentation T-cell immunodeficiency with epidermodysplasia verruciformis Congenital pulmonary lymphangiectasia Functional neutrophil defect Pancytopenia due to IKZF1 mutations Hypersensitivity pneumonitis Proteasome-associated autoinflammatory syndrome Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease Idiopathic interstitial pneumonia Unclassified vasculitis X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia Neutropenia-monocytopenia-deafness syndrome Interstitial lung disease specific to infancy Combined pulmonary fibrosis-emphysema syndrome Combined immunodeficiency due to CRAC channel dysfunction Susceptibility to respiratory infections associated with CD8alpha chain mutation Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Ataxia-telangiectasia Majeed syndrome Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis Constitutional neutropenia Nijmegen breakage syndrome Secondary interstitial lung disease specific to childhood associated with a systemic disease Properdin deficiency Unexplained long-lasting fever/inflammatory syndrome Anti-glomerular basement membrane disease Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency Cogan syndrome Combined immunodeficiency due to partial RAG1 deficiency Leukocyte adhesion deficiency Syndromic multisystem autoimmune disease due to Itch deficiency Autosomal agammaglobulinemia Desquamative interstitial pneumonia Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency Drug or radiation exposure-related interstitial lung disease Primary immunodeficiency due to a defect in innate immunity Severe dermatitis-multiple allergies-metabolic wasting syndrome Severe combined immunodeficiency due to FOXN1 deficiency RAS-associated autoimmune leukoproliferative disease Secondary interstitial lung disease specific to childhood associated with a connective tissue disease Chronic mucocutaneous candidiasis Chronic granulomatous disease Sweet syndrome Monocytopenia with susceptibility to infections Dermatomyositis Scleroderma