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 Autoimmune lymphoproliferative syndrome with recurrent viral infections Kawasaki disease Familial isolated congenital asplenia Pulmonary alveolar microlithiasis Secondary interstitial lung disease specific to adulthood associated with a systemic disease Takayasu arteritis Hyperzincemia and hypercalprotectinemia Pneumoconiosis Pulmonary nodular lymphoid hyperplasia Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency Neuroendocrine cell hyperplasia of infancy Recurrent infection due to specific granule deficiency Transient hypogammaglobulinemia of infancy Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies Hepatic veno-occlusive disease-immunodeficiency syndrome Postinfectious vasculitis Pearson syndrome Langerhans cell histiocytosis specific to adulthood Acute interstitial pneumonia Activated PI3K-delta syndrome Interstitial lung disease in childhood and adulthood Chronic respiratory distress with surfactant metabolism deficiency Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease Recurrent respiratory papillomatosis Reactive arthritis Immunodeficiency due to a classical component pathway complement deficiency Idiopathic bronchiectasis Lymphoid interstitial pneumonia Neonatal acute respiratory distress due to SP-B deficiency Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency Herpes simplex virus encephalitis Idiopathic eosinophilic pneumonia Respiratory bronchiolitis-interstitial lung disease syndrome Autoinflammatory syndrome of childhood 22q11.2 deletion syndrome Combined immunodeficiency due to CARD11 deficiency Immunodeficiency due to a late component of complement deficiency Immunodeficiency due to MASP-2 deficiency Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies T-B+ severe combined immunodeficiency due to JAK3 deficiency T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency Immunodeficiency by defective expression of MHC class II Nijmegen breakage syndrome-like disorder Eosinophilic fasciitis Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency Epidermodysplasia verruciformis Muckle-Wells syndrome Siegler-Brewer-Carey syndrome PLCG2-associated antibody deficiency and immune dysregulation Constitutional neutropenia with extra-hematopoietic manifestations Cryoglobulinemic vasculitis Oligoarticular juvenile idiopathic arthritis Chédiak-Higashi syndrome Isolated agammaglobulinemia Primary interstitial lung disease in childhood and adulthood Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency T-B- severe combined immunodeficiency Other immunodeficiency syndromes due to defects in innate immunity Unspecified juvenile idiopathic arthritis Omenn syndrome Systemic-onset juvenile idiopathic arthritis T-B+ severe combined immunodeficiency due to CD45 deficiency Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies Immunodeficiency due to ficolin3 deficiency Syndromic agammaglobulinemia T-B+ severe combined immunodeficiency Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta Combined immunodeficiency due to STK4 deficiency Familial spontaneous pneumothorax Cartilage-hair hypoplasia Roifman syndrome Cystic fibrosis Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome Polyarticular juvenile idiopathic arthritis Combined immunodeficiency due to ORAI1 deficiency X-linked severe congenital neutropenia Combined immunodeficiency due to STIM1 deficiency Diffuse alveolar hemorrhage Autoimmune polyendocrinopathy type 1 Hereditary periodic fever syndrome Microscopic polyangiitis X-linked mendelian susceptibility to mycobacterial diseases Kostmann syndrome NLRP12-associated hereditary periodic fever syndrome Relapsing polychondritis Eosinophilic granulomatosis with polyangiitis Severe congenital neutropenia Severe combined immunodeficiency due to DNA-PKcs deficiency X-linked agammaglobulinemia Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells Blau syndrome Autoinflammatory syndrome with immune deficiency Hoyeraal-Hreidarsson syndrome Combined immunodeficiency with facio-oculo-skeletal anomalies Periodic fever syndrome of childhood Deficiency in anterior pituitary function-variable immunodeficiency syndrome Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation Severe combined immunodeficiency due to complete RAG1/2 deficiency Mixed autoinflammatory and autoimmune syndrome Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Psoriasis-related juvenile idiopathic arthritis Immunodeficiency with factor I anomaly Cohen syndrome Schimke immuno-osseous dysplasia Immunodeficiency due to absence of thymus Enthesitis-related juvenile idiopathic arthritis Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency Acute lung injury Interstitial lung disease specific to childhood 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 Apnée infantile Déficit immunitaire par déficit sélectif en anticorps anti-polysaccharide Déficit immunitaire avec déficit d'isotype ou de chaînes légères et nombre normal de cellules B Syndrome hyper-IgM avec susceptibilité aux infections opportunistes Déficit en purine nucléoside phosphorylase Déficit immunitaire par déficit en IRAK4 Vascularite à immunoglobulines A Maladie de chevauchement du tissu conjonctif Fièvre récurrente inexpliquée de l'enfant Syndrome WHIM Syndrome de dérèglement immunitaire-polyendocrinopathie-entéropathie lié à l'X Dysplasie alvéolo-capillaire congénitale Déficit sélectif en IgM Granulomatose avec polyangéite Dysplasie spondylo-enchondrale Autre syndrome de déficit immunitaire par déficit de production d'anticorps Anomalie de réparation de l'ADN autre qu'un déficit immunitaire combiné à cellules B et T Pneumopathie interstitielle primaire spécifique de l'enfance due à une anomalie vasculaire des alvéoles Histiocytose langerhansienne de l'enfant et de l'adulte Maladie systémique rare de l'enfant Syndrome hyper-IgM sans susceptibilité aux infections opportunistes Déficit immunitaire par déficit d'expression des molécules CMH de classe I Syndrome ICF Ostéoporose idiopathique juvénile Déficit immunitaire combiné T et B Déficit immunitaire avec diminution sévère des IgG et IgA et taux normal ou élevé d'IgM avec nombre normal de cellules B Lymphocytopénie CD4 idiopathique Syndrome CINCA Chylothorax congénital Syndrome des pouces absents-petite taille-déficit immunitaire Syndrome PFAPA Syndrome de Wiskott-Aldrich Déficit en cernunnos-XLF Syndrome de poïkilodermie héréditaire fibrosante-myopathie rétractile-fibrose pulmonaire Vascularite rare de l'enfant Agammaglobulinémie Syndrome périodique associé au récepteur 1 du facteur de nécrose tumorale Dysplasie immuno-osseuse Syndrome de fibrose pulmonaire-hyperplasie hépatique-hypoplasie de la moelle osseuse Déficit immunitaire combiné par déficit en CD3gamma Hémosidérose pulmonaire secondaire Arthrite juvénile idiopathique Syndrome de déficit immunitaire avec auto-immunité Déficit immunitaire combiné par déficit en CD27 Déficit immunitaire combiné sévère par déficit en CORO1A Syndrome de neutropenie congénitale-myélofibrose-néphromégalie Vascularite induite par les médicaments Capillarite pulmonaire isolée Déficit immunitaire combiné par déficit en ZAP70 Poïkilodermie avec neutropénie Pneumonie nécrosante staphylococcique Infection récurrente associée à un déficit rare en isotype d'immunoglobuline Hémosidérose pulmonaire idiopathique Hernie de coupole diaphragmatique Neutropénie cyclique Lymphohistiocytose hémophagocytaire primaire Déficit immunitaire par déficit de production d'anticorps Syndrome lymphoprolifératif Syndrome de déficit immunitaire et hypopigmentation Déficit immunitaire à cellules T avec épidermodysplasie verruciforme Lymphangiectasie pulmonaire congénitale Déficit fonctionnel des neutrophiles Pancytopénie par mutations de IKZF1 Alvéolite allergique extrinsèque Syndrome auto-inflammatoire lié au protéasome Pneumopathie interstitielle secondaire de l'enfant et de l'adulte associée à une maladie métabolique Pneumonie interstitielle idiopathique Vascularite non classifiée Déficit immunitaire lié à l'X avec déficit en magnésium, infection et néoplasie liées au virus Epstein-Barr Syndrome de neutropénie-monocytopénie-surdité Pneumopathie interstitielle spécifique de la petite enfance Syndrome d'emphysème-fibrose pulmonaire combinés Déficit immunitaire combiné par dysfonctionnement du canal CRAC Susceptibilité aux infections respiratoires associée à une mutation de la chaîne alpha de CD8 Syndrome d'anémie sidéroblastique congénitale-déficit immunitaire en cellules B-fièvre périodique-retard de développement Ataxie-télangiectasie Syndrome de Majeed Pneumopathie interstitielle secondaire de l'enfant et de l'adulte associée à une vascularite systémique Neutropénie constitutionnelle Syndrome de Nijmegen Pneumopathie interstitielle secondaire spécifique de l'enfance associée à une maladie systémique Déficit en properdine Syndrome inflammatoire/fièvre de longue durée inexpliquée Maladie des anticorps anti-membrane basale glomérulaire Prédisposition mendélienne autosomique récessive aux infections mycobactériennes par déficit complet Syndrome de Cogan Déficit immunitaire combiné par déficit partiel en RAG1 Déficit d'adhésion leucocytaire Maladie auto-immune multisystémique syndromique par déficit en Itch Agammaglobulinémie autosomique Pneumonie interstitielle desquamative Déficit immunitaire primaire avec déficit en cellules NK et insuffisance surrénale Pneumopathie interstitielle médicamenteuse ou secondaire à une exposition aux radiations Déficit immunitaire primaire par défaut de l'immunité innée Syndrome de dermatite sévère-allergies multiples-cachexie métabolique Déficit immunitaire combiné sévère par déficit en FOXN1 Maladie leucoproliférative auto-immune associée à RAS Pneumopathie interstitielle secondaire spécifique de l'enfance associée à une maladie du tissu conjonctif Candidose cutanéo-muqueuse chronique Granulomatose chronique Syndrome de Sweet Monocytopénie avec susceptibilité aux infections Dermatomyosite Sclérodermie