SE-ATLAS

Primary ciliary dyskinesia Dermatomyositis, juvenile Interstitielle Lungenkrankheit, sekundäre, spezifische, der Kindheit , mit assoziierter systemischer Vaskulitis Immundefekt mit Störung des Komplement-Aktivierungsweg Immundefekt durch CD25-Mangel Autosomal-dominante Suszeptibilität für Mykobakteriosen durch partiellen Defekt LIG4-Syndrom Barth-Syndrom Primäre Ziliendyskinesie - Retinitis pigmentosa Cryopyrin-assoziiertes periodisches Syndrom JMP-Syndrom Interstitielle Lungenkrankheit, sekundäre, spezifische, der Kindheit , mit assoziierter Granulomatose Pneumonie, chronische, des Kindesalters Ataxia-Teleangiectasia-ähnliche Krankheit PAPA-Syndrom Immundefekt, primärer Interstitielle Lungenkrankheit, Strahleninduzierte Sarkoidose Autosomal-rezessive Suszeptibilität für Mykobakteriosen durch partiellen Defekt Tuberkulose Interstitielle Lungenkrankheit, sekundäre, spezifische, der Kindheit , mit assoziierter Stoffwechselkrankheit Immuno-neurologische Krankheit, X-chromosomale Gelbe-Nägel-Syndrom Skelettdysplasie mit verkürzten Extremitäten und schwerem kombinierten Immundefekt Kombinierter Immundefekt durch IL21R-Mangel Castleman-Krankheit des Kindesalters Panbronchiolitis, diffuse Komplement-Komponente 3-Mangel Immundefekt, kombinierter schwerer, durch DOCK8-Mangel Pneumonie, interstitielle, unspezifische Suszeptibilität für Mykobakteriosen durch kompletten IL12RB1-Defekt Asbestintoxifikation Suszeptibilität für Mykobakteriosen durch kompletten IFN-gamma-R2-Defekt Vaskulitis mit assoziierten antineutrophilen zytoplasmatischen Antikörpern Lungenfibrose, idiopathische Lupus erythematodes, systemischer, des Kindesalters Lymphoproliferative Krankheit, X-chromosomale Defekt der schweren Immunglobulinkette Autoimmun-lymphoproliferatives Syndrom CANDLE-Syndrom Riesenzell-Arteriitis Genetische Prädisposition für Infektionen durch spezifische Pathogene Bloom-Syndrom Kälte-Urtikaria, familiäre Suszeptibilität für Mykobakteriosen durch kompletten IL12B-Defekt Immundefekt, kombinierter schwerer, durch LCK-Mangel Mischkollagenose Neutrophiles Immundefekt-Syndrom Langerhans-Zell-Histiozytose der Kindheit Osteopetrose-Hypogammaglobulinämie-Syndrom Lymphangioleiomyomatose Vici-Syndrom Lymphohistiozytose, hämophagozytische, familiäre Form Say-Barber-Miller-Syndrom Hyper-IgE-Syndrom, autosomal-dominantes Suszeptibilität für Bakterieninfektion durch TLR Signalweg-Defizienz Myeloperoxidase-Mangel Vaskulitis, hypokomplementämische urtikarielle Papillon-Lefèvre-Syndrom Beryllium-Krankheit, chronische Interstitielle Lungenkrankheit des Erwachsenen Hirn-Lunge-Schilddrüsen-Syndrom Empfänglichkeit für virale und mykobakterielle Infektionen durch STAT1-Defizienz Gesichtsdysmorphie-Immundefekt-Livedo-Kleinwuchs-Syndrom CREST-Syndrom T-Zell-Immundefekt mit Thymusaplasie Autosomal-rezessive Suszeptibilität für Mykobakteriosen durch partiellen IFN-gamma-R1-Defekt Hajdu-Cheney-Syndrom Primäre interstitielle Lungenkrankheit des Erwachsenen Schweres akutes respiratorisches Syndrom Dyskeratosis congenita Suszeptibilität für Mykobakteriosen durch kompletten ISG15-Defekt Immundefekt, kombinierter schwerer, durch DCLRE1C-Mangel Immundefekt, kombinierter schwerer, durch Gamma-Ketten-Defekt, T- B+ Primäres Immundefekt-Syndrom durch LAMTOR2-Defizienz Immundefekt, kombinierter schwerer, durch Adenosin-Desaminase-Mangel Polymyositis, juvenile Autosomal-rezessive Suszeptibilität für Mykobakteriosen durch partiellen IFN-gamma-R2-Defekt Frühgeborenen-Apnoe Immundefekt, kombinierter, mit Granulomatose Autoimmun-lymphoproliferative Krankheit vom Typ Dianzani Agammaglobulinämie-Mikrozephalie-Kraniosynostose-schwere Dermatitis-Syndrom Glykogenose, interstitielle pulmonale Lungenfibrose - Immundefekt - Gonadendysgenesie Autoimmun-lymphoproliferatives Syndrom mit rezidivierenden Infekten Interstitielle Lungenkrankheit Kawasaki-Krankheit Interstitielle Lungenkrankheit, sekundäre, spezifische, des Erwachsenen , mit assoziierter systemischer Krankheit Mikrolithiasis, alveoläre pulmonale Asplenie, familiäre isolierte, kongenitale Takayasu-Arteriitis Hyperzinkämie und Hypercalprotectinämie Hyperplasie, lymphoide pulmonale noduläre Pneumokoniose Neutropenie, kongenitale schwere, autosomal-rezessive, durch G6PC3-Mangel Rekurrente Infektionen durch spezifischen Granulamangel Neuroendokrine Zellhyperplasie der Kindheit Arthritis, idiopathische juvenile, oligoartikuläre, mit anti-nukleären Antikörpern Transiente Hypogammaglobulinämie der Kindheit Lebervenen-Verschlusskrankheit - Immunschwäche Vaskulitis, postinfektiöse Langerhans-Zell-Histiozytose des Erwachsenen Pearson-Syndrom Pneumonie, interstitielle, akute Interstitielle Lungenkrankheit des Kindes/Erwachsenen Aktivierendes PIK3-delta-Syndrom Sekundäre interstitielle Lungenkrankheit im Kindes- und Erwachsenenalter mit assoziierter Bindegewebsstörung Chronische Atemnot mit Stoffwechseldefekt des Surfactant-Systems Arthritis, reaktive Papillomatose, rekurrente respiratorische Immundefekt durch klassischen Komponentenmangel des Komplementsystems Bronchiektasie, idiopathische Autosomal-dominante Suszeptibilität für Mykobakteriosen durch partiellen IFN-gamma-R1-Defekt Pneumonie, interstitielle, lymphoide Akute neonatale Atemnot durch SP-B-Mangel Pneumonie, eosinophile idiopathische Herpes-simplex-Enzephalitis Autoinflammatorisches Syndrom der Kindheit Respiratorische Bronchiolitis mit interstitieller Lungenerkrankung Deletion 22q11 Immundefekt durch Komplementdefekt bei Störung einer späten Komponente Immundefekt, kombinierter schwerer, durch CARD11-Mangel Arthritis, idiopathische juvenile, oligoartikuläre, ohne anti-nukleäre Antikörper Suszeptibilität für Mykobakteriosen durch partielle STAT1-Defizienz Immundefekt durch MHC Klasse II-Expressionsdefekt Immundefekt, kombinierter schwerer, T- B+, durch IL-7Ralpha-Mangel Immundefekt, kombinierter schwerer, T- B+ infolge JAK3-Mangel Fasziitis, eosinophile Nijmegen-Breakage-Syndrom-ähnliche Krankheit Arthritis, idiopathische juvenile polyartikuläre, Rheumafaktor-negative Muckle-Wells-Syndrom Autosomal-dominante Suszeptibilität für Mykobakteriosen durch partiellen IFN-gamma-R2-Defekt Epidermodysplasia verruciformis Kryoglobulinämische Vaskulitis Siegler-Brewer-Carey-Syndrom PLCG2-associated antibody deficiency and immune dysregulation Konstitutionelle Neutropenie mit extrahämatopoetischen Manifestationen Arthritis, idiopathische juvenile, oligoartikuläre Interstitielle Lungenkrankheit, primäre, des Kindes/Erwachsenen Chédiak-Higashi-Syndrom Agammaglobulinämie, isolierte Suszeptibilität für Mykobakteriosen durch partiellen IRF8-Defekt Arthritis, idiopathische juvenile, unklassifizierte Sonstiges Immundefekt-Syndrom durch Störung der adaptiven Immunität Immundefekt, kombinierter schwerer, T-B- Omenn-Syndrom Arthritis, idiopathische juvenile, systemische Immundefekt, kombinierter schwerer, T- B+, durch CD45-Mangel Arthritis, idiopathische juvenile, Rheumafaktor-negative, mit anti-nukleären Antikörpern Arthritis, idiopathische juvenile, Rheumafaktor-negative, ohne anti-nukleäre Antikörper Agammaglobulinämie, syndromale Immundefekt durch Ficolin-3-Mangel Interstitielle Lungenkrankheit-Nephrotisches Syndrom-Epidermolysis bullosa-Syndrom Immundefekt, kombinierter schwerer, T-B+ Immundefekt, kombinierter schwerer, T- B+, durch CD3delta/CD3epsilon/CD3zeta-Defekt Immundefekt, kombinierter, durch STK4-Mangel Cartilage-hair hypoplasia Familial spontaneous pneumothorax Roifman syndrome Cystic fibrosis Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome Polyarticular juvenile idiopathic arthritis X-linked severe congenital neutropenia Combined immunodeficiency due to ORAI1 deficiency Combined immunodeficiency due to STIM1 deficiency Autoimmune polyendocrinopathy type 1 Diffuse alveolar hemorrhage Hereditary periodic fever syndrome Microscopic polyangiitis NLRP12-associated hereditary periodic fever syndrome X-linked mendelian susceptibility to mycobacterial diseases Kostmann syndrome Relapsing polychondritis Eosinophilic granulomatosis with polyangiitis Severe congenital neutropenia X-linked agammaglobulinemia Severe combined immunodeficiency due to DNA-PKcs deficiency Blau syndrome Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells Autoinflammatory syndrome with immune deficiency Hoyeraal-Hreidarsson syndrome Periodic fever syndrome of childhood Combined immunodeficiency with facio-oculo-skeletal anomalies 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 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 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 Sterile multifocal osteomyelitis with periostitis and pustulosis Familial Mediterranean fever 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 Common variable immunodeficiency Lichtenstein syndrome Infant acute respiratory distress syndrome Gorham-Stout disease Allergic bronchopulmonary aspergillosis Susceptibility to infection due to TYK2 deficiency Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease Tracheobronchopathia osteochondroplastica Cryptogenic organizing pneumonia Severe combined immunodeficiency FADD-related immunodeficiency Hereditary pulmonary alveolar proteinosis Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Meconium aspiration syndrome Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Bronchiolitis obliterans Idiopathic recurrent pericarditis Reticular dysgenesis Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis Infantile apnea Autosomal dominant severe congenital neutropenia Hyper-IgM syndrome with susceptibility to opportunistic infections Immunodeficiency due to selective anti-polysaccharide antibody deficiency Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells Purine nucleoside phosphorylase deficiency Immunoglobulin A vasculitis Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency Unexplained periodic fever syndrome of childhood Overlapping connective tissue disease Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome WHIM syndrome Congenital alveolar capillary dysplasia Selective IgM deficiency Spondyloenchondrodysplasia Granulomatosis with polyangiitis DNA repair defect other than combined T-cell and B-cell immunodeficiencies Other immunodeficiency syndrome with predominantly antibody defects Primary interstitial lung disease specific to childhood due to alveolar vascular disorder Langerhans cell histiocytosis in childhood and adulthood Rare pediatric systemic disease Immunodeficiency by defective expression of MHC class I Hyper-IgM syndrome without susceptibility to opportunistic infections Idiopathic juvenile osteoporosis ICF syndrome Combined T and B cell immunodeficiency Idiopathic CD4 lymphocytopenia Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells Cernunnos-XLF deficiency PFAPA syndrome Absent thumb-short stature-immunodeficiency syndrome Wiskott-Aldrich syndrome CINCA syndrome Congenital chylothorax Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome Rare pediatric vasculitis Tumor necrosis factor receptor 1 associated periodic syndrome Agammaglobulinemia Immuno-osseous dysplasia Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome Secondary pulmonary hemosiderosis Combined immunodeficiency due to CD3gamma deficiency Juvenile idiopathic arthritis Severe combined immunodeficiency due to CORO1A deficiency Immunodeficiency syndrome with autoimmunity Combined immunodeficiency due to CD27 deficiency Congenital neutropenia-myelofibrosis-nephromegaly syndrome Combined immunodeficiency due to ZAP70 deficiency Drug-induced vasculitis Isolated pulmonary capillaritis Poikiloderma with neutropenia Recurrent infections associated with rare immunoglobulin isotypes deficiency Staphylococcal necrotizing pneumonia Immunodeficiency predominantly affecting antibody production Idiopathic pulmonary hemosiderosis Congenital diaphragmatic hernia Cyclic neutropenia Primary hemophagocytic lymphohistiocytosis Lymphoproliferative syndrome Immunodeficiency syndrome with hypopigmentation Pancytopenia due to IKZF1 mutations T-cell immunodeficiency with epidermodysplasia verruciformis Congenital pulmonary lymphangiectasia Functional neutrophil defect Proteasome-associated autoinflammatory syndrome Hypersensitivity pneumonitis Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease Idiopathic interstitial pneumonia X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia Unclassified vasculitis Combined pulmonary fibrosis-emphysema syndrome Neutropenia-monocytopenia-deafness syndrome Interstitial lung disease specific to infancy Susceptibility to respiratory infections associated with CD8alpha chain mutation Combined immunodeficiency due to CRAC channel dysfunction Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome Ataxia-telangiectasia Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis Majeed syndrome Constitutional neutropenia Nijmegen breakage syndrome Secondary interstitial lung disease specific to childhood associated with a systemic disease Anti-glomerular basement membrane disease Properdin deficiency Unexplained long-lasting fever/inflammatory syndrome Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency Cogan syndrome Syndromic multisystem autoimmune disease due to Itch deficiency Combined immunodeficiency due to partial RAG1 deficiency Leukocyte adhesion deficiency Desquamative interstitial pneumonia Primary immunodeficiency due to a defect in innate immunity Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency Drug or radiation exposure-related interstitial lung disease Autosomal agammaglobulinemia Severe dermatitis-multiple allergies-metabolic wasting syndrome Secondary interstitial lung disease specific to childhood associated with a connective tissue disease RAS-associated autoimmune leukoproliferative disease Sweet syndrome Chronic mucocutaneous candidiasis Chronic granulomatous disease Monocytopenia with susceptibility to infections Scleroderma Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency Behçet disease Severe combined immunodeficiency due to FOXN1 deficiency Acute lung injury Sudden infant death-dysgenesis of the testes syndrome Dermatomyositis Proximal Xq28 duplication syndrome Shwachman-Diamond syndrome Immunodeficiency due to MASP-2 deficiency Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis Interstitial lung disease specific to childhood