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 Autoinflammatorisches Syndrom, unklassifiziertes, der Kindheit Suszeptibilität für Mykobakteriosen, familiäre Form Hypohidrotische ektodermale Dysplasie mit Immundefekt Allergische Wohnungs-Alveolitis Interstitielle Lungenkrankheit, primäre spezifische, der Kindheit Farmerlungen-Krankheit Alveolitis, allergische berufsbedingte Mittelmeerfieber, familiäres Sterile multifokale Osteomyelitis mit Periostitis und Pustulose Hyper IgE-Syndrom Interstitielle Lungenkrankheit, sekundäre, des Kindes/Erwachsenen Taubenzüchter-Lungenkrankheit Pannikulitis mit Uveitis und systemischer Granulomatose, infantile Form Autoinflammatorisches Syndrom, granulomatöses, der Kindheit Interstitielle Lungenkrankheit durch alveoläre Strukturanomalien, primäre spezifische, der Kindheit Neisseria-Infektionen, rekurrente, durch Faktor D-Mangel Lichtenstein-Syndrom Akutes Atemnotsyndrom des Kindes Immundefektsyndrom, variables Aspergillose, allergische bronchopulmonale Gorham-Stout-Krankheit Suszeptibilität für Infektionen durch TYK2-Mangel Interstitielle Lungenkrankheit, sekundäre, des Kindes/Erwachsenen, mit assoziierter systemischer Krankheit Pneumonie, kryptogene organisierende Immundefekt, kombinierter schwerer FADD-abhängiger Immundefekt Pulmonale Alveolarproteinose, hereditäre Form Tracheobronchopathia osteochondroplastica Mekonium-Aspirationssyndrom Primäre interstitielle Lungenerkrankung des Kindesalters durch pulmonale Surfactant-Protein-Anomalie Anhidrotische ektodermale Dysplasie-Immundefekt-Osteopetrose-Lymphödem-Syndrom Bronchiolitis obliterans mit obstruktiver Lungenerkrankung Perikarditis, idiopathische rekurrente Chronische nicht-bakterielle Osteomyelitis/rezidivierende multifokale Osteomyelitis Retikuläre Dysgenesie Neutropenie, kongenitale schwere, autosomal-dominante Apnoe, infantile Immundefekt durch selektiven Antipolysaccharid-Antikörper-Mangel Immundefekt mit Isotypen- oder Leichtketten-Mangel und normaler Anzahl B-Zellen Hyper-IgM-Syndrom mit opportunistischen Infektionen Purin-Nukleosid-Phosphorylase-Mangel Immundefekt durch Interleukin-1-Rezeptor-assoziierten Kinase-4-Mangel Immunoglobulin A-Vaskulitis Mischkollagenose, überlappende Unerklärliches periodisches Fierbersyndrom der Kindheit WHIM-Syndrom Immundysregulation-Polyendokrinopathie-Enteropathie-Syndrom, X-chromosomales Dysplasie, alveolar-kapilläre, kongenitale IgM-Mangel, selektiver Granulomatose mit Polyangiitis Spondyloenchondrodysplasie Sonstige Immundefekt-Syndrome mit vorwiegendem Antikörper-Defekt DNA-Reparaturdefekt, ungleich kombinierter B- und T-Zell-Immundefekt Interstitielle Lungenkrankheit durch alveoläre Vaskulationsstörungen, primäre spezifische, der Kindheit Langerhans-Zell-Histiozytose des Kindes/Erwachsenen Seltene systemische Krankheit des Kindes Hyper-IgM-Syndrom ohne opportunistische Infektionen Immundefekt durch MHC Klasse I-Expressionsdefekt ICF-Syndrom Osteoporose, idiopathische juvenile T- und B-Zell-Immundefekt, kombinierter Immundefekt mit starker Reduktion von Serum-IgG und Serum-IgA bei normalem/erhöhtem IgM-Level und normaler Anzahl B-Zellen CD4-Lymphozytopenie, idiopathische CINCA-Syndrom Chylothorax, kongenitale Fehlende Daumen-Kleinwuchs-Immundefekt-Syndrom PFAPA-Syndrom Wiskott-Aldrich-Syndrom Cernunnos/XLF-Mangel Hereditäre fibröse Poikilodermie-Sehnenkontraktur-Myopathie-Lungenfibrose-Syndrom Seltene Vaskulitis des Kindes Agammaglobulinämie Tumornekrosefaktor-Rezeptor 1-assoziiertes periodisches Fieber-Syndrom Dysplasie, immuno-ossäre Lungenfibrose - Leberhyperplasie - Knochenmarkhypoplasie Immundefekt, kombinierter, durch CD3-gamma-Mangel Lungen-Hämosiderose, sekundäre Arthritis, idiopathische juvenile Immundefekt-Syndrom mit Autoimmunität Lymphoproliferative Krankheit, autosomal-rezessive Immundefekt, kombinierter schwerer, durch CORO1A-Mangel Rezidivierende Infekte-Myelofibrose-Nephromegalie-Syndrom Vaskulitis, Medikamenten-induzierte Lungen-Kapillaritis, isolierte Immundefekt, kombinierter, durch ZAP70-Mangel Poikilodermie mit Neutropenie Pneumonie, nekrotisierende, Staphylokokken-induzierte Rezidivierende Infekte mit assoziierten Immunoglobulin-Isotypen Lungen-Hämosiderose, idiopathische Zwerchfellhernie, kongenitale Neutropenie, zyklische Lymphohistiozytose, hämophagozytische, primäre Immundefekt mit vorwiegender Beeinträchtigung der Antikörper-Produktion Lymphoproliferatives Syndrom Immundefekt-Syndrom mit Hypopigmentierung T-Zell-Immundefekt mit Epidermodysplasia verruciformis Lymphangiektasie, pulmonale, kongenitale Schwere rekurrente Infektionen mit neutrophiler Dysfunktion Panzytopenie durch IKZF1-Genmutationen Hypersensitivitätspneumonie Proteasom-assoziiertes autoinflammatorisches Syndrom Sekundäre interstitielle Lungenkrankheit des Kindes/Erwachsenen mit assoziierter Stoffwechselkrankheit Pneumonie, interstitielle, idiopathische Vaskulitis, unklassifizierte Immundefekt, X-chromosomaler, mit Magnesium-Defekt, Epstein-Barr-Virus-Infektion und Neoplasie Neutropenie - Monozytopenie - Schwerhörigkeit Interstitielle Lungenkrankheit, spezifische, des Kleinkindes Kombiniertes pulmonales fibrosierendes Emphysem-Syndrom Immundefekt, kombinierter, durch Defekt des CRAC-Kanals Erhöhte Anfälligkeit für Atemwegsinfektionen durch CD8alpha-Defizienz Kongenitale sideroblastische Anämie-B-Zell-Immundefekt-periodisches Fieber-Entwicklungsverzögerung-Syndrom Ataxia-Teleangiectasia Majeed-Syndrom Sekundäre interstitielle Lungenkrankheit des Kindes/Erwachsenen mit assoziierter systemischer Vaskultits Neutropenie, konstitutionelle Nijmegen-Chromosomenbruch-Syndrom Interstitielle Lungenkrankheit, sekundäre, spezifische, der Kindheit , mit assoziierter systemischer Krankheit Properdin-Mangel Fieber-Syndrom, langanhaltendes unerklärbares Antikörper vermittelte Krankheit der glomerulären Basalmembran Autosomal-rezessive Suszeptibilität für Mykobakteriosen durch kompletten Defekt Cogan-Syndrom Immundefekt, kombinierter, durch partiellen RAG1-Mangel Leukozytenadhäsionsdefekt Autoimmunkrankheit, multisystemische syndromale, durch Itch-Mangel Agammaglobulinämie, autosomal-rezessive Desquamative interstitielle Pneumonie Primärer Immundefekt mit Mangel der natürlichen Killerzellen und Nebenniereninsuffizienz Interstitielle Lungenkrankheit, Substanz- oder Strahleninduzierte Primärer Immundefekt durch Anomalie des angeborenen Immunsystems Schwere Dermatitis-multiple Allergien-metabolischer Verlust-Syndrom Immundefekt, kombinierter schwerer, durch FOXN1-Defizienz RAS-assoziierte autoimmun-lymphoproliferative Krankheit Interstitielle Lungenkrankheit, sekundäre, spezifische, der Kindheit , mit assoziierter Bindegewebskrankheit Candidose, chronische mukokutane Granulomatose, chronische Sweet-Syndrom Monozytopenie mit erhöhter Infektionsanfälligkeit Dermatomyositis Sklerodermie