Klinik für Pädiatrie mit Schwerpunkt Pneumologie, Immunologie und Intensivmedizin an der Charité Berlin Assigned diseases:
In the following you will find the diseases that are treated in this facility:
16q24.1 microdeletion syndrome
22q11.2 deletion syndrome
Absent thumb-short stature-immunodeficiency syndrome
Activated PI3K-delta syndrome
Acute interstitial pneumonia
Acute lung injury
Adult acute respiratory distress syndrome
Adult pulmonary Langerhans cell histiocytosis
Agammaglobulinemia
Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
Allergic bronchopulmonary aspergillosis
Alpha-1-antitrypsin deficiency
Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
Anti-glomerular basement membrane disease
Anti-neutrophil cytoplasmic antibody-associated vasculitis
Apnea of prematurity
Asbestos intoxication
Ataxia-telangiectasia
Ataxia-telangiectasia-like disorder
Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome
Autoimmune lymphoproliferative syndrome
Autoimmune lymphoproliferative syndrome with recurrent viral infections
Autoimmune polyendocrinopathy type 1
Autoimmune pulmonary alveolar proteinosis
Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation
Autoinflammatory syndrome of childhood
Autoinflammatory syndrome with immune deficiency
Autosomal agammaglobulinemia
Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
Autosomal dominant severe congenital neutropenia
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
Bacterial susceptibility due to TLR signaling pathway deficiency
Barth syndrome
Behçet disease
Blau syndrome
Bloom syndrome
Brain-lung-thyroid syndrome
Bronchiolitis obliterans
CANDLE syndrome
CINCA syndrome
CREST syndrome
Cartilage-hair hypoplasia
Cernunnos-XLF deficiency
Chronic beryllium disease
Chronic granulomatous disease
Chronic mucocutaneous candidiasis
Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis
Chronic pneumonitis of infancy
Chronic respiratory distress with surfactant metabolism deficiency
Chédiak-Higashi syndrome
Cogan syndrome
Cohen syndrome
Combined T and B cell immunodeficiency
Combined immunodeficiency due to CARD11 deficiency
Combined immunodeficiency due to CD27 deficiency
Combined immunodeficiency due to CD3gamma deficiency
Combined immunodeficiency due to CRAC channel dysfunction
Combined immunodeficiency due to DOCK8 deficiency
Combined immunodeficiency due to IL21R deficiency
Combined immunodeficiency due to ORAI1 deficiency
Combined immunodeficiency due to STIM1 deficiency
Combined immunodeficiency due to STK4 deficiency
Combined immunodeficiency due to ZAP70 deficiency
Combined immunodeficiency due to partial RAG1 deficiency
Combined immunodeficiency with facio-oculo-skeletal anomalies
Combined immunodeficiency with granulomatosis
Combined pulmonary fibrosis-emphysema syndrome
Common variable immunodeficiency
Complement component 3 deficiency
Congenital alveolar capillary dysplasia
Congenital chylothorax
Congenital diaphragmatic hernia
Congenital neutropenia-myelofibrosis-nephromegaly syndrome
Congenital pulmonary lymphangiectasia
Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
Constitutional neutropenia
Constitutional neutropenia with extra-hematopoietic manifestations
Cryoglobulinemic vasculitis
Cryptogenic organizing pneumonia
Cyclic neutropenia
Cystic fibrosis
DNA repair defect other than combined T-cell and B-cell immunodeficiencies
Deficiency in anterior pituitary function-variable immunodeficiency syndrome
Desquamative interstitial pneumonia
Dianzani autoimmune lymphoproliferative disease
Diffuse alveolar hemorrhage
Diffuse panbronchiolitis
Drug or radiation exposure-related interstitial lung disease
Drug-induced vasculitis
Dyskeratosis congenita
Enthesitis-related juvenile idiopathic arthritis
Eosinophilic fasciitis
Eosinophilic granulomatosis with polyangiitis
Epidermodysplasia verruciformis
Exposure-related interstitial lung disease
FADD-related immunodeficiency
Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
Familial Mediterranean fever
Familial cold urticaria
Familial hemophagocytic lymphohistiocytosis
Familial isolated congenital asplenia
Familial spontaneous pneumothorax
Farmer's lung disease
Functional neutrophil defect
Genetic susceptibility to infections due to particular pathogens
Giant cell arteritis
Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib
Gorham-Stout disease
Granulomatosis with polyangiitis
Granulomatous autoinflammatory syndrome of childhood
Griscelli syndrome type 2
Hajdu-Cheney syndrome
Hashimoto-Pritzker syndrome
Heiner syndrome
Hepatic veno-occlusive disease-immunodeficiency syndrome
Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome
Hereditary periodic fever syndrome
Hereditary pulmonary alveolar proteinosis
Hermansky-Pudlak syndrome due to AP-3 deficiency
Herpes simplex virus encephalitis
House allergic alveolitis
Hoyeraal-Hreidarsson syndrome
Hyper-IgE syndrome
Hyper-IgM syndrome type 2
Hyper-IgM syndrome type 3
Hyper-IgM syndrome type 4
Hyper-IgM syndrome type 5
Hyper-IgM syndrome with susceptibility to opportunistic infections
Hyper-IgM syndrome without susceptibility to opportunistic infections
Hyperimmunoglobulinemia D with periodic fever
Hypersensitivity pneumonitis
Hyperzincemia and hypercalprotectinemia
Hypocomplementemic urticarial vasculitis
Hypohidrotic ectodermal dysplasia with immunodeficiency
ICF syndrome
Idiopathic CD4 lymphocytopenia
Idiopathic bronchiectasis
Idiopathic eosinophilic pneumonia
Idiopathic interstitial pneumonia
Idiopathic juvenile osteoporosis
Idiopathic pulmonary fibrosis
Idiopathic pulmonary hemosiderosis
Idiopathic recurrent pericarditis
Immune dysregulation disease with immunodeficiency
Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
Immuno-osseous dysplasia
Immunodeficiency by defective expression of MHC class I
Immunodeficiency by defective expression of MHC class II
Immunodeficiency due to CD25 deficiency
Immunodeficiency due to MASP-2 deficiency
Immunodeficiency due to a classical component pathway complement deficiency
Immunodeficiency due to a complement cascade protein anomaly
Immunodeficiency due to a late component of complement deficiency
Immunodeficiency due to absence of thymus
Immunodeficiency due to ficolin3 deficiency
Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency
Immunodeficiency due to selective anti-polysaccharide antibody deficiency
Immunodeficiency predominantly affecting antibody production
Immunodeficiency syndrome with autoimmunity
Immunodeficiency syndrome with hypopigmentation
Immunodeficiency with factor H anomaly
Immunodeficiency with factor I anomaly
Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells
Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells
Immunoglobulin A vasculitis
Immunoglobulin heavy chain deficiency
Infant acute respiratory distress syndrome
Infantile apnea
Infantile onset panniculitis with uveitis and systemic granulomatosis
Interstitial lung disease
Interstitial lung disease in childhood and adulthood
Interstitial lung disease specific to adulthood
Interstitial lung disease specific to childhood
Interstitial lung disease specific to infancy
Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome
Isolated agammaglobulinemia
Isolated pulmonary capillaritis
JMP syndrome
Juvenile dermatomyositis
Juvenile idiopathic arthritis
Juvenile polymyositis
Kawasaki disease
Kostmann syndrome
LIG4 syndrome
Langerhans cell histiocytosis in childhood and adulthood
Langerhans cell histiocytosis specific to adulthood
Langerhans cell histiocytosis specific to childhood
Laron syndrome with immunodeficiency
Letterer-Siwe disease
Leukocyte adhesion deficiency
Leukocyte adhesion deficiency type I
Leukocyte adhesion deficiency type II
Leukocyte adhesion deficiency type III
Lichtenstein syndrome
Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome
Lymphangioleiomyomatosis
Lymphoid interstitial pneumonia
Lymphoproliferative syndrome
Majeed syndrome
Meconium aspiration syndrome
Mendelian susceptibility to mycobacterial diseases
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Microscopic polyangiitis
Mixed autoinflammatory and autoimmune syndrome
Mixed connective tissue disease
Mixed cryoglobulinemia type II
Mixed cryoglobulinemia type III
Monocytopenia with susceptibility to infections
Muckle-Wells syndrome
Myeloperoxidase deficiency
NLRP12-associated hereditary periodic fever syndrome
NLRP3-associated autoinflammatory disease
Nakajo-Nishimura syndrome
Neonatal acute respiratory distress due to SP-B deficiency
Neuroendocrine cell hyperplasia of infancy
Neutropenia-monocytopenia-deafness syndrome
Neutrophil immunodeficiency syndrome
Nijmegen breakage syndrome
Nijmegen breakage syndrome-like disorder
Non-specific interstitial pneumonia
Occupational allergic alveolitis
Oligoarticular juvenile idiopathic arthritis
Oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies
Oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies
Omenn syndrome
Osteopetrosis-hypogammaglobulinemia syndrome
Other immunodeficiency syndrome with predominantly antibody defects
Other immunodeficiency syndromes due to defects in innate immunity
Overlapping connective tissue disease
PAPA syndrome
PFAPA syndrome
PLCG2-associated antibody deficiency and immune dysregulation
Pancytopenia due to IKZF1 mutations
Papillon-Lefèvre syndrome
Pearson syndrome
Pediatric Castleman disease
Pediatric systemic lupus erythematosus
Periodic fever syndrome of childhood
Pigeon-breeder lung disease
Pneumoconiosis
Poikiloderma with neutropenia
Polyarticular juvenile idiopathic arthritis
Postinfectious vasculitis
Primary ciliary dyskinesia
Primary ciliary dyskinesia-retinitis pigmentosa syndrome
Primary hemophagocytic lymphohistiocytosis
Primary immunodeficiency
Primary immunodeficiency due to a defect in adaptive immunity
Primary immunodeficiency due to a defect in innate immunity
Primary immunodeficiency syndrome due to LAMTOR2 deficiency
Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
Primary interstitial lung disease in childhood and adulthood
Primary interstitial lung disease in childhood and adulthood due to alveolar structure disorder
Primary interstitial lung disease in childhood and adulthood due to alveolar vascular disorder
Primary interstitial lung disease specific to adulthood
Primary interstitial lung disease specific to childhood
Primary interstitial lung disease specific to childhood due to alveolar structure disorder
Primary interstitial lung disease specific to childhood due to alveolar vascular disorder
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies
Properdin deficiency
Proteasome-associated autoinflammatory syndrome
Psoriasis-related juvenile idiopathic arthritis
Pulmonary alveolar microlithiasis
Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome
Pulmonary interstitial glycogenosis
Pulmonary nodular lymphoid hyperplasia
Purine nucleoside phosphorylase deficiency
Pyogenic autoinflammatory syndrome of childhood
RAS-associated autoimmune leukoproliferative disease
Rare pediatric systemic disease
Rare pediatric vasculitis
Rare systemic or rheumatological disease of childhood
Reactive arthritis
Recurrent Neisseria infections due to factor D deficiency
Recurrent infection due to specific granule deficiency
Recurrent infections associated with rare immunoglobulin isotypes deficiency
Recurrent respiratory papillomatosis
Relapsing polychondritis
Respiratory bronchiolitis-interstitial lung disease syndrome
Reticular dysgenesis
Rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies
Rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies
Rheumatoid factor-negative polyarticular juvenile idiopathic arthritis
Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis
Roifman syndrome
Sarcoidosis
Say-Barber-Miller syndrome
Schimke immuno-osseous dysplasia
Secondary interstitial lung disease in childhood and adulthood
Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease
Secondary interstitial lung disease in childhood and adulthood associated with a metabolic disease
Secondary interstitial lung disease in childhood and adulthood associated with a systemic disease
Secondary interstitial lung disease in childhood and adulthood associated with a systemic vasculitis
Secondary interstitial lung disease specific to adulthood associated with a systemic disease
Secondary interstitial lung disease specific to childhood associated with a connective tissue disease
Secondary interstitial lung disease specific to childhood associated with a granulomatous disease
Secondary interstitial lung disease specific to childhood associated with a metabolic disease
Secondary interstitial lung disease specific to childhood associated with a systemic disease
Secondary interstitial lung disease specific to childhood associated with a systemic vasculitis
Secondary pulmonary hemosiderosis
Selective IgM deficiency
Severe acute respiratory syndrome
Severe combined immunodeficiency
Severe combined immunodeficiency due to CORO1A deficiency
Severe combined immunodeficiency due to DCLRE1C deficiency
Severe combined immunodeficiency due to DNA-PKcs deficiency
Severe combined immunodeficiency due to FOXN1 deficiency
Severe combined immunodeficiency due to LCK deficiency
Severe combined immunodeficiency due to adenosine deaminase deficiency
Severe combined immunodeficiency due to complete RAG1/2 deficiency
Severe congenital neutropenia
Severe dermatitis-multiple allergies-metabolic wasting syndrome
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Short-limb skeletal dysplasia with severe combined immunodeficiency
Shwachman-Diamond syndrome
Siegler-Brewer-Carey syndrome
Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells
Spondyloenchondrodysplasia
Staphylococcal necrotizing pneumonia
Sterile multifocal osteomyelitis with periostitis and pustulosis
Sudden infant death-dysgenesis of the testes syndrome
Susceptibility to infection due to TYK2 deficiency
Susceptibility to respiratory infections associated with CD8alpha chain mutation
Susceptibility to viral and mycobacterial infections due to STAT1 deficiency
Sweet syndrome
Syndrome with combined immunodeficiency
Syndromic agammaglobulinemia
Syndromic multisystem autoimmune disease due to Itch deficiency
Systemic-onset juvenile idiopathic arthritis
T-B+ severe combined immunodeficiency
T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta
T-B+ severe combined immunodeficiency due to CD45 deficiency
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
T-B+ severe combined immunodeficiency due to JAK3 deficiency
T-B+ severe combined immunodeficiency due to gamma chain deficiency
T-B- severe combined immunodeficiency
T-cell immunodeficiency with epidermodysplasia verruciformis
T-cell immunodeficiency with thymic aplasia
Takayasu arteritis
Tracheobronchopathia osteochondroplastica
Transient hypogammaglobulinemia of infancy
Tuberculosis
Tumor necrosis factor receptor 1 associated periodic syndrome
Unclassified autoinflammatory syndrome of childhood
Unclassified vasculitis
Unexplained long-lasting fever/inflammatory syndrome
Unexplained periodic fever syndrome of childhood
Unspecified juvenile idiopathic arthritis
Vici syndrome
WHIM syndrome
Wiskott-Aldrich syndrome
X-linked agammaglobulinemia
X-linked hyper-IgM syndrome
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
X-linked immunoneurologic disorder
X-linked lymphoproliferative disease
X-linked mendelian susceptibility to mycobacterial diseases
X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
X-linked severe congenital neutropenia
Yellow nail syndrome
Young syndrome