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Nume Cystic Fibrosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Cystic fibrosis with intestinal manifestations; Cystic fibrosis with other manifestations; Cystic fibrosis with pulmonary manifestations; Cystic fibrosis, unspecified
Clasificare anatomică Malacards Boli ale sistemului reproducator; Boli endocrine; Boli gastrointestinale; Boli hepatice; Boli respiratorii

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Boli A-Z 46,xy Gonadal Dysgenesis, Partial, with Minifascicular Neuropathy Acalculous Cholecystitis Acardia Achalasia-Addisonianism-Alacrima Syndrome Acrocallosal Syndrome Acrodermatitis Acute Insulin Response Acute Leukemia of Ambiguous Lineage Acute Pancreatitis Acute Respiratory Distress Syndrome Adenocarcinoma Adie Pupil Agammaglobulinemia Aggressive Periodontitis Aging Alcoholic Pancreatitis Allergic Bronchopulmonary Aspergillosis Allergic Bronchopulmonary Aspergillosis, Familial Allergic Rhinitis Alobar Holoprosencephaly Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-1-Antitrypsin Deficiency Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amyloidosis Anauxetic Dysplasia 1 Anca-Associated Vasculitis Androgen Insensitivity Syndrome, Mild Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Aortic Atherosclerosis Apparent Mineralocorticoid Excess Appendicitis Aquagenic Syringeal Acrokeratoderm Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Asperger Syndrome Aspergillosis Asthma Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Telangiectasia Autoimmune Pancreatitis Autonomic Dysfunction Autosomal Dominant Polycystic Kidney Disease Autosomal Recessive Disease Azoospermia Bacterial Vaginosis Beckwith-Wiedemann Syndrome Beta-Lactam Allergy Beta-Thalassemia Bile Duct Disease Bile Reflux Biliary Atresia Biliary Tract Disease Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Breast Cancer Bronchial Disease Bronchiectasis Bronchiectasis with or Without Elevated Sweat Chloride 1 Bronchiectasis with or Without Elevated Sweat Chloride 2 Bronchiectasis with or Without Elevated Sweat Chloride 3 Bronchiolitis Bronchiolitis Obliterans Bronchitis Bronchopneumonia Bronchopulmonary Dysplasia Candidiasis Cardiac Arrest Cardiac Tamponade Cataract Central Retinal Vein Occlusion Cerebritis Cerebrocostomandibular Syndrome Cervical Cancer Cervicitis Cholangitis Cholangitis, Primary Sclerosing Cholecystitis Cholera Cholestasis Chops Syndrome Chronic Fatigue Syndrome Chronic Granulomatous Disease Chronic Maxillary Sinusitis Chronic Ulcer of Skin Cleft Palate with or Without Ankyloglossia, X-Linked Clostridium Difficile Colitis Coffin-Lowry Syndrome Cohen-Gibson Syndrome Colitis Colonic Atresia Colonic Disease Common Cold Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Chloride Diarrhea Congenital Granular Cell Tumor Congenital Hypothyroidism Constipation Croup Crouzon Syndrome with Acanthosis Nigricans Cystadenocarcinoma Cystadenoma Cystathioninuria Cystic Echinococcosis Cystic Fibrosis, Modifier of, 1 Cystic Lymphangioma Cystinosis Dental Caries Dermatitis Diabetes Insipidus Diabetes Mellitus Diaphragmatic Hernia, Congenital Diarrhea Diencephalic Syndrome Duodenal Ulcer Duodenitis Echinococcosis Ectodermal Dysplasia Ehlers-Danlos Syndrome Encephalomyopathy Encephalopathy, Ethylmalonic Endotheliitis Enterokinase Deficiency Enteropathica Eosinophilic Gastroenteritis Epithelial Recurrent Erosion Dystrophy Esophagitis, Eosinophilic, 1 Exocrine Pancreatic Insufficiency Exophthalmos Extrapontine Myelinolysis Exudative Vitreoretinopathy Fanconi Anemia, Complementation Group E Fibrosis of Extraocular Muscles, Congenital, 1 Folliculitis Fragile X Syndrome Galactosemia Gallbladder Disease Gastroduodenitis Gastroesophageal Reflux Gastrointestinal System Disease Gastroparesis Giardioză Gilbert Syndrome Gingivitis Glomerulonephritis Glucose Intolerance Goblet Cell Carcinoid Granulocytopenia Granulomatous Dermatitis Growth Hormone Deficiency Haemophilus Influenzae Headache Associated with Sexual Activity Helix Syndrome Hellp Syndrome Hemiplegic Migraine Hemochromatosis, Neonatal Hemoglobinopathy Hemolytic Anemia Hemophilia Hemophilia B Hemosiderosis Hepatic Adenomas, Familial Hepatitis Hepatitis a Hepatoblastoma Hepatopulmonary Syndrome Hernia, Hiatus Holoprosencephaly Hydrocele Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperaldosteronism, Familial, Type I Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hyperglycemia Hyperparathyroidism Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Pyloric Stenosis Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome Hypervitaminosis a Hypervitaminosis D Hypoglycemia Hypokalemia Hypoxia Idiopathic Bronchiectasis Ige Responsiveness, Atopic Immunoglobulin E Concentration, Serum Infertility Inflammatory Bowel Disease Inflammatory Diarrhea Influenza Inguinal Hernia Inherited Metabolic Disorder Insulin-Like Growth Factor I Intermediate Uveitis Interstitial Lung Disease Intestinal Disease Intestinal Volvulus Intussusception Invasive Aspergillosis Isolated Growth Hormone Deficiency Isolated Optic Neuritis Jejunal Atresia Kartagener Syndrome Keratomalacia Keshan Disease Kindler Syndrome Kwashiorkor Leukemia Liddle Syndrome Lipomatosis Lissencephaly 1 Liver Cirrhosis Liver Disease Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Lung Abscess Lung Cancer Lung Disease Lupus Erythematosus Lymphangioma Lymphoblastic Leukemia Lymphoma Male Infertility Mannose-Binding Lectin Deficiency Maxillary Sinusitis Meconium Ileus Mediastinitis Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency Megacolon Melioidosis Membranoproliferative Glomerulonephritis Middle Ear Disease Mucinous Cystadenocarcinoma Mucinous Cystadenocarcinoma of the Pancreas Mucinous Intrahepatic Cholangiocarcinoma Mucositis Multidrug-Resistant Tuberculosis Multiple Mitochondrial Dysfunctions Syndrome 5 Muscular Atrophy Muscular Dystrophy Mycetoma Mycobacterium Abscessus Mycobacterium Chelonae Mycobacterium Fortuitum Mycobacterium Gordonae Mycobacterium Kansasii Mycobacterium Marinum Myelitis Myotonia Congenita, Autosomal Dominant Nasopharyngitis Neonatal Jaundice Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephrotic Syndrome Neurodegeneration with Brain Iron Accumulation 2a Neurofibromatosis, Type Iv, of Riccardi Neuromuscular Disease Neuronal Intestinal Dysplasia Neuronal Intestinal Dysplasia, Type B Neuronitis Neuropathy Neutrophil Migration Niemann-Pick Disease Night Blindness Nocardiosis Non-Involuting Congenital Hemangioma Nontuberculous Mycobacterial Lung Disease Nutritional Deficiency Disease Otitis Media Ovalocytosis, Southeast Asian Ovarian Cancer Ovarian Hyperstimulation Syndrome Panbronchiolitis, Diffuse Pancreatic Agenesis 1 Pancreatic Cancer Pancreatic Ductal Adenocarcinoma Pancreatic Mucinous Cystadenoma Pancreatitis Pancreatitis, Hereditary Paranasal Sinus Disease Partial Deletion of Y Pericardial Effusion Pericarditis Periodontitis Periodontosis Peritonitis Pertussis Pharyngitis Phenylketonuria Pick Disease of Brain Pituitary Adenoma 1, Multiple Types Plastic Bronchitis Pleural Empyema Pneumonia Pneumothorax Polycystic Kidney Disease Porokeratosis Portal Hypertension Post-Transplant Lymphoproliferative Disease Primary Ciliary Dyskinesia Primary Hyperparathyroidism Prolidase Deficiency Prostate Cancer Prostatitis Pseudohypoaldosteronism Pseudohypoaldosteronism, Type I, Autosomal Dominant Pseudohypoaldosteronism, Type I, Autosomal Recessive Pseudoxanthoma Elasticum Pulmonary Alveolar Microlithiasis Pulmonary Aspergilloma Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Emphysema Pulmonary Fibrosis Pulmonary Fibrosis, Idiopathic Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Sarcoidosis Pyloric Stenosis Pyomyositis Radiation Induced Cancer Rapidly Progressive Glomerulonephritis Recurrent Acute Pancreatitis Renal Glucosuria Respiratory Syncytial Virus Infectious Disease Retinal Vein Occlusion Retinitis Retinitis Pigmentosa 73 Rheumatic Disease Rheumatoid Arthritis Rhinitis Riboflavin Deficiency Sarcoidosis 2 Scedosporiosis Sclerosing Cholangitis Scoliosis Secretory Diarrhea Shwachman-Diamond Syndrome Sialolithiasis Sickle Cell Anemia Sickle Cell Disease Silver-Russell Syndrome Sinusitis Situs Inversus Solar Urticaria Spinal Muscular Atrophy Splenomegaly Spondylocarpotarsal Synostosis Syndrome Squamous Cell Carcinoma Status Asthmaticus Steatorrhea Stenotrophomonas Maltophilia Infection Subdural Empyema Suppurative Cholangitis Surfactant Dysfunction Surfactant Metabolism Dysfunction, Pulmonary, 2 Surfactant Metabolism Dysfunction, Pulmonary, 3 Surfactant Metabolism Dysfunction, Pulmonary, 4 Sveinsson Chorioretinal Atrophy Syndrome of Inappropriate Antidiuretic Hormone Systemic Lupus Erythematosus Tay-Sachs Disease Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thrombophilia Thrombophlebitis Thrombosis Thyroiditis Tracheomalacia Transverse Myelitis Trichomoniasis Tropical Calcific Pancreatitis Turner Syndrome Typhoid Fever Undifferentiated Pleomorphic Sarcoma Urticaria Van Der Woude Syndrome 1 Vasculitis Vas Deferens, Congenital Bilateral Aplasia of Virus-Associated Trichodysplasia Spinulosa Vulvovaginal Candidiasis Vulvovaginitis Wegener Granulomatosis Wilson Disease Wrinkles Xerophthalmia