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Boli A-Z 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 3-Methylglutaconic Aciduria 3-Methylglutaconic Aciduria, Type V Acquired Immunodeficiency Syndrome Acquired Metabolic Disease Acrocallosal Syndrome Acrokeratosis Verruciformis Acromegaly Acute Mountain Sickness Acute Myocardial Infarction Acute Myocarditis Acute Pyelonephritis Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of Adams-Oliver Syndrome Adie Pupil Adult-Onset Still's Disease Aggressive Periodontitis Aging Al Amyloidosis Allergic Contact Dermatitis Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 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 Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity Syndrome, Mild Aneurysm Angina Pectoris Aniridia 1 Anorexia Nervosa 1 Anterolateral Myocardial Infarction Antiphospholipid Syndrome Anuria Aortic Coarctation Aortic Disease Aortic Valve Disease 2 Apert Syndrome Aphthous Stomatitis Apnea, Obstructive Sleep Appendicitis Apraxia Arrhythmogenic Right Ventricular Cardiomyopathy Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Aseptic Meningitis Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Atrial Fibrillation Atrial Heart Septal Defect Atrial Septal Aneurysm Atrial Septal Defect 4 Atrial Standstill Atrial Standstill 1 Atrioventricular Block Atrioventricular Septal Defect Aural Atresia, Congenital Autoimmune Disease Autoimmune Hepatitis Autoimmune Myocarditis Autoinflammation, Lipodystrophy, and Dermatosis Syndrome Autosomal Dominant Polycystic Kidney Disease Autosomal Recessive Limb-Girdle Muscular Dystrophy Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2e Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2f Axonal Neuropathy Bacterial Meningitis Bardet-Biedl Syndrome Barth Syndrome Benign Chronic Pemphigus Beriberi Beryllium Disease 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 Fracture Bone Inflammation Disease Borjeson-Forssman-Lehmann Syndrome Brachydactyly Breast Cancer Bronchiolitis Obliterans Brucellosis Cardiac Arrest Cardiac Conduction Defect Cardiac Conduction Disease with or Without Dilated Cardiomyopathy Cardiac Sarcoidosis Cardiac Valvular Defect, Developmental Cardiogenic Shock Cardiomyopathy Cataract Hip Spine Disease Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 1b Cardiomyopathy, Dilated, 1d Cardiomyopathy, Dilated, 1dd Cardiomyopathy, Dilated, 1e Cardiomyopathy, Dilated, 1o Cardiomyopathy, Dilated, 1x Cardiomyopathy, Dilated, 3b Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma Cardiomyopathy, Familial Hypertrophic, 1 Cardiomyopathy, Familial Hypertrophic, 4 Cardiomyopathy, Familial Restrictive, 1 Cardioneuromyopathy with Hyaline Masses and Nemaline Rods Carnitine Deficiency, Systemic Primary Carotid Artery Disease Carotid Stenosis Cataract Catastrophic Antiphospholipid Syndrome Catecholaminergic Polymorphic Ventricular Tachycardia Celiac Disease 1 Central Nervous System Vasculitis Central Sleep Apnea Centronuclear Myopathy Cerebellofaciodental Syndrome Cerebritis Cervicitis Chagas Disease Chlamydia Cholangitis Cholestasis Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioamnionitis Chronic Fatigue Syndrome Churg-Strauss Syndrome Chylothorax, Congenital Clonorchiasis Cocaine Abuse Colitis Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Complex Regional Pain Syndrome Conduct Disorder Congenital Cytomegalovirus Congenital Disorder of Glycosylation, Type Ic Congenital Disorder of Glycosylation, Type Im Congenital Fiber-Type Disproportion Congenital Generalized Lipodystrophy Congestive Heart Failure Conjunctivitis Conjunctivochalasis Connective Tissue Disease Contact Dermatitis Corneal Dystrophy, Fleck Coronary Artery Anomaly Coronary Stenosis Cor Triatriatum Creatine Phosphokinase, Elevated Serum Crouzon Syndrome with Acanthosis Nigricans Cystic Echinococcosis Cytomegalovirus Infection Danon Disease Darier-White Disease Dengue Hemorrhagic Fever Denys-Drash Syndrome Diabetic Foot Ulcers Diarrhea Diastolic Heart Failure Diffuse Cutaneous Mastocytosis Digeorge Syndrome Dirofilariasis Distal Arthrogryposis Double-Orifice Mitral Valve Dystrophinopathies Eales Disease Eating Disorder Ebstein Anomaly Echinococcosis Ectodermal Dysplasia Ectodermal Dysplasia/skin Fragility Syndrome Ehlers-Danlos Syndrome Emerinopathy Emery-Dreifuss Muscular Dystrophy Encephalopathy Endocardial Fibroelastosis Endocarditis Endometritis Endomyocardial Fibroelastosis Endomyocardial Fibrosis Endotheliitis End Stage Renal Failure Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica Epidermolysis Bullosa, Lethal Acantholytic Epidermolysis Bullosa Simplex Epidermolysis Bullosa Simplex with Muscular Dystrophy Epilepsy Epiphyseal Dysplasia, Multiple, 1 Epithelial Recurrent Erosion Dystrophy Epithelioid Neurofibroma Essential Thrombocythemia Extracardiac Rhabdomyoma Extrinsic Allergic Alveolitis Extrinsic Cardiomyopathy Fainting Familial Hypertension Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form Familial Isolated Dilated Cardiomyopathy Familial Isolated Restrictive Cardiomyopathy Familial Long Qt Syndrome Familial Partial Lipodystrophy Familial Sick Sinus Syndrome Fascioliasis Fetal Akinesia Deformation Sequence Fibromuscular Dysplasia Fukuyama Type Muscular Dystrophy Ganglioneuroblastoma Gapo Syndrome Gastroenteritis Giant Cell Myocarditis Gingival Disease Gingival Fibromatosis Gingival Overgrowth Gingivitis Gitelman Syndrome Glucagonoma Glucose Metabolism Disease Glucose Transporter Type 1 Deficiency Syndrome Gout Graft-Versus-Host Disease Griscelli Syndrome Grover's Disease Growth Hormone Deficiency Heart Conduction Disease Heart Disease Heart Tumor Heart Valve Disease Hemihyperplasia, Isolated Hemolytic-Uremic Syndrome Hemophagocytic Lymphohistiocytosis, Familial, 2 Hemorrhagic Fever Hemorrhagic Fever with Renal Syndrome Hemosiderosis Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis C Hepatitis C Virus Hepatopulmonary Syndrome Hepatorenal Syndrome Heterotaxy Hidradenitis Hidradenitis Suppurativa Hinman Syndrome Holt-Oram Syndrome Hyaline Fibromatosis Syndrome Hydrolethalus Syndrome 1 Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypercholesterolemia, Autosomal Dominant, 3 Hypereosinophilic Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hyperthyroidism Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoaldosteronism Hypogonadism Hypoparathyroidism Hypopituitarism Hypoplastic Left Heart Syndrome Hyporeninemic Hypoaldosteronism Hypoxia Ichthyosis, Congenital, Autosomal Recessive 11 Ichthyosis Prematurity Syndrome Idiopathic Hypercalciuria Idiopathic Neutropenia Iga Glomerulonephritis Immunodeficiency 43 Immunoglobulin E Concentration, Serum Inclusion Body Myositis Infectious Myocarditis Inguinal Hernia Intermittent Claudication Interstitial Nephritis Intrahepatic Cholestasis Intrinsic Cardiomyopathy Ischemia Ischemic Heart Disease Ischemic Optic Neuropathy Isolated Hyperckemia Joint Disorders Juvenile Myasthenia Gravis Juvenile Rheumatoid Arthritis Kashin-Beck Disease Kawasaki Disease Kearns-Sayre Syndrome Keratoconjunctivitis Sicca Keratoderma with Woolly Hair Keratosis Keshan Disease Laryngitis Left Ventricular Noncompaction Leptospirosis Levocardia Limb-Girdle Muscular Dystrophy Limbic Encephalitis with Lgi1 Antibodies Limb Ischemia Lipid Storage Disease Lipodystrophy Liver Cirrhosis Lmna-Related Dilated Cardiomyopathy Localized Scleroderma Loeys-Dietz Syndrome Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Long Qt Syndrome Long Qt Syndrome 6 Lung Squamous Cell Carcinoma Lupus Erythematosus Lyme Disease Lymph Node Disease Macular Dystrophy, Retinal, 1, North Carolina Type Major Affective Disorder 2 Malignant Hypertension Malignant Hyperthermia Marfan Syndrome Mcleod Syndrome Mediastinitis Meningitis Meningococcal Infection Microcolon Microscopic Colitis Microvascular Complications of Diabetes 3 Microvascular Complications of Diabetes 5 Migraine with or Without Aura 1 Miliary Tuberculosis Mitochondrial Disorders Mitral Valve Disease Mixed Connective Tissue Disease Mohr-Tranebjaerg Syndrome Mucolipidosis Ii Alpha/beta Mucolipidosis Iv Mucopolysaccharidosis-Plus Syndrome Multiple Endocrine Neoplasia Mungan Syndrome Muscle Eye Brain Disease Muscle Hypertrophy Muscle Tissue Disease Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital, Lmna-Related Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Duchenne and Becker Type Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy , Type a, 4 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 Muscular Dystrophy, Limb-Girdle, Type 2a Muscular Dystrophy, Limb-Girdle, Type 2b Muscular Dystrophy, Limb-Girdle, Type 2c Muscular Dystrophy, Limb-Girdle, Type 2d Muscular Dystrophy, Limb-Girdle, Type 2f Muscular Dystrophy, Limb-Girdle, Type 2h Muscular Dystrophy, Limb-Girdle, Type 2j Myasthenia Gravis Myocardial Infarction Myocardial Stunning Myocarditis Myofibrillar Myopathy Myopathy Myopathy, Centronuclear, 2 Myopathy, Myofibrillar, 1 Myopathy, Myofibrillar, 2 Myopathy, Spheroid Body Myopathy, X-Linked, with Excessive Autophagy Myosin Storage Myopathy Myositis Myotonia Myotonic Dystrophy Naxos Disease Nemaline Myopathy Neonatal Lupus Erythematosus Nephrogenic Systemic Fibrosis Nephrosclerosis Neuroblastoma Neuropathy Neutropenia Nonarteritic Anterior Ischemic Optic Neuropathy Obsessive-Compulsive Disorder Obstructive Jaundice Oculodentodigital Dysplasia Oliver Syndrome Opportunistic Mycosis Optic Atrophy 3, Autosomal Dominant Orthostatic Intolerance Palmoplantar Keratoderma and Woolly Hair Palmoplantar Keratoderma, Epidermolytic Panuveitis Papillomatosis, Confluent and Reticulated Paraneoplastic Pemphigus Patent Foramen Ovale Pemphigus Vulgaris Pericardial Effusion Pericarditis Perinephritis Periodontal Disease Periodontitis Peripartum Cardiomyopathy Peripheral Artery Disease Peritonitis Phaeochromocytoma Pheochromocytoma Pineal Region Choriocarcinoma Plasmodium Vivax Malaria Pneumoconiosis Pneumonia Portal Hypertension Posterior Urethral Valves Prader-Willi Syndrome Primary Amebic Meningoencephalitis Primary Systemic Mycosis Propionic Acidemia Prostatitis Protein-Energy Malnutrition Psoriasis Psoriasis 13 Pulmonary Aspergilloma Pulmonary Disease, Chronic Obstructive Pulmonary Edema Pulmonary Embolism Pulmonary Hemosiderosis Pulmonary Hypertension Pulmonary Sequestration Pulmonary Tuberculosis Pulpitis Purpura Pustular Psoriasis Pyelonephritis Q Fever Reactive Arthritis Recessive Dystrophic Epidermolysis Bullosa Reducing Body Myopathy Relapsing-Remitting Multiple Sclerosis Renal Artery Disease Renal Fibrosis Renal Hypertension Renal Tuberculosis Renal Tubular Dysgenesis Renovascular Hypertension Respiratory System Disease Resting Heart Rate, Variation in Restrictive Cardiomyopathy Retinitis Rheumatic Disease Rheumatic Heart Disease Rheumatoid Arthritis Rheumatoid Lung Disease Rheumatoid Nodulosis Rheumatoid Vasculitis Rickets Rubella Sarcoidosis 2 Schistosomiasis Schnyder Corneal Dystrophy Scrub Typhus Sensorineural Hearing Loss Severe Combined Immunodeficiency Sheehan Syndrome Short Qt Syndrome Shwachman-Diamond Syndrome Sick Sinus Syndrome Silicosis Silver-Russell Syndrome Sinoatrial Node Disease Sleep Apnea Smallpox Sorsby Fundus Dystrophy Spastic Entropion Spondylitis Spondyloarthropathy Spondyloarthropathy 1 Squamous Cell Carcinoma Squamous Cell Carcinoma of the Hypopharynx Subacute Cerebellar Degeneration Superior Limbic Keratoconjunctivitis Syncope Syndrome of Inappropriate Antidiuretic Hormone Synovitis Systolic Heart Failure Takayasu Arteritis Tendinosis Tetralogy of Fallot Thrombosis Thyroiditis Toxic Shock Syndrome Toxoplasmoză Transverse Myelitis Treacher Collins Syndrome 1 Tropical Endomyocardial Fibrosis Trypanosomiasis Tuberous Sclerosis Turner Syndrome Type Ii Mixed Cryoglobulinemia Typhoid Fever Ulcerative Colitis Uveitis Vascular Disease Vasculitis Ventricular Fibrillation, Paroxysmal Familial, 1 Ventricular Septal Defect Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy Viral Encephalitis Visceral Heterotaxy Vogt-Koyanagi-Harada Disease Walker-Warburg Syndrome Wolff-Parkinson-White Syndrome