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Nume Hepatitis C Virus
Pagina Web www.malacards.org
Clasificare globală Malacards Genetic diseases; Infectious diseases; Rare diseases
Clasificare anatomică Malacards Gastrointestinal diseases; Immune diseases; Liver diseases
Boli din aceeaşi familie Autoimmune Hepatitis; Hepatitis a; Hepatitis B; Hepatitis C; Hepatitis D; Hepatitis E; Viral Hepatitis

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Boli A-Z Acquired Amegakaryocytic Thrombocytopenia Acquired Hemophilia Acquired Hemophilia a Acquired Immunodeficiency Syndrome Acute Disseminated Encephalomyelitis Acute Liver Failure Acute Transverse Myelitis Adenomatoid Tumor Aging Al Amyloidosis Alcoholic Hepatitis Alcoholic Liver Cirrhosis Alopecia Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alopecia Universalis Congenita Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Amyloidosis Anaplastic Large Cell Lymphoma Aniridia 1 Anorexia Nervosa 1 Antiphospholipid Syndrome Aortitis Aphthous Stomatitis Aplastic Anemia Arteries, Anomalies of Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthropathy Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autoimmune Disease Autoimmune Hepatitis Autoimmune Lymphoproliferative Syndrome, Type V Autoimmune Polyendocrine Syndrome Autonomic Dysfunction Back Pain B-Cell Lymphomas Beta-Thalassemia Biliary Atresia 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 Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Small Vessel Disease with or Without Ocular Anomalies Bronchiolitis Bursitis Buruli Ulcer Carotid Artery Disease Cataract 40 Cataract Congenital Dominant Non Nuclear Cataract, Total Congenital Central Nervous System Lymphoma Central Nervous System Vasculitis Cerebritis Cerebrovascular Disease Chanarin-Dorfman Syndrome Chlamydia Cholangiocarcinoma Cholangiolocellular Carcinoma Cholestasis Chromosomal Triplication Chronic Enteropathy Associated with Slco2a1 Gene Chronic Inflammatory Demyelinating Polyneuropathy Churg-Strauss Syndrome Cocaine Intoxication Cohen-Gibson Syndrome Cold Urticaria Common Variable Immunodeficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Cryoglobulinemia Cryoglobulinemia, Familial Mixed Cryptococcosis Cryptogenic Cirrhosis Cutaneous Polyarteritis Nodosa Cytochrome P450 2d6 Variant Cytomegalovirus Infection Demyelinating Polyneuropathy Dengue Virus Dermatitis Dermatomyositis Desquamative Interstitial Pneumonia Diabetes Mellitus Diarrhea Diffuse Large B-Cell Lymphoma Dilated Cardiomyopathy Discoid Lupus Erythematosus Disseminated Intravascular Coagulation Down Syndrome Duane Retraction Syndrome 1 Eczema Herpeticum Encephalitis Encephalopathy Endocarditis Endotheliitis Eosinophilic Pustular Folliculitis Epidermolytic Hyperkeratosis Epidural Abscess Epithelial Recurrent Erosion Dystrophy Erythema Multiforme Familial Adenomatous Polyposis 1 Fanconi Anemia, Complementation Group E Far Eastern Spotted Fever Fascioliasis Fatty Liver Disease Fibular Hypoplasia and Complex Brachydactyly Focal Segmental Glomerulosclerosis Follicular Lymphoma Folliculitis Foot Drop Friedreich Ataxia 1 Fulminant Viral Hepatitis Fundus Albipunctatus Galactose Epimerase Deficiency Gallbladder Disease Gastritis Gingivitis Glomerulonephritis Glucose Metabolism Disease Glucose Transporter Type 1 Deficiency Syndrome Granuloma Annulare Graves' Disease Guillain-Barre Syndrome, Familial Hansen's Disease Helicobacter Pylori Infection Helix Syndrome Hemihyperplasia, Isolated Hemoglobinopathy Hemoglobinuria Hemolytic Anemia Hemophilia Hemophilia a Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Hepatitis a Hepatitis B Hepatitis C Hepatitis D Hepatitis E Hepatoblastoma Hepatocellular Carcinoma Hepatopulmonary Syndrome Hepatorenal Syndrome Heroin Dependence Herpes Zoster Homocysteinemia Human Coronavirus Sensitivity Human Herpesvirus 8 Human T-Cell Leukemia Virus Type 1 Hyperalphalipoproteinemia 1 Hypercholesterolemia, Autosomal Dominant, Type B Hypersplenism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrophic Cardiomyopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypochondroplasia Hypoglycemia Hypophosphatasia, Adult Hypophosphatasia, Infantile Hypophosphatemia Hypoxia Ichthyosis, Congenital, Autosomal Recessive 11 Immune-Complex Glomerulonephritis Immunoglobulin Alpha Deficiency Inclusion Body Myositis Influenza Insulin-Like Growth Factor I Intrahepatic Cholangiocarcinoma Intrahepatic Cholestasis Ischemia Ischemic Optic Neuropathy Japanese Encephalitis Kaposi Sarcoma Kidney Cancer Klatskin's Tumor Lactic Acidosis Large Granular Lymphocyte Leukemia Laryngeal Cleft Leiomyosarcoma Leukemia Leukodystrophy, Hypomyelinating, 5 Leukoplakia Lewis-Sumner Syndrome Lichen Planus Lichen Planus Pigmentosus Lichen Sclerosus Light Chain Deposition Disease Linear Lichen Planus Linitis Plastica Lipoid Congenital Adrenal Hyperplasia Lipomatosis, Multiple Lissencephaly 1 Liver Cirrhosis Liver Disease Liver Sarcoma Lung Disease Lupus Erythematosus Lymphoma Macroglobulinemia Marginal Zone B-Cell Lymphoma Measles Melanoma Membranoproliferative Glomerulonephritis Membranous Nephropathy Meningitis Meningococcemia Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1 Mesangial Proliferative Glomerulonephritis Mevalonic Aciduria Mixed Cryoglobulinemia Type Iii Monoclonal Gammopathy of Uncertain Significance Mononeuropathy Multiple Mitochondrial Dysfunctions Syndrome 5 Multiple Sclerosis Myelitis Myopathy Myositis Nephrotic Syndrome Neuroblastoma Neuropathy Neuroretinitis Neutropenia Neutrophil Actin Dysfunction Newcastle Disease Nodal Marginal Zone B-Cell Lymphoma Nonalcoholic Steatohepatitis Noonan Syndrome 1 Noonan Syndrome 2 Noonan Syndrome 3 Opiate Dependence Oral Erosive Lichen Oral Leukoplakia Oral Lichen Planus Osteomyelitis Osteoporotic Fracture Palmoplantar Carcinoma, Multiple Self-Healing Pancreatitis Papilloma Parkinson Disease 2, Autosomal Recessive Juvenile Pediatric Lymphoma Pemphigus Pemphigus Foliaceus Peptic Ulcer Disease Periodontitis, Aggressive, 1 Peritonitis Persistent Idiopathic Facial Pain Pityriasis Rosea Plasmablastic Lymphoma Plasma Cell Leukemia Pneumonia Polyarteritis Nodosa Polycythemia Polycythemia Vera Polykaryocytosis Inducer Polymyositis Polyneuropathy Porokeratosis Porphyria Porphyria Cutanea Tarda Porphyria Cutanea Tarda, Type I Portal Hypertension Portal Vein Thrombosis Primary Biliary Cirrhosis Primary Central Nervous System Lymphoma Primary Cutaneous Anaplastic Large Cell Lymphoma Primary Effusion Lymphoma Progressive Multifocal Leukoencephalopathy Proliferative Glomerulonephritis Pseudobulbar Affect Psoriasis Psoriasis 13 Psoriatic Arthritis Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 Pulmonary Tuberculosis Pure Red-Cell Aplasia Purpura Pustular Psoriasis Pyoderma Pyoderma Gangrenosum Pyruvate Carboxylase Deficiency Radin Blood Group Antigen Ramer Ladda Syndrome Rapidly Progressive Glomerulonephritis Reactive Arthritis Relapsing Polychondritis Renal Hypodysplasia/aplasia 1 Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinal Vasculitis Retinitis Retinoblastoma Rheumatic Disease Rheumatoid Arthritis Rheumatoid Nodulosis Roberts Syndrome Sarcoidosis 2 Sarcoma Satb2-Associated Syndrome Scalp-Ear-Nipple Syndrome Schistosomiasis Schizophrenia Scleritis Scleromyxedema Scotoma Septic Arthritis Severe Acute Respiratory Syndrome Sialadenitis Sickle Cell Anemia Singleton-Merten Syndrome Sjogren Syndrome Skin Disease Skin Sarcoidosis Sleeping Sickness Spasticity Spastic Paraparesis Spindle Cell Hemangioma Splenic Marginal Zone Lymphoma Splenomegaly Squamous Cell Carcinoma Stomatitis Subacute Thyroiditis Substance Abuse Suppressor of Tumorigenicity 3 Synovitis Syphilis T-Cell Leukemia Temporal Arteritis Tertiary Syphilis Tetanus Thalassemia Thrombocytopenia Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Transmitted_by Transverse Myelitis Trypanosomiasis, Human East-African Tuberous Sclerosis Tumefactive Multiple Sclerosis Type Ii Mixed Cryoglobulinemia Urinary Schistosomiasis Urticaria Uveitis Vaccinia Valproate Embryopathy Van Der Woude Syndrome 1 Varicose Veins Vasculitis Viral Hepatitis Viral Infectious Disease Virus Associated Hemophagocytic Syndrome Vogt-Koyanagi-Harada Disease West Nile Virus Yellow Fever Zinc-Responsive Necrolytic Acral Erythema