Chronic Hepatitis C

About the Disease
Hepatitis C, also known as hepatitis c infection, is related to hepatitis c virus and viral infectious disease, and has symptoms including fever, fatigue and loss of appetite. An important gene associated with Hepatitis C is MIR122 (MicroRNA 122), and among its related pathways/superpathways are Innate Immune System and Cytokine Signaling in Immune system. The drugs Ezetimibe and Acarbose have been mentioned in the context of this disorder. Affiliated tissues include Blood, liver and kidney, and related phenotypes are Increased JFH-1 genotype 2a Hepatitis C virus (HCV) infection and immune system

Common Targets
CD24 | IRAK2 | KIR3DS1 | SLC28A2 | SLC28A3 | HLA-DQA1 | GDF15 | PNPLA3 | LOC107986873 | Cyclophilins (nonspecified subtype) | AGT | KIR3DP1 | IFNL3 | G6352 | OAS2 | IL10RA | HLA-A | GALNT8 | HDAC3 | HLA-DQB2 | TNFSF11 | OAS3 | MTHFR | CHODL | TBX21 | HDAC5 | SCARB1 | CCR2 | DPP4 | G1956 | Liver Bile Transporters (LBAT) (nonspecified subtype) | LOC105373723 | VDR | MIR122 | TLR2 | MICB | IL10RB | MASP2 | SERPINE1 | TM6SF2 | CYP24A1 | IFNLR1 | DHX58 | IL1B | SOCS3 | MAVS | AZIN1 | SH3YL1 | CYP2R1 | SLC10A1 | MX1 | CISH | TLR9 | NOS2 | RELL2 | IFNG | MBOAT7 | Caspase (nonspecified subtype) | ATP7B | NADSYN1 | FASLG | MTTP | PLCG1 | LOC105369749 | WTAPP1 | CCR5 | KIR2DL1 | ITPA | KIR2DL5A | GC | MIR146A | IFIH1 | G5970 | UGT1A1 | IL20RA | HLA-DPB1 | HAVCR2 | APOE | FAS | MAPKAPK3 | CXCL10 | KIR2DL2 | HLA-C | HLA-DQB1 | IFNL4 | G7124 | KIR2DP1 | ABCB11 | TGFB1 | DNAAF9 | TLR7 | KIR2DL3 | TAP1 | G7099 | LOC105372379 | IL18 | MMP1 | SLC29A1 | KIR2DS2 | KIR2DL4 | CYP27B1 | IFNAR2 | KIR2DS1 | KIR2DS3 | TAP2 | OPRM1 | KIR2DS4 | IL12B | HDAC2 | RIGI | HLA-DRB1 | OPRK1 | CNR2 | KIR2DS5 | TLR3 | LDLR | HLA-B | METTL1 | KIR3DL1 | TAPBP | DEPDC5 | ART3 | CD209 | HFE | KIR3DL2 | TLR5

Note: If you'd like to get a target analysis report for Chronic Hepatitis C, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Chronic Hepatitis C at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Hypohidrotic Ectodermal Dysplasia, X-linked | Antiphospholipid Syndrome | Branchiootorenal Syndrome | Absence Epilepsy | Glycogen Storage Disease Type 0, Muscle | Dwarfism | Brugada Syndrome 1 | Schizophrenia | Adenoma, Pleomorphic | Epidermodysplasia Verruciformis | Neurofibrosarcoma | Donnai-Barrow Syndrome | Eating Disorder | Dysplastic Nevus | Odonto-onycho-dermal Dysplasia | Methylmalonic Acidemia | Corneal Dystrophy And Perceptive Deafness | Parapsoriasis | Galactosialidosis | Cholesteryl Ester Storage Disease | Uterine Leiomyoma | Mitochondrial Myopathy | X-linked Sideroblastic Anemia | Meningococcal Meningitis | Peyronie's Disease | Hyperacusis | Strabismus | Congenital Afibrinogenemia | Pre-eclampsia | Primary Familial Brain Calcification | Glomerulonephritis, Membranous | Cysticercosis | Hypoalbuminemia | Amish Infantile Epilepsy Syndrome | Paroxysmal Kinesigenic Dyskinesia | Waardenburg Syndrome Type 4 | Chudley-McCullough Syndrome | Mitochondrial Disease | Retinal Vasculitis | Reye Syndrome | Leigh Syndrome | Glycogen Storage Disease Type 3 | Dupuytren Disease | Histiocytosis | Nicotine Addiction | Primary Hyperoxaluria Type 1 | Compartment Syndrome | Chondrosarcoma | Astigmatism | Takotsubo Cardiomyopathy | Orthostatic Intolerance | Light Chain Amyloidosis | Brooke-Spiegler Syndrome | Neonatal Progeroid Syndrome | Spinocerebellar Ataxia Type 10 | Acute Myeloid Leukemia | Albinism | Ocular Surface Squamous Neoplasia | Scleritis | Japanese Encephalitis | Neurocutaneous Melanocytosis | Loeys-Dietz Syndrome Type 4 | High Molecular Weight Kininogen Deficiency | Cushing Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Cholelithiasis | Batten Disease | Basal Ganglia Disease, Biotin-responsive | Multisystemic Smooth Muscle Dysfunction Syndrome | Keratopathy | Deafness, Dystonia, And Cerebral Hypomyelination | Jawad Syndrome | Neuroma | Leber Congenital Amaurosis | Amyotrophic Lateral Sclerosis, Juvenile | Farber Disease | Hypocalcemia | Aneurysm, Abdominal Aortic | Alopecia Areata | Ligneous Conjunctivitis | Acrodermatitis | Waardenburg Syndrome Type 1 | Glycogen Storage Disease Type 1a | Progressive Familial Intrahepatic Cholestasis | Tenosynovial Giant Cell Tumor | Alopecia | Gilbert Syndrome | Iron Overload | Bare Lymphocyte Syndrome | Tay-Sachs Disease | Long QT Syndrome Type 3 | Contact Dermatitis | Otitis Media | Hemochromatosis | Congenital Muscular Dystrophy | Lymphoma | Schizophrenia, Paranoid | Short-chain Acyl-CoA Dehydrogenase Deficiency | Multicentric Carpotarsal Osteolysis Syndrome | Paraganglioma | Neuromuscular Disorders | Dementia, Vascular | Hyperinsulinemia | Muscle Wasting | Episodic Ataxia Type 2 | Dermatitis | Cancer, Kidney | Peters-plus Syndrome | Hemimegalencephaly | Sarcoma, Alveolar Soft Part | Ichthyosis, X-linked | Cerebrovascular Disorders | Charcot-Marie-Tooth Disease, Type 1A | Ehlers-Danlos Syndrome | Fukuyama Congenital Muscular Dystrophy | GM2-gangliosidosis AB Variant | Chondrodysplasia Punctata 1, X-linked Recessive | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Small Lymphocytic Lymphoma | Richter's Syndrome | Steel Syndrome | Brachydactyly | Overactive Bladder | Prurigo Nodularis | Delayed Sleep Phase Syndrome | Skin Papilloma | Cranioectodermal Dysplasia | Vitreoretinopathy, Proliferative | Palmoplantar Keratoderma | Moyamoya Disease | Autoimmune Disease | Eczema | Pituitary Dwarfism | Sporadic Inclusion Body Myositis | Stickler Syndrome | Ganglioneuroma | Nail-Patella Syndrome | Wieacker-Wolff Syndrome | Skin Carcinoma | Neurofibromatosis Type 2 | Atrial Septal Defect | Silicosis | Glycogen Storage Disease Type 0 | Sulfite Oxidase Deficiency | Noonan Syndrome | Extramammary Paget's Disease | X-linked Charcot-Marie-Tooth Disease | Hyperbilirubinemia | Milk Allergy | Hyperoxaluria | Beckwith-Wiedemann Syndrome | Imerslund-Grasbeck Syndrome | Chromosome 5q Deletion Syndrome | Facioscapulohumeral Muscular Dystrophy Type 2 | Biotinidase Deficiency | Benign Hereditary Chorea | Keratitis | Gnathodiaphyseal Dysplasia | Charcot-Marie-Tooth Disease Type 4B1 | Ebstein Anomaly | Osteosarcoma | Adenomyosis | Amebiasis | Renal Oncocytoma | Miyoshi Myopathy | Thyroid Dysgenesis | Chylomicron Retention Disease | Pneumococcal Meningitis | Myasthenia Gravis | Lymphopenia | Beare-Stevenson Syndrome | Pupil Disorders | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Nance-Horan Syndrome | Acute Lymphocytic Leukemia | Multiple Sclerosis, Primary Progressive | Hypertelorism | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Coffin-Siris Syndrome | Endometriosis | Spondylo-ocular Syndrome | Insulinoma | Dystonia-parkinsonism, X-linked | Peutz-Jeghers Syndrome | Primary Torsion Dystonia | Cyst | Dermatofibrosarcoma | Nephrotic Syndrome Type 1 | Hypophosphatasia | Cervicitis | Spondylocarpotarsal Synostosis Syndrome | Costello Syndrome | Danon Disease | Ectodermal Dysplasia | Majeed Syndrome | Meningioma | Hyper IgE Syndrome | Glucagonoma | Depression | Shwachman-Bodian-Diamond Syndrome | Viral Meningitis | Early Infantile Epileptic Encephalopathy 1 | Vertigo | Angioedema | Bulimia Nervosa | Duane Retraction Syndrome | Turner's Syndrome | Psoriasis | Pseudohypoparathyroidism Type 1C | Hypertension, Renovascular | Kabuki Syndrome | Chronic Mucocutaneous Candidiasis | Growth Hormone Excess | Woodhouse-Sakati Syndrome | Hypotrichosis Simplex | Guttate Psoriasis | Encephalopathy, Hepatic | Lipid Metabolism Disorders | Glutaric Aciduria Type 1 | Sweet Syndrome | Osteosclerosis | Pseudohypoparathyroidism Type 1A | Tyrosinemia Type 1 | Preaxial Polydactyly | Osteogenesis Imperfecta Type VI | Leukocyte Adhesion Deficiency | Epidermal Nevus Syndrome | Spinal Muscular Atrophy | Goiter | Chloridorrhea, Congenital | Arts Syndrome | Epicondylitis | Patent Foramen Ovale | Intracerebral Hemorrhage | Schwannomatosis | Hypermetropia | Lennox-Gastaut Syndrome | Stroke, Ischemic | Lesch-Nyhan Syndrome | Fibrodysplasia Ossificans Progressiva | Sarcoma, Ewing | Crigler-Najjar Syndrome | Adenosine Deaminase 2 Deficiency | Chordoid Glioma | Vitamin D Deficiency | Aarskog-Scott Syndrome | Anorchia | Spinal Muscular Atrophy Type 3 | Early Infantile Epileptic Encephalopathy 28 | Argininosuccinic Aciduria | Idiopathic Pulmonary Fibrosis | Myocardial Infarction | Hidradenitis Suppurativa | PHARC Syndrome | Myasthenia | Acute Kidney Injury | Congenital Myasthenic Syndrome | Early Infantile Epileptic Encephalopathy 4 | Epidermolysis Bullosa | Asthma, Nocturnal | Nager Acrofacial Dysostosis | AIDS | Adams-Oliver Syndrome | Frank-ter Haar Syndrome | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Neuromyelitis Optica | Globozoospermia | Leishmaniasis, Cutaneous | Malignant Peripheral Nerve Sheath Tumor | Nephropathy | Reflex Epilepsy | Vasculitis | Microphthalmia | Bainbridge-Ropers Syndrome | Meleda Disease | Heart Failure | Necrobiosis Lipoidica | Urea Cycle Disorder | Rotor Syndrome | Paracoccidioidomycosis | Persistent Fetal Circulation | H Syndrome | Retinal Detachment | Congenital Nephrotic Syndrome | Mast Cell Leukemia | Tricho-hepato-enteric Syndrome | Microtia | Progressive Encephalopathy-optic Atrophy Syndrome | Combined Pituitary Hormone Deficiency | Myotonia | Chondrodysplasia Punctata | Schizoaffective Disorder | Chromosome 16p11.2 Deletion Syndrome | Alazami Syndrome | Carcinoma, Signet Ring Cell | Sialidosis Type I | Pilomatrix Carcinoma | Hyperferritinemia-cataract Syndrome | C3 Glomerulopathy | Giant Cell Arteritis | Atelosteogenesis Type 1 | Diabetic Neuropathy | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Communication Disorders | X-linked Creatine Transporter Deficiency | Relapsing Polychondritis | Retinal Dystrophy, Early-onset Severe | Nestor-Guillermo Progeria Syndrome | Tuberculosis | Lactose Intolerance | Smoldering Myeloma | Scapuloperoneal Myopathy, X-linked Dominant | Connective Tissue Disorders | Sickle Cell Disease | Usher Syndrome Type III | Tuberculous Meningitis | Pain | Sarcoidosis | Common Cold | Carcinoma, Transitional Cell | Progressive Osseous Heteroplasia | Periodontitis | Poirier-Bienvenu Neurodevelopmental Syndrome | Familial Dysautonomia | Joubert Syndrome | Fowler's Syndrome | Keratoacanthoma | Schaaf-Yang Syndrome | Anencephaly | Spinocerebellar Ataxia Type 31 | Ulcerative Colitis | Fascioliasis | Long QT Syndrome Type 1 | Anosmia, Congenital | Micro Syndrome | Osteopathia Striata With Cranial Sclerosis | Carney-Stratakis Syndrome | Sarcomatoid Carcinoma Of The Lung | Fibrosarcoma | Norrie Disease | Non-Langerhans Cell Histiocytosis | Retinal Telangiectasia | Juvenile Myelomonocytic Leukemia | Uveitis | Cleidocranial Dysplasia | Impulse Control Disorder | Scapuloperoneal Spinal Muscular Atrophy | Hypertension, Portal | Spinocerebellar Ataxia Type 38 | Early Infantile Epileptic Encephalopathy 13 | Pseudohypoaldosteronism | Cryptosporidiosis | Carbamoyl Phosphate Synthetase I Deficiency | Sturge-Weber Syndrome | Acrodysostosis | Hemoglobinopathies | Hyperekplexia | Diabetic Nephropathy | HUPRA Syndrome | Shprintzen-Goldberg Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Pneumothorax | Paroxysmal Nocturnal Hemoglobinuria | Familial Isolated Hyperparathyroidism | Mumps | Charcot-Marie-Tooth Disease Type 2D | Osteoarthritis | Tularemia | Wolman Disease | Erythropoietic Protoporphyria | Facioscapulohumeral Muscular Dystrophy Type 1 | Methylmalonic Aciduria And Homocystinuria, CblC Type | Central Pain Syndrome | Niemann-Pick Disease, Type C | Craniopharyngioma | Micropenis | N-acetylglutamate Synthase Deficiency | Spina Bifida | Vitreoretinal Degeneration, Snowflake Type | Leishmaniasis, Visceral | Charcot-Marie-Tooth Disease, Type 6 | Osteogenesis Imperfecta Type I | Temtamy Preaxial Brachydactyly Syndrome | Krabbe Disease | Metachromatic Leukodystrophy | Myositis, Focal | Cri-du-chat Syndrome | Hypercalciuria | Paraplegia | Sarcoidosis, Pulmonary | Familial Cerebral Amyloid Angiopathy | Trichothiodystrophy | Renal Tubular Dysgenesis | Graves Disease | Acute Anterior Uveitis | Congenital Hereditary Endothelial Dystrophy Type II | Endophthalmitis | Amenorrhea