Disease

Common Cold

About the Disease
Common Cold, also known as acute nasopharyngitis, is related to cryoglobulinemia and cryoglobulinemia, familial mixed, and has symptoms including coughing, fever and pruritus. An important gene associated with Common Cold is TMEM106B (Transmembrane Protein 106B), and among its related pathways/superpathways are ERK Signaling and Innate Immune System. The drugs Cefditoren and Racephedrine have been mentioned in the context of this disorder. Affiliated tissues include liver, skin and pituitary, and related phenotypes are no effect and no effect

Common Targets
NAT2 | PLAAT4 | NF-kappaB (NFkB) | PLAAT3 | Opioid receptor (nonspecified subtype) | PLAAT2 | SEPTIN9 | CHRM3 | HRH1 | PLAT | alpha1-Adrenoceptor (nonspecified subtype) | RASSF1 | ASIC1 | OPRM1 | Adrenoceptor (nonspecified subtype) | CYP2C19 | G5743 | H4C6 | PLAAT5 | PTGS1 | ADRA1A | CHRM1

疾病靶点研报
Common Cold

Note: If you'd like to get a target analysis report for Common Cold, 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 Common Cold at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Pure Red Cell Aplasia | Familial Hypertrophic Cardiomyopathy | Purpura, Thrombotic Thrombocytopenic | Urolithiasis | Burn-McKeown Syndrome | Depression | Intestinal Hypomagnesemia 1 | Neurofibromatosis Type 1 | Liver Diseases | Smoldering Myeloma | Sclerosteosis 2 | Parvovirus B19 Infection | Early Infantile Epileptic Encephalopathy 4 | Olmsted Syndrome | Nail-Patella Syndrome | Hypotension, Orthostatic | Stroke, Hemorrhagic | Vascular Cognitive Impairment | Congenital Disorders Of Glycosylation Type II | Meleda Disease | Pitt-Hopkins Syndrome | Thrombophilia | Kabuki Syndrome | Eiken Syndrome | Inflammatory Bowel Disease | Choroideremia | Silicosis | Polycystic Kidney, Autosomal Recessive | Gray Platelet Syndrome | Hamartoma | Tyrosinemia Type 1 | Facioscapulohumeral Muscular Dystrophy | Cholangiocarcinoma | Klinefelter Syndrome | Myelitis, Transverse | Skin Papilloma | Hydronephrosis | Alpha-mannosidosis | Multiple System Atrophy | Acquired Partial Lipodystrophy | Focal Cortical Dysplasia Type 2 | Triple A Syndrome | Cramp Fasciculation Syndrome | Muckle-Wells Syndrome | Acne | Spinal Muscular Atrophy Type 2 | Inflammatory Linear Verrucous Epidermal Nevus | Spinal Muscular Atrophy | Meningococcal Meningitis | Generalized Epilepsy And Paroxysmal Dyskinesia | Acromesomelic Dysplasia | Hyperparathyroidism | Spondyloarthritis | Sandhoff Disease | Kabuki Syndrome 2 | Kindler Syndrome | REM Sleep Behavior Disorder | Waardenburg Syndrome Type 1 | Carbonic Anhydrase VA Deficiency | Miyoshi Myopathy | Epidermal Nevus Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Leishmaniasis, Cutaneous | Spinocerebellar Ataxia Type 7 | Filariasis | Learning Disability | Hereditary Spherocytosis | Martsolf Syndrome | CDKL5 Deficiency Disorder | Juvenile Myelomonocytic Leukemia | Retinal Dystrophy | Lymphomatoid Granulomatosis | Hypoglycemia | Primary Lateral Sclerosis | Empyema | Cerebral Amyloid Angiopathy | Transient Bullous Dermolysis Of The Newborn | Cancer, Kidney | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Vulvovaginitis | Intestinal Tuberculosis | Dysfibrinogenemia | Anorchia | Dysthymia | Isobutyryl-CoA Dehydrogenase Deficiency | Dominant Optic Atrophy | Tetanus | Spinocerebellar Ataxia | Neuromuscular Disorders | Spinal Muscular Atrophy Type 3 | Spinocerebellar Ataxia Type 6 | Hypodontia | Congenital Dyserythropoietic Anemia Type 4 | Primary Hyperoxaluria Type 3 | Schwannomatosis | Spinocerebellar Ataxia Type 5 | Acute Coronary Syndrome | Vitreoretinal Degeneration, Snowflake Type | Heart Failure | Wagner Disease | Myelomeningocele | Leukocyte Adhesion Deficiency | Keratoconjunctivitis | Corneal Dystrophy And Perceptive Deafness | Familial Episodic Pain Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Alcoholism | Cholestasis, Intrahepatic | Saul-Wilson Syndrome | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Johanson-Blizzard Syndrome | Megalencephaly | Epidermolysis Bullosa Simplex, Generalized | Meconium Ileus | T-cell Lymphoma, Subcutaneous Panniculitis-like | Polyomavirus Nephropathy | Cardiospondylocarpofacial Syndrome | Encephalopathy | Gangliosidosis, GM1 | Spondylometaphyseal Dysplasia | Fukuyama Congenital Muscular Dystrophy | Porphyria Cutanea Tarda | Rhizomelic Chondrodysplasia Punctata | Hypertelorism | Encephalopathy, Glycine | Retinopathy Of Prematurity | Stromal Corneal Dystrophy | Uveitis, Anterior | Castleman Disease | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Joubert Syndrome | Atopic Dermatitis | Vitamin D Deficiency | Familial Retinal Arterial Macroaneurysm | Ocular Hypertension | Hemangioblastoma | Chiari Malformation Type I | Focal Segmental Glomerulosclerosis | Histiocytosis | Iron Deficiency Anemia | AIDS | Gigantism | Hypertension | Cardiomyopathy, Peripartum | Senior-Loken Syndrome | Turner's Syndrome | Hyperferritinemia-cataract Syndrome | Protein C Deficiency | Ligneous Conjunctivitis | Insulin Resistance | Dystonia | DEND Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Hyperandrogenemia | Atherosclerosis | Behcet's Disease | Ophthalmia, Sympathetic | Biotinidase Deficiency | Pontocerebellar Hypoplasia Type 7 | X-linked Sideroblastic Anemia | Babesiosis | Connective Tissue Disorders | Loeys-Dietz Syndrome Type 4 | Cystinuria | Inflammatory Myofibroblastic Tumor | Coronary Heart Disease | Cholelithiasis | Mitochondrial DNA Depletion Syndrome 13 | Scapuloperoneal Spinal Muscular Atrophy | Aphasia | Skin Fragility-woolly Hair Syndrome | Meningioma | GAPO Syndrome | Lattice Corneal Dystrophy | Impulse Control Disorder | Mucormycosis | Meniere's Disease | Sarcoma | Atrial Septal Defect | Oculopharyngeal Muscular Dystrophy | Trimethylaminuria | Lattice Corneal Dystrophy Type 1 | Obesity | Christianson Syndrome | Ocular Surface Squamous Neoplasia | Hyperekplexia | Periodontitis | Craniopharyngioma | Acute Motor Axonal Neuropathy | Hemophagocytic Lymphohistiocytosis | Osteogenesis Imperfecta Type I | Hypercholesterolemia, Familial | Intermittent Explosive Disorder | Antiphospholipid Syndrome | Exostoses | Cystitis | Binge Eating Disorder | Chondrosarcoma | Uveitis | Calcium Pyrophosphate Deposition Disease | Eosinophilic Asthma | SAPHO Syndrome | Pneumonia, Mycoplasma | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Palmoplantar Keratoderma | Pyruvate Carboxylase Deficiency Disease | Graves Disease | Maternally Inherited Diabetes And Deafness | Dermatitis Herpetiformis | Epidermolysis Bullosa | Mixed Connective Tissue Disease | Epicondylitis | Spondylocarpotarsal Synostosis Syndrome | Cranioectodermal Dysplasia | Hyperhomocysteinemia | Takotsubo Cardiomyopathy | Multiple Epiphyseal Dysplasia | Dysequilibrium Syndrome | Neurocysticercosis | Familial Cerebral Amyloid Angiopathy | Wolcott-Rallison Syndrome | Poretti-Boltshauser Syndrome | Cutis Laxa | Purpura | Obesity, Morbid | Hereditary Mixed Polyposis Syndrome | Stevens-Johnson Syndrome | Congenital Torticollis | Hypopituitarism | Pituitary Dwarfism | Chronic Granulomatous Disease, X-linked | Menetrier Disease | Acute Generalized Exanthematous Pustulosis | Joubert Syndrome 2 | Diabetic Encephalopathy | Sengers Syndrome | Infantile Nephropathic Cystinosis | Placenta Previa | Adenomyosis | Personality Disorders | Congenital Hypofibrinogenemia | Mevalonate Kinase Deficiency | Adenoma, Pituitary | Pseudoexfoliation Syndrome | Schindler Disease | Pleural Tuberculosis | Papillorenal Syndrome | Gyrate Atrophy Of The Choroid And Retina | Myotonic Disorders | Adenoma, Villous | Chronic Beryllium Disease | Intellectual Disability, Autosomal Dominant 5 | Blomstrand Osteochondrodysplasia | C3 Glomerulonephritis | Moyamoya Disease | Cluster Headache | Osteoporosis, Postmenopausal | Spondylosis | Alazami Syndrome | Ocular Albinism Type 1 | Spinal And Bulbar Muscular Atrophy | Waardenburg Syndrome Type 4 | Intracranial Hypertension | Schamberg Disease | Disseminated Superficial Actinic Porokeratosis | Anterior Segment Dysgenesis | Cervicitis | Hyperparathyroidism, Primary | Cirrhosis | Gastroenteritis, Eosinophilic | Renal Tubular Dysgenesis | Heterotopic Ossification | Episodic Ataxia | Sarcoidosis | Carotid Artery Disease | Anorectal Malformations | Acrodysostosis | Aspergillosis | Thalassemia | Anxiety Disorders | Fibrosis | Chitayat Syndrome | Hyperphenylalaninemia | Tardive Dyskinesia | B-cell Chronic Lymphocytic Leukemia | GNE Myopathy | X-linked Acrogigantism | Paraganglioma, Carotid Body | Microvillus Inclusion Disease | Schizophrenia, Paranoid | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Peters-plus Syndrome | Synovitis | Charcot-Marie-Tooth Disease, Type 1A | 3-hydroxy-3-methylglutaric Aciduria | Polymyositis | Pneumoconiosis | Limb Girdle Muscular Dystrophy | Hypotonia-cystinuria Syndrome | Panic Disorder | Superficial Spreading Melanoma | Diabetes Insipidus, Neurogenic | Haim-Munk Syndrome | Primary Biliary Cholangitis | Asphyxia Neonatorum | Silver-Russell Syndrome | Carbamoyl Phosphate Synthetase I Deficiency | Hyperbilirubinemia | Pyelonephritis | Anti-NMDA Receptor Encephalitis | Chronic Inflammatory Demyelinating Polyneuropathy | Spinocerebellar Ataxia Type 23 | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Paronychia | Sweet Syndrome | Coronary Artery Disease | Rhabdomyosarcoma | Arterial Tortuosity Syndrome | Lymphoproliferative Disorders | Beta-Propeller Protein-associated Neurodegeneration | Myofibromatosis | Exfoliative Dermatitis | Antley-Bixler Syndrome | Tyrosine Hydroxylase Deficiency | Autoimmune Polyendocrinopathy Syndrome Type I | Hyper IgE Syndrome | Delayed Sleep Phase Syndrome | HANAC Syndrome | Trichomegaly | Apert Syndrome | Episodic Ataxia Type 1 | Dentinogenesis Imperfecta | Dyskeratosis Congenita | Gastrointestinal Disorders | 3-methylglutaconic Aciduria Type IV | Situs Inversus | Gastroenteritis | Cancer, Prostate | Adenosine Deaminase Deficiency | Congenital Stromal Corneal Dystrophy | Polymyalgia Rheumatica | Charcot-Marie-Tooth Disease Type 2D | Metatropic Dysplasia | Isovaleric Acidemia | Fucosidosis | Hydrops Fetalis | DICER1 Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Infectious Diarrhea | Charcot-Marie-Tooth Disease Type 2E | Bronchiolitis | Amenorrhea | Small Lymphocytic Lymphoma | Hereditary Spastic Paraplegia | Panniculitis | Pyruvate Dehydrogenase Deficiency | DRESS Syndrome | Fabry's Disease | Epidermolytic Ichthyosis, Annular | Pigment Dispersion Syndrome | Common Cold | Mucolipidosis Type III | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Basal Ganglia Disease | Chronic Lymphocytic Leukemia | Hyperkalemic Periodic Paralysis | Behavioral Variant Of Frontotemporal Dementia | Craniofrontonasal Syndrome | Early Infantile Epileptic Encephalopathy 1 | Hypocalcemia | Epidermolysis Bullosa Simplex | Macrodactyly | Noonan Syndrome-like Disorder With Loose Anagen Hair | Charcot-Marie-Tooth Disease Type 3 | Spondylocostal Dysostosis | Osteomyelitis | Bietti Crystalline Dystrophy | Familial Hypobetalipoproteinemia | Brenner Tumor | Swine Influenza | Kashin-Beck Disease | Juvenile Polyposis | Multiple Sclerosis, Relapsing-remitting | Endophthalmitis | Beckwith-Wiedemann Syndrome | Phenylketonuria | Schwartz-Jampel-Aberfeld Syndrome | Spinocerebellar Ataxia Type 21 | Carcinoma, Small Cell | Cardiac Sarcoidosis | Leukocyte Adhesion Deficiency Type 1 | Congenital Absence Of Vas Deferens | Colitis, Lymphocytic | Hypokalemia | Nail Disorder, Nonsyndromic Congenital | Prurigo Nodularis | Sorsby Fundus Dystrophy | Schizotypal Personality Disorder | Hereditary Multiple Exostoses | Carcinoma, Signet Ring Cell