Disease

Epidermodysplasia Verruciformis

About the Disease
Epidermodysplasia Verruciformis 1, also known as epidermodysplasia verruciformis, is related to pityriasis versicolor and skin carcinoma, and has symptoms including lesions on the body An important gene associated with Epidermodysplasia Verruciformis 1 is TMC6 (Transmembrane Channel Like 6), and among its related pathways/superpathways is "Aminoglycoside Ototoxicity Pathway, Adverse Drug Reaction". The drugs Glycolic acid and Ethanol have been mentioned in the context of this disorder. Affiliated tissues include skin, bone marrow and myeloid, and related phenotypes are seborrheic dermatitis and papule

Common Targets
LCK | KRT5 | ITK | RHOH | JAK1 | CD28 | TMC8

疾病靶点研报
Epidermodysplasia Verruciformis

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

Other Diseases

Neuroleptic Malignant Syndrome | Huntington's Disease | Sitosterolemia | Amelanotic Melanoma | Rhabdomyosarcoma, Alveolar | Ophthalmoplegia | Ornithine Transcarbamylase Deficiency | Thromboembolism | Osteoporosis-pseudoglioma Syndrome | Campomelic Dysplasia | Desbuquois Syndrome | Skin Papilloma | Congenital Ichthyosiform Erythroderma | Heart Septal Defects | ICF Syndrome | Familial Glucocorticoid Deficiency | Neurofibrosarcoma | Adenomyosis | Brachydactyly | Angiomyolipoma | Hemorrhoids | Meningeal Melanocytoma | NGLY1 Deficiency | Infertility | Intracranial Hypertension | Potocki-Shaffer Syndrome | Angina Pectoris | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Nemaline Myopathy | Polymyalgia Rheumatica | Hairy Cell Leukemia | Fucosidosis | Spondyloarthritis | H Syndrome | Crimean-Congo Hemorrhagic Fever | Poretti-Boltshauser Syndrome | Inflammatory Bowel Disease | Diabetes Type 2 | Dyggve-Melchior-Clausen Disease | Fibromyalgia | Leiomyosarcoma | Kindler Syndrome | L-2-Hydroxyglutaric Aciduria | Progressive Familial Intrahepatic Cholestasis Type 1 | Infertility, Male | Gastroenteritis, Eosinophilic | Ollier Disease | Cirrhosis | Arrhythmogenic Right Ventricular Cardiomyopathy | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Tuberculosis | Mosaic Variegated Aneuploidy Syndrome 2 | Robinow Syndrome | Pneumonia, Mycoplasma | Nail-Patella Syndrome | Neonatal Progeroid Syndrome | Hartsfield Syndrome | Cholestasis, Intrahepatic | Antisocial Personality Disorder | Malignant Fibrous Histiocytoma | Hereditary Pyropoikilocytosis | Distal Myopathy 2 | Nephritis, Interstitial | Neurocutaneous Syndromes | Renal Oncocytoma | Persistent Truncus Arteriosus | Charcot-Marie-Tooth Disease | Multicentric Carpotarsal Osteolysis Syndrome | Anosmia, Congenital | Pityriasis Rubra Pilaris | Tonsillitis | Waardenburg Syndrome Type 4A | Primary Erythromelalgia | Colon Adenoma | Diffuse Intrinsic Pontine Glioma | Congenital Afibrinogenemia | Diabetic Macular Edema | Rash | Charcot-Marie-Tooth Disease, Type 2 | Cat Eye Syndrome | Charcot-Marie-Tooth Disease, Type 2C | Hemorrhage | Fanconi Anemia | Spinocerebellar Ataxia Type 23 | Alkaptonuria | Progressive Familial Intrahepatic Cholestasis Type 3 | Leukemia | Spinocerebellar Ataxia | Familial Pheochromocytoma-paraganglioma | Pulverulent Zonular Cataract | Hyperparathyroidism, Secondary | Anencephaly | Prune Belly Syndrome | Posterior Polar Cataract | Cluster Headache | Obesity | Seminoma | Congenital Heart Defects | Interstitial Lung Diseases | Okihiro Syndrome | Pierson Syndrome | VACTERL/VATER Association | Chylomicron Retention Disease | Tendinopathy | Chondrodysplasia Punctata 2, X-linked Dominant | Tay-Sachs Disease | Carcinoid Tumor | Hypertensive Nephropathy | Roberts Syndrome | Nijmegen Breakage Syndrome | Osteogenesis Imperfecta | Tetraplegia | Primary Biliary Cholangitis | Neuroendocrine Cancer | Cherubism | Spinocerebellar Ataxia Type 2 | Craniosynostosis | Chanarin-Dorfman Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Epilepsy | Blood Protein Disorders | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Delirium | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Split Hand-foot Malformation | Cavitary Optic Disc Anomalies | Gout | Pemphigoid | Schistosomiasis | Low Tension Glaucoma | Anuria | POEMS Syndrome | Basal Ganglia Cerebrovascular Disease | Ameloblastoma | Seborrheic Dermatitis | Pain | Liver Failure | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Majeed Syndrome | Ventricular Septal Defect | Parapsoriasis | Carcinoma, Merkel Cell | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Aplasia Cutis Congenita | Muckle-Wells Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Hyperinsulinemic Hypoglycemia | LEOPARD Syndrome | Episodic Ataxia Type 1 | Non-proliferative Diabetic Retinopathy | Walker-Warburg Syndrome | Oculocutaneous Albinism Type 1 | Panic Disorder | Arthritis | Pituitary Disorders | Muscle Wasting | Waldenstrom Macroglobulinemia | Blepharospasm | Holoprosencephaly | Pituitary Stalk Interruption Syndrome | Vulvovaginitis | Ulcerative Colitis | Cardiofaciocutaneous Syndrome | Lymphangioleiomyomatosis | Autoimmune Disease | Brooke-Spiegler Syndrome | Esophageal Adenocarcinoma | Carcinoid Syndrome | Batten Disease | Succinic Semialdehyde Dehydrogenase Deficiency | Papillon-Lefevre Syndrome | Atopic Dermatitis | Niemann-Pick Disease, Type B | Niemann-Pick Disease, Type C | Hodgkin Lymphoma | Autoimmune Hemolytic Anemia | Hydrolethalus Syndrome | VACTERL Association | Exfoliative Dermatitis | Chronic Kidney Disease | Thrombophlebitis | Fibrillation, Atrial | Familial Retinal Arterial Macroaneurysm | Intestinal Hypomagnesemia 1 | Vitamin A Deficiency | Porphyria, Acute Intermittent | Hypodontia | Tatton-Brown-Rahman Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Gnathodiaphyseal Dysplasia | Polymyositis | Infantile Nephropathic Cystinosis | Charcot-Marie-Tooth Disease Type 4D | Spinocerebellar Ataxia Type 5 | Meckel-Gruber Syndrome | Epidermolytic Hyperkeratosis | Parkinson Disease 6, Autosomal Recessive Early-onset | Strabismus | Goiter | Encephalitis, Tick-borne | Centronuclear Myopathy | Salla Disease | Graft-versus-host Disease | Bernard-Soulier Syndrome | Neutropenia | Hepatitis | Spastic Paraplegia Type 7 | Hennekam Lymphangiectasia-lymphedema Syndrome | Pierpont Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Proteus Syndrome | Microphthalmia, Syndromic 7 | Hypohidrotic Ectodermal Dysplasia | Microcephalic Primordial Dwarfism | Panuveitis | Autism | Diabetes Mellitus, Transient Neonatal | Psoriasis | Beta-Propeller Protein-associated Neurodegeneration | Shwachman-Bodian-Diamond Syndrome | Pupil Disorders | Ileitis | 3-methylcrotonyl-CoA Carboxylase Deficiency | Glycogen Storage Disease Type 4 | Spinocerebellar Ataxia Type 7 | Shock, Cardiogenic | Osteogenesis Imperfecta Type V | Hypospadias | Hepatorenal Syndrome | Takotsubo Cardiomyopathy | Dysmorphophobia | Porphyria Cutanea Tarda | Adenosine Deaminase Deficiency | Charcot-Marie-Tooth Disease Type 3 | Mitochondrial Cytopathy | Meningitis | Familial Mediterranean Fever | Presbycusis | Gyrate Atrophy Of The Choroid And Retina | Autoimmune Polyendocrine Syndrome | Scleroderma, Diffuse | Turner's Syndrome | Lattice Corneal Dystrophy | Torticollis | Pyruvate Decarboxylase Deficiency | Oculocutaneous Albinism Type 2 | Esthesioneuroblastoma | Myhre Syndrome | Hereditary Mixed Polyposis Syndrome | Vascular Calcification | Emery-Dreifuss Muscular Dystrophy | Gitelman Syndrome | Lamellar Ichthyosis | Diabetic Nephropathy | Spinocerebellar Ataxia Type 31 | Myotonia | Chronic Inflammatory Demyelinating Polyneuropathy | Osteonecrosis Of The Jaw | Blepharo-cheilo-odontic Syndrome | Dystonia | Sensorineural Hearing Loss | Mitochondrial Disease | Osteoporosis, Postmenopausal | Ichthyosis Hystrix, Curth-Macklin Type | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Hypermetropia | Rubinstein-Taybi Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Intellectual Disability, Autosomal Dominant 5 | Corneal Ulcer | Beare-Stevenson Syndrome | Pleural Tuberculosis | Dupuytren Disease | Hypertension, Portal | Pleomorphic Xanthoastrocytoma | Dentinogenesis Imperfecta | Cardiomyopathy, Hypertrophic | Neuromuscular Disorders | Motor Neuron Diseases | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Babesiosis | Angioedema | Acute Generalized Exanthematous Pustulosis | Glutaric Aciduria Type 2 | Eosinophilia | Mumps | T-cell Chronic Lymphocytic Leukemia | Charcot-Marie-Tooth Disease Type 2D | Muscular Dystrophy | Vitreoretinal Degeneration, Snowflake Type | Sleep Apnea, Obstructive | Myofibrillar Myopathy | Microvillus Inclusion Disease | Systemic Lupus Erythematosus | Mountain Sickness | Niemann-Pick Disease, Type A | Irritable Bowel Syndrome | Ellis-Van Creveld Syndrome | Cardiac Arrest | Impulse Control Disorder | Ichthyosis, X-linked | Schizotypal Personality Disorder | Anodontia | Spinocerebellar Ataxia Type 13 | Infantile Refsum Disease | Cholecystitis | Menetrier Disease | Exotropia | Auriculocondylar Syndrome | Binge Eating Disorder | Chylothorax, Congenital | Autoimmune Autonomic Ganglionopathy | Scoliosis | Leri-Weill Dyschondrosteosis | Membranous Nephropathy | Fibrodysplasia Ossificans Progressiva | Narcolepsy | Acute Anterior Uveitis | X-linked Myotubular Myopathy | 5-oxoprolinase Deficiency | Asperger Syndrome | Epidermolysis Bullosa | Retinal Detachment | Craniopharyngioma | Birt-Hogg-Dube Syndrome | Saethre-Chotzen Syndrome | Immunoproliferative Disorders | Hemorrhagic Disorders | Hyperandrogenemia | Atrial Septal Defect | Corticobasal Syndrome | Vitreoretinopathy, Proliferative | Amelogenesis Imperfecta | Schizophrenia | Hypotension, Orthostatic | Autoimmune Polyendocrinopathy Syndrome Type I | Erythematotelangiectatic Rosacea | Keratoconus | Specific Granule Deficiency | Bicuspid Aortic Valve | Achondrogenesis | Perry Syndrome | Frank-ter Haar Syndrome | Carcinoma, Squamous Cell | Multisystemic Smooth Muscle Dysfunction Syndrome | Tardive Dyskinesia | Juvenile Polyposis | Bloom Syndrome | Methemoglobinemia Type IV | Myoclonus | Stuttering | Klippel-Feil Syndrome | Congenital Bilateral Absence Of Vas Deferens | Paget's Disease Of The Breast | Spinocerebellar Ataxia Type 27 | Familial Thoracic Aortic Aneurysm | Sleep Disorder | Pneumothorax | Long QT Syndrome Type 1 | Nephrosclerosis | Primary Ovarian Insufficiency | Coronary Heart Disease | Stargardt Disease | Whipple's Disease | Small Lymphocytic Lymphoma | Pyoderma Gangrenosum | Conduct Disorder | Ebstein Anomaly | Hypereosinophilic Syndrome | Mitochondrial Myopathy | Congenital Heart Block | Hereditary Xerocytosis | Paraganglioma, Carotid Body | Zygomycosis | Uveitis | Goiter, Nodular | Crouzon Syndrome With Acanthosis Nigricans | Celiac Disease | Nephronophthisis | Primary Sclerosing Cholangitis | Familial Dysautonomia | Astrocytoma | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Oculocutaneous Albinism Type 4 | Porphyria, Variegate | Cystinosis | Ocular Hypertension | Pneumonia, Bacterial | Pernicious Anemia | Peripheral Neuropathy | Anemia | VEXAS Syndrome | Combined Pituitary Hormone Deficiency | Pseudohypoparathyroidism Type 2 | Dubin-Johnson Syndrome | Osteitis | Ganglioglioma | Steel Syndrome | Spermatocele | Netherton Syndrome