Lyme Disease

About the Disease
Lyme Disease, also known as lyme borreliosis, is related to babesiosis and mononeuritis multiplex, and has symptoms including fever, headache and fatigue. An important gene associated with Lyme Disease is YBX3 (Y-Box Binding Protein 3), and among its related pathways/superpathways are Innate Immune System and Disease. The drugs Phenoxymethylpenicillin and Amoxicillin have been mentioned in the context of this disorder. Affiliated tissues include heart, spinal cord and skin, and related phenotypes are arthritis and cranial nerve paralysis

Common Targets
G3620 | IL1RN

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Other Diseases

Sleep Apnea | Neuromyelitis Optica | Camptocormia | Chromosome 5q Deletion Syndrome | Cystitis | Alveolar Capillary Dysplasia | Early Infantile Epileptic Encephalopathy 1 | Cabezas Syndrome | Hypospadias | Congenital Disorders Of Glycosylation Type II | Constipation | Tetanus | Metatropic Dysplasia | Myopathy | Gastritis | Prostatitis | Kaposi Sarcoma | Chronic Myelomonocytic Leukemia | Acute Motor Axonal Neuropathy | Heterotaxy | Gardner Syndrome | Sarcoidosis, Pulmonary | Diabetes Type 2 | Polymyositis | Tuberculous Meningitis | Pulmonary Veno-occlusive Disease | Imerslund-Grasbeck Syndrome | Multiple Sclerosis | Diabetic Nephropathy | Rhizomelic Chondrodysplasia Punctata | Mitochondrial Myopathy | Multisystemic Smooth Muscle Dysfunction Syndrome | Jacobsen Syndrome | Cervicitis | Myotonic Disorders | Rhinitis | Chiari Malformation Type I | Subacute Sclerosing Panencephalitis | Rhabdomyosarcoma, Alveolar | Celiac Disease | Hyperthyroidism | Hyperferritinemia-cataract Syndrome | Guanidinoacetate Methyltransferase Deficiency | Angiosarcoma | Larsen Syndrome | Extramammary Paget's Disease | Cardiomyopathy, Restrictive | ADNP Syndrome | Arthritis | Pantothenate Kinase-associated Neurodegeneration | CDKL5 Deficiency Disorder | Common Variable Immunodeficiency | Spitz Nevus | Heart Block | Cerebrovascular Disorders | Antisynthetase Syndrome | Fukuyama Congenital Muscular Dystrophy | Cranial Nerve Disease | Gastric Atrophy | Hereditary Sensory And Autonomic Neuropathy | Angioedema, Acquired | Glaucoma | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Sweet Syndrome | Hypotonia-cystinuria Syndrome | Blau Syndrome | Cryptosporidiosis | Saethre-Chotzen Syndrome | Glycogen Storage Disease Type 9 | Axenfeld-Rieger Syndrome | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Microphthalmia | Episodic Ataxia Type 1 | Pontocerebellar Hypoplasia | Astrocytoma | Amenorrhea | Fragile X Syndrome | Congenital Heart Block | Progressive Myoclonic Epilepsy | MELAS Syndrome | Ischemia | Crigler-Najjar Syndrome | Liebenberg Syndrome | Desbuquois Syndrome | Hypotrichosis Simplex | Leukocyte Adhesion Deficiency Type 1 | Glaucomatocyclitic Crisis | Dengue Hemorrhagic Fever | Mitochondrial Disease | Asthma, Nocturnal | Non-proliferative Diabetic Retinopathy | Duchenne Muscular Dystrophy | Esophageal Adenocarcinoma | Pseudohypoparathyroidism Type 1B | Hypotrichosis | Ichthyosis | Superficial Spreading Melanoma | Hyperkeratosis | Photosensitivity | Autosomal Recessive Bestrophinopathy | Sick Sinus Syndrome 1 | Malignant Peripheral Nerve Sheath Tumor | Hepatitis D | Vascular Calcification | Rift Valley Fever | Facioscapulohumeral Muscular Dystrophy Type 1 | X-linked Sideroblastic Anemia | Antithrombin III Deficiency | Measles | Progressive Familial Intrahepatic Cholestasis Type 3 | Usher Syndrome Type I | Fetal And Neonatal Alloimmune Thrombocytopenia | Schistosomiasis Mansoni | Choroiditis | Alopecia Totalis | Dermatitis | Tyrosinemia | Tracheal Disorders | Burn-McKeown Syndrome | Erysipelas | Granuloma Annulare | Congenital Tufting Enteropathy | Noonan Syndrome | Achromatopsia | Adenosine Deaminase 2 Deficiency | Fibromyalgia | Multiple Sclerosis, Secondary Progressive | Incontinentia Pigmenti | Pulmonary Sclerosing Hemangioma | Neuromuscular Disorders | Spinocerebellar Ataxia | Netherton Syndrome | Cluster Headache | Ectrodactyly | Pituitary Disorders | Spina Bifida | Lattice Corneal Dystrophy Type 1 | Adenoma, Pleomorphic | Wolfram Syndrome 2 | Methemoglobinemia Type IV | Charcot-Marie-Tooth Disease | Transthyretin-related Amyloidosis | Fanconi Anemia | Low Tension Glaucoma | Giant Cell Arteritis | Tyrosinemia Type 1 | Intermittent Explosive Disorder | Mohr-Tranebjaerg Syndrome | Spondylometaphyseal Dysplasia | Pulmonary Alveolar Microlithiasis | Cardiospondylocarpofacial Syndrome | Menetrier Disease | Dyskeratosis Congenita | Hyperbilirubinemia, Neonatal | Spinocerebellar Ataxia Type 6 | Yellow Fever | Arteriosclerosis | Inborn Errors Of Metabolism | Marinesco-Sjogren Syndrome | Ellis-Van Creveld Syndrome | Pseudoexfoliation Syndrome | Blepharitis | Dysmorphophobia | Carcinoma, Merkel Cell | Acrocallosal Syndrome | Hypertension, Portal | Huntington's Disease | GAPO Syndrome | Mesothelioma, Malignant | Chronic Beryllium Disease | MIRAGE Syndrome | Acromesomelic Dysplasia | Facioscapulohumeral Muscular Dystrophy Type 2 | Spinocerebellar Ataxia Type 40 | Lipid Metabolism Disorders | Congenital Myopathy | Persistent Fetal Circulation | Parkinsonism | Scapuloperoneal Spinal Muscular Atrophy | Waardenburg Syndrome Type 4 | Sporadic Inclusion Body Myositis | Still Disease | Pituitary Stalk Interruption Syndrome | Sengers Syndrome | Japanese Encephalitis | Raine Syndrome | Agammaglobulinemia | Sporadic Hemiplegic Migraine | Hypervalinemia | Behcet's Disease | Chronic Periodontitis | Temtamy Preaxial Brachydactyly Syndrome | Cirrhosis | Vitamin A Deficiency | Focal Facial Dermal Dysplasia | Wiedemann-Steiner Syndrome | Hydrocephalus | Leukoencephalopathy, Progressive Multifocal | Stroke, Hemorrhagic | Lichen Planus | Retinoblastoma | Fontaine Progeroid Syndrome | Episodic Ataxia | Necrobiosis Lipoidica | Erdheim-Chester Disease | Retinal Dystrophy | CEDNIK Syndrome | Myocarditis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Anorchia | Polycystic Liver | Colitis, Lymphocytic | Hypoalbuminemia | Urticaria | Hyperinsulinemic Hypoglycemia | Papulopustular Rosacea | Colitis, Collagenous | Scleroderma, Diffuse | Nemaline Myopathy 8 | Pyloric Stenosis, Infantile Hypertrophic | Pierpont Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | ICF Syndrome | Lymphangioma | Epidermolytic Hyperkeratosis | Cancer, Skin | Ectodermal Dysplasia | Majeed Syndrome | Retinoschisis | Sarcosinemia | Leri-Weill Dyschondrosteosis | Oculocutaneous Albinism | Whipple's Disease | Arthritis, Reactive | Heimler Syndrome | Multifocal Motor Neuropathy | Ichthyosis Hystrix, Curth-Macklin Type | Primary Progressive Aphasia | Hypopituitarism | Nasodigitoacoustic Syndrome | Hemochromatosis Type 2 | Amyotrophic Lateral Sclerosis, Juvenile | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Anuria | Chronic Myeloid Leukemia | Chylomicron Retention Disease | Osteogenesis Imperfecta Type IV | Oculodentodigital Dysplasia | Nephropathy | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Patent Foramen Ovale | Scleroderma | Familial Hypobetalipoproteinemia | Pendred Syndrome | Leishmaniasis, Visceral | Bartsocas-Papas Syndrome | IgA Deficiency | Carotid Artery Disease | Encephalopathy, Hepatic | Venous Insufficiency | Hyperthermia, Malignant | Hereditary Coproporphyria | Desmosterolosis | Localized Scleroderma | Vasculitis | Analgesia | Exocrine Pancreatic Insufficiency | Sulfite Oxidase Deficiency | Prurigo Nodularis | Pterygium | Dysfibrinogenemia | Barrett Esophagus | Viral Meningitis | Nephrotic Syndrome | Familial Male-limited Precocious Puberty | Multiple Myeloma | Rubinstein-Taybi Syndrome | Craniometaphyseal Dysplasia | Perivascular Epithelioid Cell Tumor | Carcinoma, Small Cell | Arteriovenous Malformations | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Guillain-Barre Syndrome | Progressive Familial Intrahepatic Cholestasis Type 2 | Creatine Deficiency Syndrome Due To AGAT Deficiency | Polycystic Ovary Syndrome | HUPRA Syndrome | Polymyalgia Rheumatica | Glanzmann Thrombasthenia | Optic Nerve Hypoplasia, Bilateral | Pyelonephritis | POEMS Syndrome | Goiter, Nodular | Methemoglobinemia | Maternally Inherited Diabetes And Deafness | Nail-Patella Syndrome | Panniculitis | Paronychia | Conjunctivitis | Macular Degeneration | Sandhoff Disease | Botulism | Hypobetalipoproteinemias | Paternal Uniparental Disomy Of Chromosome 14 | Granular Corneal Dystrophy | Hyperparathyroidism | Carbohydrate Metabolism Disorders | Antisocial Personality Disorder | Congenital Ichthyosiform Erythroderma | IMAGe Syndrome | Hypoplastic Left Heart Syndrome | Alopecia Areata | Lyme Disease | Peritonitis | Tuberculosis | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Parvovirus B19 Infection | Blastomycosis | Idiopathic Pulmonary Fibrosis | Varices | Non-small Cell Lung Cancer | Hyperoxaluria | Nutrition Disorders | Multiple System Atrophy | Hereditary Neuropathy With Liability To Pressure Palsies | Adenylosuccinate Lyase Deficiency | Cantu Syndrome | Tylosis With Esophageal Cancer | Chronic Neutrophilic Leukemia | Distal Myopathy | Limb Girdle Muscular Dystrophy | Pre-eclampsia | DRESS Syndrome | Aplasia Cutis Congenita | Osteomyelitis | Pleural Tuberculosis | Asthma | Hemochromatosis Type 1 | Spinocerebellar Ataxia Type 2 | Leiomyosarcoma | Charcot-Marie-Tooth Disease Type 3 | Tendinitis | Tinea Versicolor | Neurofibrosarcoma | Hepatitis E | Autosomal Recessive Spastic Paraplegia Type 54 | Pouchitis | Xeroderma Pigmentosum Variant Type | Schamberg Disease | Brachydactyly | Sclerosteosis 2 | HANAC Syndrome | Alcoholism | Hypotension, Orthostatic | Urolithiasis | Gastrointestinal Disorders | Lymphoma, Mantle Cell | Mosaic Variegated Aneuploidy Syndrome 2 | Gynecomastia | Sjogren Syndrome | Papilloma | Focal Cortical Dysplasia Type 2 | Lymphoma, AIDS-related | Hypercalcemia | Sotos Syndrome | Intestinal Hypomagnesemia 1 | Melanoma, Uveal | Gray Platelet Syndrome | Speech Disorders | Hypertelorism | Creatine Deficiency Syndrome | Intestinal Tuberculosis | Vitamin B12 Deficiency | Craniofrontonasal Syndrome | Primary Torsion Dystonia | Clouston Hidrotic Ectodermal Dysplasia | GM2-gangliosidosis AB Variant | Motor Neuron Diseases | Niemann-Pick Disease, Type C | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Dominant Optic Atrophy | Proctitis | Fabry's Disease | Ehlers-Danlos Syndrome | Hemoglobinopathies | Wolff-Parkinson-White Syndrome | Pineoblastoma | Melanocytic Nevus | Amish Infantile Epilepsy Syndrome | Cutaneous Mastocytosis | B-cell Chronic Lymphocytic Leukemia | Molybdenum Cofactor Deficiency | Tibial Muscular Dystrophy | Parapsoriasis | Neurogenic Bladder | Coronary Restenosis | Esophagitis | GATA2 Deficiency | Renal Hypomagnesemia 3 | Juvenile Polyposis