Disease

Neuropathy

About the Disease
Neuropathy, also known as peripheral neuropathy, is related to neuropathy, hereditary, with liability to pressure palsies and neuropathy, hereditary sensory and autonomic, type iia, and has symptoms including back pain, headache and neuralgia. An important gene associated with Neuropathy is DLX6-AS1 (DLX6 Antisense RNA 1), and among its related pathways/superpathways are Neural crest differentiation and EGR2 and SOX10-mediated initiation of Schwann cell myelination. The drugs Capsaicin and Mexiletine have been mentioned in the context of this disorder. Affiliated tissues include nerves, dorsal root ganglion and bone marrow, and related phenotypes are no effect and no effect

Common Targets
IL1B | G23411 | TARDBP | GARS1 | SLC28A3 | LOC100506071 | G3845 | FDXR | AARS1 | TRPV4 | SPTLC2 | ORAI1 | SFN | IL10 | FKBP4 | PMP22 | IL4R | MDK | SLC28A1 | RRM1 | WARS1 | NTRK1 | ABCC5 | HRH2 | Calcium release-activated channel (CRAC) | UBA5 | TSFM | GCK | Neurotrophic Factor (nonspecified subtype) | SLC22A12 | AKR1B1 | DDX39B | GSK3B | ABCC2 | SOD2 | NTRK3 | SLC6A4 | STOML3 | MPZ | SSTR3 | ERCC2 | ATP7A | Gap junction Connexin ( (nonspecified subtype) | CYP2C8 | IL-4 receptor | FAT3 | G4137 | PRX | NMDA receptor | SEPTIN9 | BICD2 | PDK3 | SLC19A1 | ANK1 | GSTP1 | RARB | GM1 ganglioside | KCNS1 | LOC100287329 | AGTR1 | SBF2 | CA7 | USP14 | TRPA1 | CYP3A5 | MME | POLG | IL1A | HARS1 | SCN11A | G472 | CCND3 | NDRG1 | IGHMBP2 | CA13 | SSTR4 | BSCL2 | SCN9A | TK2 | KIF5A | CHAF1A | LRSAM1 | GSTM1 | ROCK2 | HRH1 | mTOR complex 2 | SPIDR | NDUFAF6 | HSPB8 | KLC3 | HINT1 | WNK1 | MFN2 | APOE | IL4 | TYMS | CA2 | sigma Receptor (nonspecified subtype) | HMBS | ACTG2 | APEX1 | FPR2 | Potassium Channels (nonspecified subtype) | PARP2 | POLR1G | HSPB1 | EPOR | NMNAT2 | HK1 | OGA | SCN5A | SYT2 | AGTR2 | VCP | XRCC1 | SBF1 | DNAJB2 | SAMHD1 | SLC12A6 | DHFR | MARS1 | CDK6/Cyclin D3 | EPHA5 | HK2 | KRR1 | SLC5A7 | CYP11B2 | LOC105374608 | CYP4F2 | OPRM1 | G2475 | RIPK1 | Gap Junction Protein (nonspecified subtype) | VRK1 | HIF1A | IL18 | HDAC6 | CA14 | OTOF | G4780 | COCH | MTHFR | FIG4 | MYH7 | G5243 | NTRK2 | CA5B | ATL3 | FGD2 | CEP72-DT | GDAP1 | IL-13 receptor | KIF1A | Glutamate Receptor Ionotropic AMPA Receptor | AGXT | CYP3A4 | NEFL | ALDOB | CDK4 | NGF | SLCO1B3 | ADRA2C | IL12B | CEP72 | SLC31A1 | INF2 | SCN10A | Heat shock protein 90 (nonspecified subtype) | TUBB2A | TRPM3 | GJB1 | DCLRE1A | CDK4/Cyclin D3 | G142 | ERCC1 | G5743 | XPC | RRM2B | G7124 | SSTR2 | GJB2 | SLC6A2 | PRPS1 | MFN1 | C5 | EPHA6 | G9429 | HTR1A | Alpha-2 Adrenergic receptors (nonspecified subtype) | TTR | TFG | TUBB | CAPN10 | AIFM1 | FANCD2 | SH3TC2 | Kainate Receptor (GluR) (nonspecified subtype) | Voltage-Gated Sodium Channel Complex | KCNN3 | Sodium channel (nonspecified subtype) | MAP3K12 | LTA

疾病靶点研报
Neuropathy

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

Other Diseases

T-cell Prolymphocytic Leukemia | Myotonia | Hypertrophy | Hypertensive Retinopathy | Central Pain Syndrome | Silver-Russell Syndrome | Cancer, Colon | Goiter, Nodular | Nicolaides-Baraitser Syndrome | Growth Hormone Excess | Renal Hypomagnesemia 3 | Multiple Sulfatase Deficiency | Frontometaphyseal Dysplasia | Cancer, Skin | Tonsillitis | Kawasaki Disease | Lassa Fever | 3-methylcrotonyl-CoA Carboxylase Deficiency | Sarcoma, Alveolar Soft Part | Hartsfield Syndrome | Congenital Hereditary Endothelial Dystrophy Type I | Pierson Syndrome | REM Sleep Behavior Disorder | Arthritis | Tyrosinemia Type 2 | Parapsoriasis | Cryptosporidiosis | Keratoacanthoma | Cholestasis, Intrahepatic | Macrophagic Myofasciitis | Coma | Hermansky-Pudlak Syndrome | Intermittent Explosive Disorder | Fraser Syndrome | Steel Syndrome | Xeroderma Pigmentosum | Epidermodysplasia Verruciformis | Corneal Ulcer | Thrombocytopenia | Spinocerebellar Ataxia Type 14 | Lymphoproliferative Disease, X-linked | Carpal Tunnel Syndrome | Giant Axonal Neuropathy | Canavan Disease | Hereditary Spastic Paraplegia | Carcinoid Tumor | Papulopustular Rosacea | Insulin Resistance | Blau Syndrome | Corneal Dystrophies, Hereditary | Pneumonia, Mycoplasma | Anorectal Malformations | Hypertension, Portal | Clouston Hidrotic Ectodermal Dysplasia | Keratocystic Odontogenic Tumor | Anxiety Disorders | Nemaline Myopathy | Hypoalbuminemia | Stuve-Wiedemann Syndrome | Miyoshi Myopathy | Botulism | Lissencephaly 2 | VACTERL Association | Erectile Dysfunction | Glycogen Storage Disease Type 4 | Paraganglioma | Holoprosencephaly | Retinal Coloboma | Congenital Dyserythropoietic Anemia Type 4 | Smith-Magenis Syndrome | Retinal Degeneration | Congenital Mirror Movements | Thymoma, Malignant | Uveitis | Heart Failure | Fuchs Heterochromic Iridocyclitis | Anal Fissure | Rothmund-Thomson Syndrome | Blepharitis | Leishmaniasis, Visceral | Subcortical Band Heterotopia | Leukoplakia | Macular Corneal Dystrophy | Methemoglobinemia | Hyperlipidemia Type V | Rhabdomyosarcoma, Embryonal | Glanzmann Thrombasthenia | Hemangioendothelioma | Familial Partial Lipodystrophy | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Glioma | Polycystic Kidney, Autosomal Dominant | Bulimia Nervosa | Castleman Disease | Dementia, Vascular | Common Cold | Polyradiculopathy | Goldenhar Syndrome | Multiple Sclerosis, Chronic Progressive | Analgesia | Rhabdomyosarcoma, Alveolar | Enhanced S-cone Syndrome | Basal Ganglia Cerebrovascular Disease | Asthma | Kallmann Syndrome | Osteopathia Striata With Cranial Sclerosis | Congenital Tufting Enteropathy | Liver Failure, Acute Infantile | Spinocerebellar Ataxia Type 15 | Prune Belly Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Neurocutaneous Melanocytosis | Allergic Contact Dermatitis | Menetrier Disease | Atrial Septal Defect | Paronychia | Central Core Disease | Oculocutaneous Albinism | Scapuloperoneal Myopathy, X-linked Dominant | Eating Disorder | Congestive Heart Failure | Vitreoretinal Degeneration, Snowflake Type | Cutaneous T-cell Lymphoma | Angioedema, Acquired | Mosaic Variegated Aneuploidy Syndrome 2 | Pitt-Hopkins Syndrome | IgA Nephropathy | Colon Adenoma | Pseudoachondroplasia | Facioscapulohumeral Muscular Dystrophy | Nail Disorder, Nonsyndromic Congenital | Leukoencephalopathy, Progressive Multifocal | Crohn's Disease | Congenital Fiber-type Disproportion Myopathy | Krabbe Disease | Systemic Mastocytosis | Japanese Encephalitis | Smoldering Myeloma | Melanocytic Nevus | Keratosis | Kaposi Sarcoma | Knobloch Syndrome | Epidermolysis Bullosa Simplex, Localized | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Exocrine Pancreatic Insufficiency | Periventricular Nodular Heterotopia | Schwannomatosis | Gigantism | Carcinoma, Merkel Cell | Potocki-Shaffer Syndrome | Kabuki Syndrome 2 | Eiken Syndrome | Pseudohermaphroditism | Congenital Myopathy | Carbohydrate Metabolism Disorders | Chronic Mucocutaneous Candidiasis | Hypogammaglobulinemia | Posterior Polar Cataract | Autosomal Recessive Bestrophinopathy | Glioblastoma | Chanarin-Dorfman Syndrome | Exotropia | Temtamy Preaxial Brachydactyly Syndrome | Headache | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Gastroenteritis | Spinocerebellar Ataxia Type 17 | Wiedemann-Steiner Syndrome | Spinal Muscular Atrophy Type 2 | Mohr-Tranebjaerg Syndrome | Waardenburg Syndrome Type 1 | Rhabdoid Tumor | Granular Corneal Dystrophy Type 1 | Carey-Fineman-Ziter Syndrome | Nephrosclerosis | Meesmann Corneal Dystrophy | Brooke-Spiegler Syndrome | Walker-Warburg Syndrome | Coronary Heart Disease | Metachondromatosis | Polyarteritis Nodosa | Osteogenesis Imperfecta Type I | Abetalipoproteinemia | Cardiospondylocarpofacial Syndrome | Multicystic Renal Dysplasia | Craniometaphyseal Dysplasia | Multiple Hamartoma Syndrome | Cocaine-Related Disorders | Sclerosteosis | Woodhouse-Sakati Syndrome | Progressive Familial Intrahepatic Cholestasis Type 1 | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Cranioectodermal Dysplasia | Creatine Deficiency Syndrome | Keloid | Anovulation | Cholesteryl Ester Storage Disease | Communication Disorders | Chondrosarcoma | Sarcoma, Endometrial Stromal | Diabetes Insipidus, Nephrogenic | Juvenile Xanthogranuloma | Epidermolysis Bullosa Acquisita | Coffin-Siris Syndrome | Erysipelas | Glycogen Storage Disease Type 1b | POEMS Syndrome | SAPHO Syndrome | Chromosome 5q Deletion Syndrome | Glutaric Aciduria Type 1 | Osteogenesis Imperfecta Type V | Peters-plus Syndrome | Hepatic Steatosis | Sturge-Weber Syndrome | Tyrosinemia | Netherton Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Renal Medullary Carcinoma | Hyperostosis | Hypercalcemia | Oculodentodigital Dysplasia | Urolithiasis | Low Phospholipid Associated Cholelithiasis | Schwannoma | Acrodysostosis | Charcot-Marie-Tooth Disease Axonal Type 2N | Connective Tissue Disorders | Alazami Syndrome | Malaria | Glomerulonephritis, Membranoproliferative | Angelman Syndrome | Von Hippel-Lindau Disease | Retinoschisis | Endocarditis | Veno-occlusive Disease | Protein C Deficiency | Distal Myopathy 2 | Arts Syndrome | Celiac Disease | Large Granular Lymphocytic Leukemia | Syncope | Encephalocele | Tumoral Calcinosis | Pulverulent Zonular Cataract | Fukuyama Congenital Muscular Dystrophy | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Huntington's Disease-like 2 | Encephalopathy, Hepatic | Idiopathic Multicentric Castleman Disease | Hydrolethalus Syndrome | Joubert Syndrome 2 | Transcobalamin Deficiency | Neuroendocrine Cancer | Spasticity | Tremor | Myeloid Leukemia | Spinal Cord Diseases | Microcephalic Primordial Dwarfism | Lipoma | Myocarditis | Gastritis, Atrophic | Oculopharyngeal Muscular Dystrophy | Hypermethioninemia | PASLI Disease | Crigler-Najjar Syndrome | Blastomycosis | Donnai-Barrow Syndrome | Lipid Storage Myopathy | Presbycusis | Osmotic Demyelination Syndrome | Asplenia | Hemophilia | Hypersensitivity Pneumonitis | Charcot-Marie-Tooth Disease, Type 6 | Desmosterolosis | Kashin-Beck Disease | Persistent Mullerian Duct Syndrome | Batten Disease | Hyperparathyroidism, Primary | Multiple Epiphyseal Dysplasia | Lymphangiomatosis | Myelitis | Cutaneous Angiosarcoma | Acute Anterior Uveitis | Christianson Syndrome | Pituitary Stalk Interruption Syndrome | Varicocele | Hypotrichosis | Histoplasmosis | Fascioliasis | Chronic Idiopathic Myelofibrosis | Familial Digital Arthropathy-brachydactyly | Esophageal Carcinoma | Blue Nevus | Myopathy | Lichen Sclerosus | Hereditary Sensory Neuropathy Type 1 | Cardiac Arrest | Leukemia | Brachydactyly | Lymphedema-distichiasis Syndrome | Familial Pheochromocytoma-paraganglioma | Sertoli Cell-only Syndrome | Retinopathy Of Prematurity | Common Variable Immunodeficiency | Birt-Hogg-Dube Syndrome | Immunoproliferative Disorders | Amyloidosis | Congenital Poikiloderma | Lupus Erythematosus | Autonomic Neuropathy | Aplasia Cutis Congenita | Guanidinoacetate Methyltransferase Deficiency | Schistosomiasis Mansoni | Seminoma | Oculocutaneous Albinism Type 2 | Adenocarcinoma | Epidermolysis Bullosa | Diffuse Mesangial Sclerosis | Gout | Myopia | Ichthyosis, X-linked | Diabetic Encephalopathy | Pigment Dispersion Syndrome | Glycogen Storage Disease | Evans Syndrome | H Syndrome | Juvenile Myoclonic Epilepsy | Schnyder Crystalline Corneal Dystrophy | Hereditary Neuropathy With Liability To Pressure Palsies | Anthrax | Skin Carcinoma | Waardenburg Syndrome | Bone Giant Cell Tumor | Malignant Fibrous Histiocytoma | Mucolipidosis Type IV | Microcephaly | Extramammary Paget's Disease | Optic Atrophy 2 | Adrenoleukodystrophy, X-linked | NDH Syndrome | Blepharo-cheilo-odontic Syndrome | Pseudohypoaldosteronism | Eosinophilia | Exfoliative Dermatitis | Sensory Neuropathy | Vitamin B12 Deficiency | Acute Motor Axonal Neuropathy | Cryptococcal Meningitis | GM2-gangliosidosis AB Variant | Craniofrontonasal Syndrome | Nestor-Guillermo Progeria Syndrome | Congenital Dysfibrinogenemia | Cataplexy | Scapuloperoneal Spinal Muscular Atrophy | Myosin Storage Myopathy | Anorexia Nervosa | Facioscapulohumeral Muscular Dystrophy Type 2 | 5-oxoprolinase Deficiency | Pulmonary Sclerosing Hemangioma | Vasculitis | Leri-Weill Dyschondrosteosis | Gnathodiaphyseal Dysplasia | Lymphoma | Osteogenesis Imperfecta | Orthostatic Intolerance | Neurocysticercosis | Chronic Thromboembolic Pulmonary Hypertension | Aicardi-Goutieres Syndrome | Dystrophy, Cone-rod | Molybdenum Cofactor Deficiency | Hypoparathyroidism | Monilethrix | Reye Syndrome | Sengers Syndrome | Fetal Alcohol Syndrome | Lymphomatoid Granulomatosis | Tangier Disease | Iron Deficiency Anemia | KBG Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Meniere's Disease | Ulcerative Colitis | Hypothyroidism | Hyperferritinemia-cataract Syndrome | Trimethylaminuria | Spinocerebellar Ataxia Type 23 | Pyruvate Kinase Deficiency | Pearson Syndrome | Pleurisy | Dysmorphophobia | AIDS | Homocystinuria | Twin-to-twin Transfusion Syndrome | Peripheral T-cell Lymphoma | Stromal Corneal Dystrophy | Galactosemia | Postpoliomyelitis Syndrome | Aceruloplasminemia | Crisponi Syndrome