Disease

Charcot-Marie-Tooth Disease

About the Disease
Charcot-Marie-Tooth Disease, also known as hereditary motor and sensory neuropathy, is related to charcot-marie-tooth disease, axonal, type 2e and charcot-marie-tooth disease and deafness, and has symptoms including back pain, headache and pain. An important gene associated with Charcot-Marie-Tooth Disease is MPZ (Myelin Protein Zero), and among its related pathways/superpathways are Neural crest differentiation and Intracellular trafficking proteins involved in CMT neuropathy. The drugs Folic acid and Lipoic acid have been mentioned in the context of this disorder. Affiliated tissues include Peripheral Nervous System, spinal cord and brain, and related phenotypes are no effect and no effect

Common Targets
YARS1 | LITAF | GARS1 | FDXR | SIGMAR1 | AARS1 | GDF11 | TRPV4 | MIR4635 | Gamma-Aminobutyric acid type B receptor | TRIM2 | SPG11 | PMP2 | ZDHHC17 | PDXK | RBM19 | PMP22 | FGD4 | NFATC1 | NRG1 | DYNC1H1 | ATP1A1 | ZFYVE27 | HSD17B4 | TRNV | DGAT2 | MORC2 | DCTN2 | HDAC7 | MPZ | SAMD9L | ADRA2A | Heat Shock Protein 27 (Hsp27) (nonspecified subtype) | IMPA1 | MIR3134 | COA7 | ROPN1L | HADHB | MCM3AP | PRX | DNM2 | GNB4 | EGR2 | FXN | NMDA receptor | TXNL4A | CSMD1 | MTRFR | SARS1 | MCPH1 | MME | TRPA1 | HARS1 | ATAD3A | CSRP2 | NDRG1 | IGHMBP2 | BSCL2 | ZWILCH | PPP1R12A | GABRA1 | DNMBP | LRSAM1 | SUCLA2 | SEPSECS | IARS1 | CLCN1 | LOC100507053 | VAC14 | HSPB8 | HINT1 | CCDC28B | PENK-AS1 | MFN2 | PYGM | G9734 | G1786 | PNKP | PLEKHG5 | MTMR2 | RPS20 | FAM210B | Class III phosphatidylinositol 3-kinase (PI3-kinase) sub-complex | C5orf34 | SACS | HK1 | CADM3 | MYH14 | FBXO38 | PIK3C3 | NKAIN3 | KIR2DL1 | SBF1 | DNAJB2 | DCTN1 | KARS1 | ARHGAP19 | SLC12A6 | FBLN5 | ANAPC1 | MSTN | SI | CCDC102B | MARS1 | NEFH | ARFGEF1 | SORD | AHNAK2 | FIG4 | HDAC6 | ARHGEF10 | NTRK2 | ADPRS | MFSD13A | GDAP1 | MYBL1 | HDAC2 | ACACA | MTPAP | BAG3 | SCO2 | NEFL | KIF1B | INF2 | ZNF236 | VEPH1 | SCN10A | LCTL | GPR17 | GJB1 | MARCHF6 | ADH1C | RAB7A | XKR4 | COX6A1 | CNTNAP1 | TRPV1 | NOTCH2NLC | MFN1 | SGPL1 | TFG | PDHB | AIFM1 | SH3TC2 | PPP1R15A

疾病靶点研报
Charcot-Marie-Tooth Disease

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

Other Diseases

Hypogammaglobulinemia | Opisthorchiasis | Echinococcosis | Multisystemic Smooth Muscle Dysfunction Syndrome | Central Retinal Artery Occlusion | Tinea Versicolor | Hernia, Inguinal | Budd-Chiari Syndrome | Diamond-Blackfan Anemia | Schizophrenia, Paranoid | Transthyretin-related Amyloidosis | Congenital Bilateral Absence Of Vas Deferens | Sarcoma, Alveolar Soft Part | Angioedema, Acquired | Barakat Syndrome | Smoldering Myeloma | Thrombocytopenia | Inborn Errors Of Metabolism | Congenital Sodium Diarrhea | Congenital Stationary Night Blindness | Mucolipidosis Type III | Osteogenesis Imperfecta Type II | Arthritis, Reactive | Niemann-Pick Disease, Type A | Iron Deficiency Anemia | Silicosis | Glycogen Storage Disease Type 3 | Osteogenesis Imperfecta Type III | Angelman Syndrome | Hereditary Spastic Paraplegia | Behcet's Disease | Pemphigoid | Retinitis Pigmentosa | Pericarditis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Pompe Disease | Fucosidosis | Autosomal Recessive Spastic Paraplegia Type 75 | Monilethrix | Potocki-Shaffer Syndrome | IgA Nephropathy | Trismus-pseudocamptodactyly Syndrome | Familial Hypobetalipoproteinemia | Hyperphenylalaninemia | Mannosidase Deficiency Diseases | Mucolipidosis Type II | Waardenburg Syndrome Type 4 | Infertility, Male | Apparent Mineralocorticoid Excess Syndrome | Lactose Intolerance | Discoid Lupus Erythematosus | Osteoporosis | Cat Eye Syndrome | Macrophage Activation Syndrome | Dermatitis Herpetiformis | Hemangioblastoma | Cyclic Vomiting Syndrome | Saethre-Chotzen Syndrome | Porphyria | Congenital Hypofibrinogenemia | Sleep Disorder | Measles | Sarcosinemia | Cardiac Arrest | Crimean-Congo Hemorrhagic Fever | Charcot-Marie-Tooth Disease Type 4E | Spinocerebellar Ataxia Type 3 | SAPHO Syndrome | Osteoarthritis | Dentinogenesis Imperfecta | Melanoma, Malignant | Toxic Epidermal Necrolysis | Hyperlipidemia Type V | Albinism | Congenital Stromal Corneal Dystrophy | Spinocerebellar Ataxia Type 13 | Angiosarcoma | Tyrosinemia Type 2 | Ameloblastic Carcinoma | Parvovirus B19 Infection | Esophageal Adenocarcinoma | Myotonia | Ileitis | Pneumonia, Mycoplasma | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Congenital Dyserythropoietic Anemia Type 1 | Stomatitis | Sickle Cell Anemia | Tetraplegia | Congenital Nephrotic Syndrome | Fundus Albipunctatus | Duane Retraction Syndrome | Intermittent Claudication | Methemoglobinemia Type IV | Urofacial Syndrome | Huntington's Disease | Lipid Storage Diseases | Skin Papilloma | Basal Ganglia Disease, Biotin-responsive | Cataract | Sponastrime Dysplasia | Diverticulitis | Juvenile Hyaline Fibromatosis | Alzheimer Disease, Late Onset | Melnick-Needles Syndrome | Hepatitis C, Chronic | Coloboma | Fukuyama Congenital Muscular Dystrophy | Iron Metabolism Disorders | Generalized Epilepsy And Paroxysmal Dyskinesia | Spinocerebellar Ataxia | Benign Familial Neonatal Convulsions | Glucagonoma | Restrictive Dermopathy | Malaria | Spermatocele | Urticaria | Leukemia-lymphoma, Adult T-cell | Plasma Cell Dyscrasia | Donnai-Barrow Syndrome | Irritable Bowel Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Chondrosarcoma | Congenital Hemolytic Anemia | Spondyloarthritis | Usher Syndrome | Schuurs-Hoeijmakers Syndrome | Enlarged Vestibular Aqueduct | Osteogenesis Imperfecta Type IV | Mitochondrial DNA Depletion Syndrome 13 | Blepharospasm | Pyruvate Dehydrogenase Deficiency | Giant Cell Glioblastoma | Unverricht-Lundborg Syndrome | Thrombosis | Greig Cephalopolysyndactyly Syndrome | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Hereditary Xerocytosis | Lipid Metabolism Disorders | Spinocerebellar Ataxia Type 23 | Relapsing Polychondritis | GLUT1 Deficiency Syndrome | Microcephaly, Seizures, And Developmental Delay | Malignant Fibrous Histiocytoma | Encephalocele | Schwartz-Jampel-Aberfeld Syndrome | Cerebellofaciodental Syndrome | Goiter, Nodular | Usher Syndrome Type I | Portal Vein Thrombosis | Sorsby Fundus Dystrophy | Okihiro Syndrome | Fahr Disease | Pulmonary Veno-occlusive Disease | Neurofibromatosis Type 1 | Coronary Restenosis | Polycystic Kidney, Autosomal Recessive | Oligoasthenoteratozoospermia | Larsen Syndrome | Chronic Mucocutaneous Candidiasis | Pyelonephritis | Vitreoretinopathy, Proliferative | Pure Red Cell Aplasia | Centronuclear Myopathy | Prurigo Nodularis | High Molecular Weight Kininogen Deficiency | Infantile Spasm | Saul-Wilson Syndrome | Niemann-Pick Disease, Type B | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Carcinoma, Squamous Cell | Pantothenate Kinase-associated Neurodegeneration | Christianson Syndrome | Retinopathy, Diabetic | Lipoma | Batten Disease | Incontinentia Pigmenti | Hemimegalencephaly | Adenosine Deaminase Deficiency | Lennox-Gastaut Syndrome | Bronchiectasis | Optic Neuropathy | Chronic Myelomonocytic Leukemia | Hypopigmentation | Hydrocephalus, Normal Pressure | Arthritis | Cartilage Disorders | Basan Syndrome | Cardiomyopathy, Dilated, 1L | Idiopathic Pulmonary Fibrosis | Waardenburg Syndrome | Granular Corneal Dystrophy | Huntington's Disease-like 2 | Charcot-Marie-Tooth Disease, Type 1A | Autoimmune Hemolytic Anemia | Renal Dysplasia | Myoclonic Atonic Epilepsy | Lymphoma, Follicular | Homocystinuria | Strabismus | Long QT Syndrome Type 2 | Non-epidermolytic Palmoplantar Keratoderma | Campomelic Dysplasia | Carcinoid Syndrome | Chloridorrhea, Congenital | Pathological Gambling | Paronychia | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Stuttering | HUPRA Syndrome | Coffin-Lowry Syndrome | Kearns-Sayre Syndrome | Tuberculosis | Disseminated Superficial Actinic Porokeratosis | Polycythemia | Congestive Heart Failure | Blepharitis | Spinocerebellar Ataxia Type 16 | Cancer, Kidney | Focal Facial Dermal Dysplasia | Corneal Neovascularization | Angiosarcoma Of The Breast | Acute Coronary Syndrome | Blepharophimosis Syndrome | Urea Cycle Disorder | Danon Disease | Glomerulonephritis, Membranous | Hypothyroidism | Limb Girdle Muscular Dystrophy | Pulmonary Alveolar Microlithiasis | Meningioma, Benign | Hypotrichosis Simplex | Erythrokeratodermia Variabilis | Meconium Ileus | Bronchitis | Sarcoidosis | Vitreoretinal Degeneration, Snowflake Type | Glycogen Storage Disease | Chorioretinitis | Megalencephaly | Cutaneous Lupus Erythematosus | Mitochondrial Disease | Glioblastoma | Cutaneous Mastocytosis | Major Depression | Alpha-thalassemia Myelodysplasia Syndrome | Pouchitis | Prolactinoma | Spinocerebellar Ataxia Type 8 | Thromboembolism | Vitamin B12 Deficiency | Diabetic Neuropathy | CREST Syndrome | Carney-Stratakis Syndrome | Depression | Hepatitis, Chronic | Fetal Akinesia Deformation Sequence | Retinal Coloboma | Glycogen Storage Disease Type 1b | Amyloidosis | Spinocerebellar Ataxia Type 7 | Fibrodysplasia Ossificans Progressiva | Haim-Munk Syndrome | Colitis, Collagenous | Proopiomelanocortin Deficiency | Pseudohypoaldosteronism | Pigment Dispersion Syndrome | Blepharoconjunctivitis | Constipation | Angiomyolipoma | Endometriosis | Osteoglophonic Dysplasia | Agoraphobia | Canavan Disease | Walker-Warburg Syndrome | Sezary Syndrome | Epidermodysplasia Verruciformis | Farber Disease | Subacute Sclerosing Panencephalitis | PHARC Syndrome | Nail-Patella Syndrome | Neuroblastoma | Common Variable Immunodeficiency | GATA2 Deficiency | Trichorhinophalangeal Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Aromatic L-amino Acid Decarboxylase Deficiency | Van Der Knaap Disease | Liver Failure, Acute Infantile | B-cell Chronic Lymphocytic Leukemia | Angina Pectoris | Anemia | Noonan Syndrome | Porphyria Cutanea Tarda | Insulin Resistance | Hereditary Coproporphyria | Exotropia | McLeod Syndrome | Lipodystrophy | Bicuspid Aortic Valve | Ellis-Van Creveld Syndrome | Congenital Mirror Movements | Learning Disability | Pseudohypoparathyroidism Type 1B | Frontometaphyseal Dysplasia | Imerslund-Grasbeck Syndrome | Congenital Diaphragmatic Hernia | Hypertension | Carbohydrate Metabolism Disorders | Congenital Heart Defects | Hereditary Hemorrhagic Telangiectasia | Focal Cortical Dysplasia Type 2 | Encephalitis | Atelosteogenesis Type 1 | Neovascular Glaucoma | Pearson Syndrome | Ovarian Hyperstimulation Syndrome | Stargardt Disease | Hereditary Sensory And Autonomic Neuropathy | Epiphyseal Chondrodysplasia, Miura Type | Smith-Kingsmore Syndrome | Poikiloderma With Neutropenia | WAGR Syndrome | Japanese Encephalitis | Pregnancy, Ectopic | Hemoglobinopathies | Cardiac Sarcoidosis | Glutaric Aciduria Type 3 | Charcot-Marie-Tooth Disease Type 4B1 | Mountain Sickness | Osteitis | Epithelial-myoepithelial Carcinoma | Axenfeld-Rieger Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Acne Vulgaris | Acquired Partial Lipodystrophy | Spondylolisthesis | Rift Valley Fever | Non-small Cell Lung Cancer | Hidradenitis Suppurativa | Cole-Carpenter Syndrome | Orthostatic Intolerance | Glycogen Storage Disease Type 4 | Kleine-Levin Syndrome | Ebstein Anomaly | Connective Tissue Disorders | Stickler Syndrome | Pulmonary Sclerosing Hemangioma | Sarcoidosis, Pulmonary | Ollier Disease | Epidermolysis Bullosa Simplex | HANAC Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Hypolipoproteinemia | Dominant Optic Atrophy | Antiphospholipid Syndrome | Trigonocephaly | Familial Exudative Vitreoretinopathy | Spinal Muscular Atrophy Type 2 | Myosin Storage Myopathy | Babesiosis | Motor Neuron Diseases | Polymyositis | Pfeiffer Syndrome | Leukocyte Adhesion Deficiency | Waardenburg Syndrome Type 2A | Enterocolitis, Necrotizing | Seizures-scoliosis-macrocephaly Syndrome | Glycogen Storage Disease Type 6 | Dyslexia | T-cell Leukemia | Progressive Familial Intrahepatic Cholestasis Type 3 | Creutzfeldt-Jakob Disease | Multiple Hamartoma Syndrome | Adenoid Cystic Carcinoma | Ganglioneuroma | Occipital Neuralgia | Chondrodysplasia Punctata 2, X-linked Dominant | Fetal Alcohol Syndrome | Rothmund-Thomson Syndrome | Auriculocondylar Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Anuria | Microcephaly | Spina Bifida | Papilloma | Craniofacial Dysostosis | Polymicrogyria | Gray Platelet Syndrome | Geleophysic Dysplasia | Spinal And Bulbar Muscular Atrophy | Jalili Syndrome | Recurrent Respiratory Papillomatosis | Hypertension, Renovascular | Birk-Barel Syndrome | Gangliosidosis | Hyper IgE Syndrome | Cutaneous Angiosarcoma | Fowler's Syndrome | Hairy Cell Leukemia