Acute Motor Axonal Neuropathy

About the Disease
Acute Motor Axonal Neuropathy, also known as acute pure motor guillain-barre syndrome, is related to guillain-barre syndrome and axonal neuropathy. The drugs Gabapentin and Amantadine have been mentioned in the context of this disorder. Affiliated tissues include brain, spinal cord and bone marrow.

Common Targets
GAN | TRPV4 | CD1A | CD1E | G7124

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

Other Diseases

Pelvic Inflammatory Disease | Atelosteogenesis Type 2 | Inflammatory Myopathy | Hereditary Sensory And Autonomic Neuropathy | Hepatitis, Alcoholic | Acanthosis Nigricans | CDKL5 Deficiency Disorder | Myopathy | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Diabetes Insipidus | Xeroderma Pigmentosum | Papilledema | Rickets | Prolidase Deficiency | Language Disorders | Cardiac Arrest | MIRAGE Syndrome | Acrocallosal Syndrome | Hermansky-Pudlak Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Coma | Amish Infantile Epilepsy Syndrome | Blomstrand Osteochondrodysplasia | Microcephalic Primordial Dwarfism | Glycogen Storage Disease Type 1b | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Acute Leukemia | Hyperphenylalaninemia | Corneal Edema | Cancer, Kidney | Stroke | Brachial Plexus Neuropathy | Duane Retraction Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Inflammatory Linear Verrucous Epidermal Nevus | Sporadic Inclusion Body Myositis | Urea Cycle Disorder | Anorchia | Congenital Hemolytic Anemia | Alstrom Syndrome | Infantile Nephropathic Cystinosis | Still Disease | Acrodysostosis | Adult Polyglucosan Body Disease | Mastitis | Rheumatic Heart Disease | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Cerebrotendinous Xanthomatosis | Autoimmune Polyendocrinopathy Syndrome Type I | Primary Hyperoxaluria | Primary Ovarian Insufficiency | Usher Syndrome Type II | Chronic Periodontitis | Anterior Segment Dysgenesis | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Pulmonary Veno-occlusive Disease | Adenocarcinoma | Presbycusis | Citrullinemia | Becker Muscular Dystrophy | Melanoma, Malignant | Autosomal Recessive Spastic Paraplegia Type 35 | Crisponi Syndrome | Takotsubo Cardiomyopathy | Postaxial Polydactyly | Glutaric Aciduria Type 2 | Coffin-Siris Syndrome | Alpha-1 Antitrypsin Deficiency | Common Cold | Borjeson-Forssman-Lehmann Syndrome | Pearson Syndrome | Peters-plus Syndrome | Pineoblastoma | Necrotizing Autoimmune Myopathy | Pfeiffer Syndrome | Fibronectin Glomerulopathy | Osteogenesis Imperfecta Type I | Lymphangiomatosis | Chronic Beryllium Disease | Myelomeningocele | Retinoschisis | Thromboembolism | Alpha-mannosidosis | Polymicrogyria | Pyruvate Kinase Deficiency | Gerstmann-Straussler-Scheinker Syndrome | Neurocysticercosis | Wolfram Syndrome 2 | Pheochromocytoma | Retinal Vasculitis | Gastritis | Neurodevelopmental Disorders | Hydrocephalus, Normal Pressure | HUPRA Syndrome | Rhizomelic Chondrodysplasia Punctata | Peutz-Jeghers Syndrome | Hypersensitivity Pneumonitis | Thalassemia, Beta | Exotropia | Neurodegeneration With Brain Iron Accumulation | Pupil Disorders | Ureteropelvic Junction Obstruction | Hyperglycemia | Myositis, Focal | Cystitis | Oculocutaneous Albinism Type 2 | Antley-Bixler Syndrome | GLUT1 Deficiency Syndrome | Rhabdomyosarcoma, Alveolar | Autosomal Recessive Bestrophinopathy | Craniofrontonasal Syndrome | Schwannoma | Portal Vein Thrombosis | Osteonecrosis Of The Jaw | Delayed Sleep Phase Syndrome | Pseudoachondroplasia | Barakat Syndrome | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Leber Hereditary Optic Neuropathy | PASLI Disease | Rhabdomyosarcoma, Embryonal | Hennekam Lymphangiectasia-lymphedema Syndrome | Neuroendocrine Cancer | Progressive Myoclonic Epilepsy | Rhabdoid Tumor | Cryptorchidism | Cockayne Syndrome | Behavioral Variant Of Frontotemporal Dementia | Osteopetrosis | Familial Hypertrophic Cardiomyopathy | Emery-Dreifuss Muscular Dystrophy | Thyroiditis | Colitis | Encephalitis | Poretti-Boltshauser Syndrome | Compartment Syndrome | Papulopustular Rosacea | Aneurysm, Abdominal Aortic | Congenital Nephrotic Syndrome | Hemolytic Anemia | Carbonic Anhydrase VA Deficiency | Osteomyelitis | Acute Tubular Necrosis | Spastic Paraplegia Type 7 | Cerebral Cavernous Malformations | Cervicitis | Central Core Disease | Systemic Lupus Erythematosus | Chondroma | Non-small Cell Lung Cancer | Membranous Nephropathy | Uterine Leiomyoma | Fibromyalgia | Autosomal Recessive Congenital Ichthyosis | Crouzon Syndrome With Acanthosis Nigricans | Progressive Familial Intrahepatic Cholestasis Type 3 | Palmoplantar Keratoderma | Disseminated Intravascular Coagulation | Stevens-Johnson Syndrome | Neutropenia | Familial Thoracic Aortic Aneurysm | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Arthritis, Reactive | Antithrombin III Deficiency | Adenoma, Pituitary | Pulmonary Vein Stenosis | Dysmorphophobia | Osteoglophonic Dysplasia | Anorexia Nervosa | Gestational Trophoblastic Disease | Pulmonary Tuberculosis | Optic Nerve Diseases | Anovulation | Angioedema, Acquired | Carotid Artery Disease | Biotinidase Deficiency | Spermatocele | Lipid Storage Diseases | Persistent Fetal Circulation | Hypokalemic Periodic Paralysis | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Allan-Herndon-Dudley Syndrome | Fuchs Dystrophy | Walker-Warburg Syndrome | Primary Cutaneous Amyloidosis | Personality Disorders | Hypertension, Essential | Goldenhar Syndrome | Autonomic Nervous System Disorders | Carcinoid Tumor | Raine Syndrome | Hepatitis E | Nemaline Myopathy 8 | Farber Disease | Tinea Versicolor | Fetal And Neonatal Alloimmune Thrombocytopenia | Epidermolysis Bullosa Dystrophica | Hemolytic Uremic Syndrome, Atypical | Nance-Horan Syndrome | Distal Myopathy | Cancer, Skin | Sarcoma, Alveolar Soft Part | Nail Disorder, Nonsyndromic Congenital | Vogt-Koyanagi-Harada Syndrome | Encephalitis, Tick-borne | Celiac Disease | Histiocytosis | Smith-Kingsmore Syndrome | Dowling-Degos Disease | Achondrogenesis | Addison Disease | Cardiofaciocutaneous Syndrome | Sepiapterin Reductase Deficiency | Thrombosis | Jacobsen Syndrome | GATA2 Deficiency | Sarcoma, Ewing | Nestor-Guillermo Progeria Syndrome | Nephritis, Interstitial | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Chromosome 16p11.2 Deletion Syndrome | Mast Cell Leukemia | Spinocerebellar Ataxia | Oculocutaneous Albinism | Chronic Granulomatous Disease, X-linked | Glycogen Storage Disease Type 6 | Erdheim-Chester Disease | Fibromuscular Dysplasia | Learning Disability | CEDNIK Syndrome | Desbuquois Syndrome | Dwarfism | Placenta Previa | Pseudohypoparathyroidism Type 1B | Coloboma | Hypertension, Portal | Platelet Disorders | Xeroderma Pigmentosum Variant Type | Iron Overload | Microtia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Headache | Sick Sinus Syndrome | Glomerulonephritis, Membranous | Inflammatory Bowel Disease | Glutaric Aciduria Type 1 | WAGR Syndrome | Sitosterolemia | Restless Legs Syndrome | Christianson Syndrome | Thrombocythemia, Essential | Epidermolytic Hyperkeratosis | Thanatophoric Dysplasia Type 1 | Hypoglycemia | HANAC Syndrome | Prolactinoma | Osteogenesis Imperfecta Type II | Trichotillomania | Leukoencephalopathy, Progressive Multifocal | Sensory Neuropathy | Esophageal Motility Disorders | Seizures | Familial Digital Arthropathy-brachydactyly | Common Variable Immunodeficiency | Beckwith-Wiedemann Syndrome | Connective Tissue Disorders | Pneumonia, Viral | Benign Familial Infantile Seizures | Amenorrhea | Pouchitis | Hypertension, Pulmonary | Polydactyly | Nager Acrofacial Dysostosis | Early Infantile Epileptic Encephalopathy 13 | McKusick Type Metaphyseal Chondrodysplasia | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Homocystinuria | Chitayat Syndrome | Asthma | Cyst | Seizures-scoliosis-macrocephaly Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Iron Deficiency Anemia | Lymphoproliferative Disorders | Premature Ejaculation | Pre-eclampsia | Corneal Dystrophy And Perceptive Deafness | Graves Disease | Diabetes Type 1 | Dupuytren Disease | Lathosterolosis | Microcephaly, Seizures, And Developmental Delay | Hyperoxaluria | Anti-NMDA Receptor Encephalitis | Urolithiasis | Gingivitis | Oguchi Disease-2 | Amyotrophic Lateral Sclerosis | Melanoma, Uveal | Herpes Simplex Dermatitis | Prader-Willi Syndrome | Multisystemic Smooth Muscle Dysfunction Syndrome | Porphyria, Acute Intermittent | Gnathodiaphyseal Dysplasia | Steel Syndrome | Glioma | Communication Disorders | Adrenoleukodystrophy, X-linked | Orthostatic Intolerance | Lymphoma, Follicular | Hereditary Xerocytosis | Osteitis | Majeed Syndrome | Hemochromatosis Type 2 | Reye Syndrome | Fibrosarcoma | Chromosome 9q34.3 Deletion Syndrome | Larsen Syndrome | Trichuriasis | Trachoma | Batten Disease | Chronic Kidney Disease | Ebstein Anomaly | Orotic Aciduria | Prolymphocytic Leukemia | Macrodactyly | Vestibular Disease | Cannabis Abuse | Neurocutaneous Syndromes | Epilepsy | Aplasia Cutis Congenita | Narcolepsy | Sarcoidosis, Pulmonary | Spondyloarthritis | Congestive Heart Failure | Thyroiditis, Autoimmune | Cardiomyopathy, Restrictive | Autism Spectrum Disorders | Clouston Hidrotic Ectodermal Dysplasia | Tumoral Calcinosis | Leiomyoma | Retinopathy, Diabetic | Nasodigitoacoustic Syndrome | Hemangioendothelioma | Parvovirus B19 Infection | Seasonal Mood Disorder | Arteriovenous Malformations | Progressive Familial Intrahepatic Cholestasis Type 2 | Diarrhea | Osteopathia Striata With Cranial Sclerosis | Gangliosidosis | T-cell Prolymphocytic Leukemia | Overactive Bladder | Menetrier Disease | Persistent Hyperplastic Primary Vitreous | Thrombophilia | Branchiootorenal Syndrome | Dengue Shock Syndrome | Senior-Loken Syndrome | Niemann-Pick Disease, Type A | Spitz Nevus | Molybdenum Cofactor Deficiency | Hemochromatosis | Optic Neuropathy | Renal Failure | Apparent Mineralocorticoid Excess Syndrome | Neurofibroma, Plexiform | Galloway-Mowat Syndrome | Irritable Bowel Syndrome | Vaginitis | Cerebellar Ataxia, Cayman Type | Adrenal Insufficiency | Scleritis | Intracranial Hypertension | Von Willebrand Disease | Chronic Enteropathy Associated With SLCO2A1 Gene | Rothmund-Thomson Syndrome | Aneurysm, Thoracic Aortic | Chromosome 5q Deletion Syndrome | Holoprosencephaly | Spondyloepiphyseal Dysplasia Tarda, X-linked | Oligoasthenoteratozoospermia | Hereditary Pyropoikilocytosis | Ganglioglioma | Neural Tube Defect | Tendinitis | Episodic Ataxia | Spinocerebellar Ataxia Type 8 | DOCK8 Immunodeficiency Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Lymphoma, Mantle Cell | Colorectal Adenoma | Malaria, Cerebral | Congenital Lipoid Adrenal Hyperplasia | Lymphangioleiomyomatosis | Cherubism | Hereditary Spherocytosis | Renal Oncocytoma | Cirrhosis | Chondrodysplasia Punctata 1, X-linked Recessive