Spinal Cord Diseases

About the Disease
Spinal Cord Disease, also known as spinal cord diseases, is related to vascular myelopathy and myelitis, and has symptoms including back pain, headache and hemiplegia. An important gene associated with Spinal Cord Disease is GDNF (Glial Cell Derived Neurotrophic Factor), and among its related pathways/superpathways are Neural Stem Cells and Lineage-specific Markers and Spinal cord injury. The drugs Sevoflurane and Pregabalin have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, bone marrow and bone, and related phenotypes are immune system and hematopoietic system

Common Targets
Metabotropic glutamate (mGluR) receptor (nonspecified subtype) | VDR | RAF1 | Cannabinoid receptor (nonspecified subtype) | SOS1

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

Other Diseases

Neutropenia | Duchenne Muscular Dystrophy | Pyelonephritis | Oligospermia | Autosomal Recessive Spastic Paraplegia Type 75 | Dowling-Degos Disease | Chediak-Higashi Syndrome | Absence Epilepsy | Glomerulonephritis | Hereditary Inclusion Body Myopathy | T-cell Leukemia | Ileitis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Vitamin A Deficiency | Creatine Deficiency Syndrome Due To AGAT Deficiency | Pierre Robin Syndrome | Hypoalbuminemia | Ganglioglioma | Joubert Syndrome | Autoimmune Disease | Spinocerebellar Ataxia Type 5 | Lymphoma, Mantle Cell | Neuromyelitis Optica | Torticollis | Sporadic Inclusion Body Myositis | Anal Fissure | Intestinal Tuberculosis | Nephritis, Interstitial | Histoplasmosis | Myosin Storage Myopathy | Low Phospholipid Associated Cholelithiasis | Blomstrand Osteochondrodysplasia | Intermittent Claudication | Heart Failure | Budd-Chiari Syndrome | Adenoma, Villous | Cysticercosis | Anorchia | Hypereosinophilic Syndrome | Guillain-Barre Syndrome | Congenital Ichthyosiform Erythroderma | Conjunctivitis, Allergic | Cholestasis | Essential Fructosuria | Seminoma | Okihiro Syndrome | LEOPARD Syndrome | Autism | Farber Disease | Eclampsia | Centronuclear Myopathy | Giant Cell Arteritis | Glycogen Storage Disease Type 1a | Anti-glomerular Basement Membrane Disease | Charcot-Marie-Tooth Disease, Type 6 | Dystonia-parkinsonism, X-linked | Marinesco-Sjogren Syndrome | Hydrops Fetalis | Congenital Afibrinogenemia | Silver-Russell Syndrome | Saethre-Chotzen Syndrome | Pyloric Stenosis, Infantile Hypertrophic | Leber Hereditary Optic Neuropathy | Dysmorphophobia | Antiphospholipid Syndrome | Chondrodysplasia Punctata 2, X-linked Dominant | Pituitary Disorders | NGLY1 Deficiency | Antley-Bixler Syndrome | Spinocerebellar Ataxia Type 13 | 3-hydroxy-3-methylglutaric Aciduria | Thyrotoxic Periodic Paralysis | Hepatorenal Syndrome | Progressive Familial Intrahepatic Cholestasis Type 1 | Common Cold | 3-methylglutaconic Aciduria | Retinal Vasculitis | Spinocerebellar Ataxia Type 40 | Herpes Simplex Dermatitis | H Syndrome | Robinow Syndrome | Fraser Syndrome | Carcinoma, Squamous Cell | Discoid Lupus Erythematosus | Necrotizing Autoimmune Myopathy | Urolithiasis | Epidermolysis Bullosa Acquisita | Megalencephaly | Juvenile Myelomonocytic Leukemia | Lymphangioma | Hypopigmentation | Pyruvate Decarboxylase Deficiency | Amelogenesis Imperfecta | Porphyria | Gastroenteritis | Pure Autonomic Failure | Acute Generalized Exanthematous Pustulosis | Bronchiolitis | Barakat Syndrome | Genee-Wiedemann Syndrome | Waardenburg Syndrome Type 2E | Leri Pleonosteosis | Arterial Tortuosity Syndrome | Osteogenesis Imperfecta Type VI | Neonatal Progeroid Syndrome | Intestinal Obstruction | Kohlschutter-Tonz Syndrome | Chromosome 8q21.11 Deletion Syndrome | Split Hand-foot Malformation | Acquired Partial Lipodystrophy | Congenital Aniridia | Retinal Detachment | Endometrial Hyperplasia | Eating Disorder | Lennox-Gastaut Syndrome | Hypercalciuria | Dermatomyositis | Intestinal Pseudo-obstruction | AIDS Dementia Complex | Tendinopathy | Pseudoachondroplasia | 5-oxoprolinase Deficiency | Pathological Gambling | Paraganglioma, Carotid Body | Takayasu's Arteritis | Multisystemic Smooth Muscle Dysfunction Syndrome | Lipodystrophy | Hypocalcemia | Chromosome 16p11.2 Deletion Syndrome | Cramp Fasciculation Syndrome | Hydrocephalus | Scoliosis | C3 Glomerulonephritis | Diabetes Type 1 | Rhinitis | Sandhoff Disease | Generalized Epilepsy With Febrile Seizures Plus | Urticaria | Nemaline Myopathy | Long QT Syndrome Type 2 | PASLI Disease | Constipation | Aicardi-Goutieres Syndrome | Graft-versus-host Disease | Chronic Myelomonocytic Leukemia | Myositis, Focal | Hepatopulmonary Syndrome | Fetal Akinesia Deformation Sequence | Cholecystitis | Pulmonary Veno-occlusive Disease | Proximal Symphalangism | Paternal Uniparental Disomy Of Chromosome 14 | Carcinoid Tumor | Vitamin B12 Deficiency | X-linked Myotubular Myopathy | Charcot-Marie-Tooth Disease Type 2T | Jalili Syndrome | Synovitis | Dermatitis | Muscle Wasting | Frontotemporal Dementia | Superficial Spreading Melanoma | Osteomyelitis | Fucosidosis | Greenberg Dysplasia | Scleroderma, Diffuse | Short-chain Acyl-CoA Dehydrogenase Deficiency | Spondylocostal Dysostosis | Thrombophlebitis | Hyperinsulinism-hyperammonemia Syndrome | Spermatocele | Adult Polyglucosan Body Disease | Hereditary Spastic Paraplegia | Spasticity | Neurodermatitis | Unverricht-Lundborg Syndrome | Muckle-Wells Syndrome | Vitreoretinal Degeneration, Snowflake Type | Intermittent Explosive Disorder | Familial Male-limited Precocious Puberty | Vascular Cognitive Impairment | Spinocerebellar Ataxia Type 17 | Hemophilia | Dysplastic Nevus | Optic Neuropathy, Anterior Ischemic | X-linked Charcot-Marie-Tooth Disease | Colitis, Microscopic | Polyradiculopathy | Trichorhinophalangeal Syndrome | Fanconi Syndrome | Spinocerebellar Ataxia Type 27 | Diastrophic Dysplasia | Angiosarcoma Of The Breast | Schindler Disease | Hashimoto Thyroiditis | Aspartylglycosaminuria | Neuroectodermal Tumors, Primitive | Branchiootorenal Syndrome | Diabetic Neuropathy | Alopecia Areata | Chronic Thromboembolic Pulmonary Hypertension | Alpha-mannosidosis | Systemic Lupus Erythematosus | Hypohidrotic Ectodermal Dysplasia, X-linked | Interstitial Lung Diseases | Wagner Disease | Infantile Refsum Disease | Polymicrogyria | Epidermal Nevus Syndrome | Gigantism | Isovaleric Acidemia | Asphyxia Neonatorum | Waardenburg Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Colitis | Hemoglobinopathies | Perry Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Niemann-Pick Disease, Type B | Peroxisomal Disorder | DOCK8 Immunodeficiency Syndrome | Hereditary Elliptocytosis | Carbonic Anhydrase VA Deficiency | Aldosteronism | Meier-Gorlin Syndrome | Stiff-man Syndrome | Acute Anterior Uveitis | Diverticulitis | Anti-NMDA Receptor Encephalitis | Osteochondrosis | Retinopathy Of Prematurity | Basan Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Kleine-Levin Syndrome | Triple A Syndrome | Arthritis | Aneurysm, Abdominal Aortic | Lupus Erythematosus | Schizencephaly | Diabetes Mellitus, Transient Neonatal | Stroke, Hemorrhagic | Esthesioneuroblastoma | Basal Cell Nevus Syndrome | Hemimegalencephaly | Vertigo | Sick Sinus Syndrome | Lymphopenia | Thanatophoric Dysplasia Type 1 | Hyperacusis | Facioscapulohumeral Muscular Dystrophy Type 2 | Blepharospasm | Incontinentia Pigmenti | Sickle Cell Disease | Hepatitis | Hyperinsulinemic Hypoglycemia | Lymphoma Lymphoblastic | Facioscapulohumeral Muscular Dystrophy Type 1 | Skin Carcinoma | Rhabdomyosarcoma, Embryonal | Neuromyotonia | Keratopathy | Cryptococcal Meningitis | Photosensitivity | Periventricular Leukomalacia | Eczema | Bethlem Myopathy | Keratitis | Hemorrhage | Pseudohypoaldosteronism | Epidermolysis Bullosa | Autosomal Recessive Spastic Paraplegia Type 35 | Goiter | Myocardial Infarction | Actinomycetoma | Neurocutaneous Syndromes | Avellino Corneal Dystrophy | Pycnodysostosis | Subacute Sclerosing Panencephalitis | Niemann-Pick Disease | Craniopharyngioma | Anemia | Sialidosis Type I | Arthritis, Psoriatic | CHARGE Syndrome | Colitis, Collagenous | Sturge-Weber Syndrome | Osteopathia Striata With Cranial Sclerosis | Hyperferritinemia-cataract Syndrome | Hypersensitivity Pneumonitis | Proteus Syndrome | Pfeiffer Syndrome | Gastritis | Familial Hypertrophic Cardiomyopathy | Spinocerebellar Ataxia Type 2 | MELAS Syndrome | Cataract | Hepatitis, Alcoholic | Osteoglophonic Dysplasia | Panuveitis | Neuroendocrine Cancer | Double Outlet Right Ventricle | Pneumonia, Viral | Hereditary Mixed Polyposis Syndrome | Pancytopenia | Menetrier Disease | Focal Cortical Dysplasia Type 2 | Amelanotic Melanoma | Hepatoblastoma | Polyarteritis Nodosa | Basal Ganglia Disease | Specific Granule Deficiency | Cabezas Syndrome | Spina Bifida | Hyperglycemia | X-linked Sideroblastic Anemia | Multiple Sclerosis, Chronic Progressive | Congenital Torticollis | Mastitis | Glutathione Synthetase Deficiency | Congenital Lipoid Adrenal Hyperplasia | Polyomavirus Nephropathy | Chordoma | Vitelliform Macular Dystrophy | GATA2 Deficiency | Motor Neuron Diseases | Alkaptonuria | Sweet Syndrome | Facioscapulohumeral Muscular Dystrophy | Beare-Stevenson Syndrome | Gestational Trophoblastic Disease | Hepatitis E | Myoclonus-dystonia Syndrome | Microcephalic Primordial Dwarfism | Beta-Propeller Protein-associated Neurodegeneration | ICF Syndrome | Progressive Familial Intrahepatic Cholestasis | Cole-Carpenter Syndrome | Orthostatic Intolerance | Hyperparathyroidism-jaw Tumor Syndrome | Multiple Sulfatase Deficiency | Gaucher Disease | Intestinal Hypomagnesemia 1 | Congenital Absence Of Vas Deferens | Yellow Fever | Spinocerebellar Ataxia Type 38 | Juvenile Myoclonic Epilepsy | Primary Hyperoxaluria Type 1 | Fibrosarcoma | HUPRA Syndrome | Hemorrhagic Disorders | Salla Disease | Hyperparathyroidism, Primary | Ependymoma | Tremor | Ureteropelvic Junction Obstruction | Epithelial-myoepithelial Carcinoma | Waardenburg Syndrome Type 4 | Chronic Leukemia | Depression | Primary Familial Brain Calcification | Tangier Disease | Vertebrobasilar Insufficiency | Juvenile Polyposis | Bietti Crystalline Dystrophy | Granular Corneal Dystrophy Type 1 | Ichthyosis Hystrix, Curth-Macklin Type | Tatton-Brown-Rahman Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Angiomyolipoma | Pneumonia, Bacterial | Osteoarthritis | Pierpont Syndrome | Familial Retinal Arterial Macroaneurysm | Inflammatory Bowel Disease | Medulloblastoma | Mucormycosis | Adrenoleukodystrophy, X-linked | Corneal Dystrophy And Perceptive Deafness | Spinocerebellar Ataxia Type 6 | Anosmia, Congenital | Vascular Calcification | Usher Syndrome | Spinocerebellar Ataxia Type 7 | Babesiosis | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Usher Syndrome Type III | Renal Hypomagnesemia 3 | Myoclonus | Richter's Syndrome | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Rolandic Epilepsy | Esophageal Adenocarcinoma | Mumps | Cryptorchidism | Hypolipoproteinemia | Blastoma, Pleuropulmonary | Carney Triad | Benign Familial Pemphigus | Dysfibrinogenemia | Multiple Sclerosis, Primary Progressive