Disease

Spasticity

About the Disease
Spasticity is related to spastic paraplegia 41, autosomal dominant and spastic paraplegia 19, autosomal dominant. An important gene associated with Spasticity is SPAST (Spastin), and among its related pathways/superpathways is Sudden infant death syndrome (SIDS) susceptibility pathways. The drugs Memantine and Dopamine have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, brain and skeletal muscle, and related phenotypes are nervous system and growth/size/body region

Common Targets
Alpha-2 Adrenergic receptors (nonspecified subtype) | HTR1A | Nicotinic alpha4beta2alpha5 Receptor | Kainate Receptor (GluR) (nonspecified subtype) | GABA(A) receptor | Gamma-Aminobutyric acid type B receptor | Voltage-Gated Sodium Channel Complex | MGLL | KCNQ3 | Sodium channel (nonspecified subtype) | SCN3A | TRPV2 | G1/S-specific cyclin-E (nonspecified subtype) | SCN8A | CHRNA7 | Guanylate cyclase (nonspecified subtype) | SLC6A9 | OPRD1 | Nicotinic alpha4beta2 receptor | SCN4A | Myosin Class II (nonspecified subtype) | NMDA receptor | TRPA1 | PTGDR2 | GABRA1 | MYH2 | SCN9A | EXOSC3 | CCNE1 | SCN1A | Muscarinic Acetylcholine Receptor (mAChR) (nonspecified subtype) | 5-Hydroxytryptamine Receptor 2 (5-HT2) (nonspecified subtype) | Glycine receptor | SLC2A1 | Cannabinoid receptor (nonspecified subtype) | Large Conductance BK(Ca) Potassium Channel (Maxi K+ Channel) (nonspecified subtype) | GPR55 | SCN5A | MAOB | GABRA2 | CDK2/Cyclin E | G595 | OPRM1 | CHRNB2 | Neuronal acetylcholine receptor alpha2beta2 receptor | ABAT | CNR2 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | KCNQ2 | SCN2A | Glutamate Receptor Ionotropic AMPA Receptor | Calcium channel (nonspecified subtype) | CDK2 | CDK4 | SLC6A5 | SCN10A | 5-Hydroxytryptamine Receptor 3 (5-HT3 receptor) (nonspecified subtype) | Nicotinic alpha1beta1deltaepsilon Receptor | CDK4/Cyclin D1 | Protein kinase C (nonspecified subtype) | TRPM8 | CNR1 | MAOA | TRPV1

疾病靶点研报
Spasticity

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

Other Diseases

Diabetes | Porphyria, Variegate | Bietti Crystalline Dystrophy | Neurocysticercosis | Posterior Polar Cataract | Trachoma | Osteonecrosis Of The Jaw | Neuromyelitis Optica | Paraplegia | Hartsfield Syndrome | Lennox-Gastaut Syndrome | Leukocyte Adhesion Deficiency | Pierre Robin Syndrome | Thrombophilia | Ehlers-Danlos Syndrome | Charcot-Marie-Tooth Disease Axonal Type 2N | Holt-Oram Syndrome | Adenosine Deaminase Deficiency | Peeling Skin Syndrome Type B | Cat Eye Syndrome | Hepatitis, Autoimmune | Retinal Coloboma | Seminoma | Low Tension Glaucoma | Primary Erythromelalgia | Pneumonia, Mycoplasma | Thanatophoric Dysplasia Type 1 | Porphyria Cutanea Tarda | Fahr Disease | Chylothorax, Congenital | Axenfeld-Rieger Syndrome | Martsolf Syndrome | Fibrosis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Tendinitis | Lattice Corneal Dystrophy Type 1 | Scleroderma | Astrocytoma, Anaplastic | Sweet Syndrome | Hyperostosis | Colitis, Microscopic | Arteriosclerosis | Tylosis With Esophageal Cancer | Usher Syndrome Type I | Systemic Lupus Erythematosus | Pancreatitis, Chronic | Meconium Ileus | Dystonia | Adenoma, Pleomorphic | Arts Syndrome | Sleep Apnea | Hereditary Pyropoikilocytosis | Urolithiasis | Charcot-Marie-Tooth Disease Type 4E | Trigonocephaly | Cancer, Bladder | Spinocerebellar Ataxia Type 27 | Leber Hereditary Optic Neuropathy | Cornelia De Lange Syndrome | Encephalopathy, Hepatic | Schizophrenia, Paranoid | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Trimethylaminuria | Nanophthalmos | Pain | Anthrax | Hyperthermia, Malignant | Colitis, Collagenous | Generalized Epilepsy With Febrile Seizures Plus | Neural Tube Defect | Dysthymia | Marfan Syndrome | Hepatitis E | Epithelioid Hemangioma | Hereditary Sensory And Autonomic Neuropathy | Macrophagic Myofasciitis | Pleural Tuberculosis | Nephrocalcinosis | Salla Disease | Miyoshi Myopathy | Coloboma | Pyloric Stenosis, Infantile Hypertrophic | Vitiligo | ICF Syndrome | Pyelonephritis | Ganglioglioma | Phenylketonuria II | Dupuytren Disease | Asthma | Hypoalbuminemia | Spinocerebellar Ataxia Type 17 | B-cell Prolymphocytic Leukemia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Neuroleptic Malignant Syndrome | Basal Ganglia Cerebrovascular Disease | Dementia | Meningioma | Fibrosarcoma | Aromatic L-amino Acid Decarboxylase Deficiency | Palsy, Cerebral | Corneal Dystrophy And Perceptive Deafness | Nail-Patella Syndrome | Hemolytic Uremic Syndrome, Atypical | Spinocerebellar Ataxia Type 42 | Klinefelter Syndrome | Asphyxia Neonatorum | Congenital Generalized Lipodystrophy | Vitreoretinopathy, Proliferative | C3 Glomerulonephritis | Triple A Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Niemann-Pick Disease, Type A | Adrenal Insufficiency | Polyarteritis Nodosa | Hyperacusis | Molybdenum Cofactor Deficiency | Campomelic Dysplasia | Orthostatic Intolerance | Costello Syndrome | Congenital Absence Of Vas Deferens | Cousin Syndrome | Vici Syndrome | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Okihiro Syndrome | Skin Carcinoma | Corneal Ulcer | Leukoplakia | Aphasia | Tumoral Calcinosis | Kabuki Syndrome 2 | Peroxisomal Disorder | Scapuloperoneal Spinal Muscular Atrophy | Esthesioneuroblastoma | Osteosarcoma | Babesiosis | Duodenal Atresia | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Chronic Kidney Disease | Alcoholism | Lassa Fever | Sclerocornea | Renal Oncocytoma | Hyperferritinemia-cataract Syndrome | Cholestasis | Shock, Cardiogenic | Hypopigmentation | Wolfram Syndrome | Gingivitis | Encephalopathy | DEND Syndrome | Specific Granule Deficiency | Hypertriglyceridemia | Osteogenesis Imperfecta Type IV | Anterior Segment Dysgenesis | Eccrine Porocarcinoma | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Syphilis | Carbamoyl Phosphate Synthetase I Deficiency | Hereditary Spherocytosis | Pemphigus | Pseudohypoaldosteronism | Hyperbilirubinemia, Neonatal | Combined Malonic And Methylmalonic Acidemia | Toxoplasmosis | Sickle Cell Disease | Hereditary Hemorrhagic Telangiectasia Type 2 | Fragile X Syndrome | Preaxial Polydactyly | Congenital Myasthenic Syndrome | Fontaine Progeroid Syndrome | Wagner Disease | Cholera | Charcot-Marie-Tooth Disease, Type 2C | Haim-Munk Syndrome | Erectile Dysfunction | Charcot-Marie-Tooth Disease Type 3 | Pleurisy | Silicosis | Delayed Sleep Phase Syndrome | Blue Nevus | Proopiomelanocortin Deficiency | Hoyeraal-Hreidarsson Syndrome | Osteogenesis Imperfecta Type VI | Micro Syndrome | Pontocerebellar Hypoplasia | Myelitis, Transverse | Epithelial-myoepithelial Carcinoma | Interstitial Lung Diseases | Mycosis Fungoides | Kashin-Beck Disease | Meesmann Corneal Dystrophy | Blomstrand Osteochondrodysplasia | Goiter | Spinocerebellar Ataxia Type 2 | Bone Giant Cell Tumor | Amblyopia | Greig Cephalopolysyndactyly Syndrome | Arthritis, Reactive | Colon Adenoma | CHOPS Syndrome | Tyrosine Hydroxylase Deficiency | Congenital Bile Acid Synthesis Defect | Schwartz-Jampel-Aberfeld Syndrome | Schnitzler Syndrome | Anosmia, Congenital | Binge Eating Disorder | Osteopetrosis | Osteogenesis Imperfecta Type III | Schizotypal Personality Disorder | Diffuse Mesangial Sclerosis | Fetal And Neonatal Alloimmune Thrombocytopenia | Hartnup Disease | Non-proliferative Diabetic Retinopathy | Wolman Disease | Aldosterone Synthase Deficiency | Paraganglioma, Carotid Body | Otopalatodigital Syndrome Type 2 | Dysplastic Nevus | Schistosomiasis | Cellulitis | Deafness, Dystonia, And Cerebral Hypomyelination | Alexander Disease | Creatine Deficiency Syndrome Due To AGAT Deficiency | Chronic Idiopathic Myelofibrosis | Zellweger Syndrome | Neurodegeneration With Brain Iron Accumulation | Benign Familial Pemphigus | Renal Failure | Fowler's Syndrome | Cyclic Vomiting Syndrome | Primary Carnitine Deficiency | Hypertelorism | Aldosterone Deficiency | Prune Belly Syndrome | Gilbert Syndrome | Rhabdoid Tumor | Persistent Truncus Arteriosus | Encephalitis | Facioscapulohumeral Muscular Dystrophy Type 1 | Spondyloepiphyseal Dysplasia Tarda, X-linked | Cenani-Lenz Syndactyly Syndrome | Mitochondrial Cytopathy | Pseudomyxoma Peritonei | Myoclonic Epilepsy With Ragged Red Fibers | Encephalitis, Tick-borne | Riboflavin Transporter Deficiency Neuronopathy | X-linked Charcot-Marie-Tooth Disease | Goiter, Nodular | Peeling Skin Syndrome, Acral Type | Congenital Heart Block | Proximal Symphalangism | Episodic Ataxia | Spinocerebellar Ataxia Type 15 | Joubert Syndrome | Wiskott-Aldrich Syndrome | LRBA Deficiency | Sick Sinus Syndrome | Inflammatory Myofibroblastic Tumor | Sarcoma, Ewing | Stroke | Sjogren Syndrome | Torticollis | Nephroblastoma | Hepatic Adenomatosis | Keratosis, Actinic | Spinocerebellar Ataxia Type 10 | Sclerosteosis 2 | Polycystic Ovary Syndrome | Gestational Trophoblastic Disease | Chronic Myelomonocytic Leukemia | Congenital Primary Aphakia | Mitochondrial Encephalomyopathy | Viral Meningitis | Fuchs Heterochromic Iridocyclitis | AIDS | Mannosidase Deficiency Diseases | Carey-Fineman-Ziter Syndrome | Olmsted Syndrome | Cranioectodermal Dysplasia | Proteasome-associated Autoinflammatory Syndrome 2 | Subcortical Band Heterotopia | Panuveitis | Spinocerebellar Ataxia Type 28 | Dengue Hemorrhagic Fever | Japanese Encephalitis | Hepatitis A | Tinea | Hepatic Veno-occlusive Disease | Impulse Control Disorder | Nephropathy | Dystrophy, Cone-rod | Polyneuropathy | Exfoliative Dermatitis | Acral Lentiginous Melanoma | Succinic Semialdehyde Dehydrogenase Deficiency | Presbycusis | Pregnancy, Ectopic | Achondrogenesis | Loeys-Dietz Syndrome Type 4 | Arterial Tortuosity Syndrome | Glutaric Aciduria Type 2 | Pernicious Anemia | Acanthosis Nigricans | Achromatopsia | GM2-gangliosidosis AB Variant | Persistent Fetal Circulation | GAPO Syndrome | Anorexia Nervosa | Smith-Kingsmore Syndrome | Kearns-Sayre Syndrome | Asperger Syndrome | Long QT Syndrome Type 2 | Ellis-Van Creveld Syndrome | Pouchitis | Cancer, Prostate | Episodic Ataxia Type 1 | Hypertension, Pulmonary | Leukemia-lymphoma, Adult T-cell | Best Macular Dystrophy | Tardive Dyskinesia | Pyruvate Kinase Deficiency | Communication Disorders | Alpers Syndrome | Tay-Sachs Disease | Pseudohypoparathyroidism Type 2 | Acute Generalized Exanthematous Pustulosis | Eczema | Adrenoleukodystrophy, X-linked | Iron Deficiency Anemia | Primary Progressive Nonfluent Aphasia | Neuroectodermal Tumors, Primitive | Zollinger-Ellison Syndrome | Cryopyrin-associated Periodic Syndromes | Microvillus Inclusion Disease | Hemolytic Anemia | Tendinopathy | Postpartum Depression | Kawasaki Disease | Pneumococcal Meningitis | Hyperinsulinemic Hypoglycemia | Tracheal Disorders | Migraine | Dyggve-Melchior-Clausen Disease | Distal Myopathy | Ichthyosis Bullosa Of Siemens | Myotonic Disorders | Progressive Myoclonic Epilepsy | Danon Disease | Periodontitis | Traboulsi Syndrome | Sezary Syndrome | Filariasis | Congenital Dyserythropoietic Anemia | Oligodendroglioma | Angioedema, Hereditary | Trichorhinophalangeal Syndrome | Smoldering Myeloma | Alazami Syndrome | Frank-ter Haar Syndrome | Precocious Puberty | Sturge-Weber Syndrome | Ectodermal Dysplasia | Sporadic Inclusion Body Myositis | B-cell Chronic Lymphocytic Leukemia | Meningeal Melanocytoma | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Hairy Cell Leukemia | Mastitis | Myhre Syndrome | Ollier Disease | Spondylocostal Dysostosis | Fascioliasis | Non-Hodgkin Lymphoma | Tyrosinemia Type 2 | Antenatal Bartter Syndrome Type 1 | Hyperthyroidism | Aceruloplasminemia | Erythrokeratodermia Variabilis | Peripheral T-cell Lymphoma | Charcot-Marie-Tooth Disease Type 2E | Bainbridge-Ropers Syndrome | Asthma, Nocturnal | Papilledema | Oculodentodigital Dysplasia | Crimean-Congo Hemorrhagic Fever | Hidradenitis Suppurativa | Gaucher Disease | Gerodermia Osteodysplastica | Ameloblastic Carcinoma | Hyperkeratosis | Keratopathy | Congenital Nephrotic Syndrome | Lamellar Ichthyosis | Prediabetes | Brachydactyly | High Molecular Weight Kininogen Deficiency | Meningococcal Infections | Cholangitis | Pre-eclampsia | Richter's Syndrome