Disease

Central Pain Syndrome

About the Disease
Central Pain Syndrome, also known as dejerine-roussy syndrome, is related to paine syndrome and spinal cord injury, and has symptoms including chronic pain, acute onset pain and pain, not elsewhere classified. The drugs Pregabalin and Calcium, Dietary have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, brain and cortex.

Common Targets
GNB3

疾病靶点研报
Central Pain Syndrome

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

Other Diseases

Bronchiolitis | Primary Biliary Cholangitis | Congenital Hereditary Endothelial Dystrophy Type II | Basal Ganglia Disease, Biotin-responsive | Autosomal Recessive Bestrophinopathy | Myoclonus | Hypoplastic Left Heart Syndrome | Zimmermann-Laband Syndrome | Rheumatoid Arthritis | Scleroderma, Diffuse | Dystrophy, Cone-rod | Osteonecrosis Of The Jaw | Cancer, Bladder | Pulmonary Vein Stenosis | Familial Hypertrophic Cardiomyopathy | Dyslexia | Cerebral Cavernous Malformations | Pleurisy | Giant Cell Arteritis | Thrombophlebitis | Colitis, Collagenous | Keratocystic Odontogenic Tumor | Intestinal Obstruction | Mandibuloacral Dysplasia With Type A Lipodystrophy | Pigment Dispersion Syndrome | Azoospermia | Osteogenesis Imperfecta Type I | Paronychia | Cutaneous Angiosarcoma | Chloridorrhea, Congenital | Pseudoachondroplasia | Spinocerebellar Ataxia Type 17 | Multiple Sulfatase Deficiency | Non-bullous Congenital Ichthyosiform Erythroderma | Focal Dermal Hypoplasia | Primary Hyperoxaluria | Sleep Apnea, Central | Perivascular Epithelioid Cell Tumor | Osteogenesis Imperfecta Type IV | Acne Vulgaris | Bronchiectasis | Sarcoidosis, Pulmonary | Lattice Corneal Dystrophy | Duane Retraction Syndrome | Microcephaly | Bleeding Disorder Due To CalDAG-GEFI Deficiency | 3-methylglutaconic Aciduria Type IV | Aldosteronism | Mesothelioma, Malignant | Hairy Cell Leukemia | IMAGe Syndrome | Persistent Truncus Arteriosus | Methylmalonic Aciduria And Homocystinuria, CblC Type | Retinoschisis | Hepatoblastoma | Gynecomastia | Cornelia De Lange Syndrome | Hypotonia-cystinuria Syndrome | Rickets | Neuromuscular Disorders | Osteochondrosis | Keratoconjunctivitis | Chronic Periodontitis | Primary Torsion Dystonia | Sepiapterin Reductase Deficiency | Myocardial Infarction | Skin Fragility-woolly Hair Syndrome | Familial Hyperaldosteronism | Dengue Hemorrhagic Fever | Common Cold | Sarcoma, Endometrial Stromal | Hyperparathyroidism-jaw Tumor Syndrome | Crisponi Syndrome | Carey-Fineman-Ziter Syndrome | Retinal Coloboma | Lymphoproliferative Disorders | Hoyeraal-Hreidarsson Syndrome | Krabbe Disease | Spondyloepiphyseal Dysplasia Tarda, X-linked | Chordoid Glioma | Mycosis Fungoides | Goiter, Nodular | Guillain-Barre Syndrome | Sleep Apnea | Myhre Syndrome | Proximal Symphalangism | Glycogen Storage Disease Type 1 | Double Outlet Right Ventricle | Diabetic Macular Edema | Wolfram Syndrome | Osteopetrosis | Chronic Myeloid Leukemia | Epiphyseal Chondrodysplasia, Miura Type | Lymphoma Lymphoblastic | Nager Acrofacial Dysostosis | Ileitis | Spinocerebellar Ataxia Type 7 | Usher Syndrome Type IIC | Hypogammaglobulinemia | DiGeorge Syndrome | Angioedema, Hereditary | Hepatic Adenomatosis | Intestinal Hypomagnesemia 1 | Pneumoconiosis | Aplasia Cutis Congenita | Periventricular Leukomalacia | Cutaneous Mastocytosis | Hyperlipidemia Type V | Usher Syndrome Type III | SAPHO Syndrome | Urolithiasis | Muscle Wasting | Paget's Disease Of The Breast | Ectrodactyly | Spinocerebellar Ataxia Type 10 | Eosinophilia | Ollier Disease | Moyamoya Disease | Spinal And Bulbar Muscular Atrophy | Adenosine Deaminase 2 Deficiency | Trichomegaly | TARP Syndrome | Hyper IgE Syndrome | Bietti Crystalline Dystrophy | Proopiomelanocortin Deficiency | Chronic Kidney Disease | Generalized Epilepsy And Paroxysmal Dyskinesia | Still Disease | Syphilis | Pyloric Stenosis, Infantile Hypertrophic | Acute Myeloid Leukemia | Synpolydactyly | Homocystinuria | Leiomyoma | Disseminated Intravascular Coagulation | Bardet-Biedl Syndrome | Blepharophimosis Syndrome | Tinea | Hemosiderosis | Lipodystrophy | Vitelliform Macular Dystrophy | Angina Pectoris | Cerebrotendinous Xanthomatosis | Glycogen Storage Disease Type 9 | Epidermodysplasia Verruciformis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Pseudohypoparathyroidism Type 2 | Congenital Disorders Of Glycosylation Type II | Hyperinsulinism-hyperammonemia Syndrome | Osteochondroma | Transcobalamin Deficiency | Martsolf Syndrome | Otopalatodigital Syndrome Type 2 | Campomelic Dysplasia | Oculopharyngeal Muscular Dystrophy | Non-epidermolytic Palmoplantar Keratoderma | Waardenburg Syndrome Type 2E | Systemic Lupus Erythematosus | Fibrosarcoma | Chondrodysplasia Punctata | Spondylosis | Chylomicron Retention Disease | Congenital Stromal Corneal Dystrophy | Marfan Syndrome | Non-Hodgkin Lymphoma | Echinococcosis | Pontocerebellar Hypoplasia Type 2 | Early Infantile Epileptic Encephalopathy 1 | Pemphigus Foliaceus | Spinal Cord Diseases | Multiple Sclerosis, Chronic Progressive | VACTERL Association | Hyperekplexia | 3-methylcrotonyl-CoA Carboxylase Deficiency | Inflammatory Myofibroblastic Tumor | Mitochondrial Myopathy | Chanarin-Dorfman Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | X-linked Sideroblastic Anemia | Autoimmune Polyendocrinopathy Syndrome Type I | Liver Failure | Raine Syndrome | Trichorhinophalangeal Syndrome | Cat Eye Syndrome | Rhabdomyosarcoma | Epilepsy | Chudley-McCullough Syndrome | Diarrhea | Mixed Connective Tissue Disease | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Orthostatic Intolerance | Polycystic Kidney, Autosomal Recessive | Perry Syndrome | Corneal Edema | Influenza | DNA Ligase IV Deficiency | Inflammatory Linear Verrucous Epidermal Nevus | Metanephric Adenoma | Sturge-Weber Syndrome | Dermatitis | Pericarditis | Waardenburg Syndrome Type 2A | Thrombocythemia, Essential | Fetal And Neonatal Alloimmune Thrombocytopenia | Dysgerminoma | Creatine Deficiency Syndrome | Fascioliasis | Retinitis Pigmentosa 3 | Charcot-Marie-Tooth Disease Type 4B1 | Schuurs-Hoeijmakers Syndrome | Charcot-Marie-Tooth Disease, Type 6 | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Abetalipoproteinemia | Medulloblastoma | Nephropathy | Hemorrhoids | Hyperkeratosis | Congenital Hemolytic Anemia | Mucolipidosis | Chronic Lymphocytic Leukemia | Pheochromocytoma | Microcephalic Primordial Dwarfism | Wagner Disease | Williams Syndrome | Aneurysm, Abdominal Aortic | Leukoplakia, Oral | Glutaric Aciduria Type 2 | Pachyonychia Congenita | Dementia | High Molecular Weight Kininogen Deficiency | CDKL5 Deficiency Disorder | Colorectal Adenoma | Distal Myopathy 2 | Intestinal Tuberculosis | Congenital Myasthenic Syndrome | Spinocerebellar Ataxia Type 3 | Leber Congenital Amaurosis | Congenital Aniridia | Hypersensitivity | Fontaine Progeroid Syndrome | Tardive Dyskinesia | Fibronectin Glomerulopathy | Mucolipidosis Type IV | Vitamin B12 Deficiency | N-acetylglutamate Synthase Deficiency | Acrocallosal Syndrome | Lymphedema | Ataxia-ocular Apraxia 2 | Vulvovaginitis | Atrial Septal Defect | Dubin-Johnson Syndrome | Episodic Ataxia Type 1 | Atopy | Hypercholesterolemia, Familial | Metachromatic Leukodystrophy | Meniere's Disease | Endometriosis | Evans Syndrome | Pseudohypoaldosteronism | Esophageal Adenocarcinoma | Inflammatory Joint Disease | Partington Syndrome | Transient Bullous Dermolysis Of The Newborn | Hereditary Multiple Exostoses | Primary Ovarian Insufficiency | Eclampsia | Erythrokeratodermia Variabilis | Myotonia | Cholestasis, Intrahepatic | Myotonic Disorders | Renal Dysplasia | Primary Cutaneous Amyloidosis | Autoimmune Hemolytic Anemia | Glycogen Storage Disease Type 5 | Familial Mediterranean Fever | Meningioma | Vertigo | Scoliosis | Pelizaeus-Merzbacher Disease | Retinal Diseases | Malonyl-CoA Decarboxylase Deficiency | Hemolytic Uremic Syndrome, Atypical | Cold Agglutinin Disease | Acne | Isobutyryl-CoA Dehydrogenase Deficiency | Celiac Disease | Pulmonary Sclerosing Hemangioma | Motion Sickness | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Amblyopia | Hemorrhagic Disorders | Cellulitis | Neurocysticercosis | Frontotemporal Dementia | Chronic Idiopathic Myelofibrosis | Cardiofaciocutaneous Syndrome | Swine Influenza | Sporadic Hemiplegic Migraine | Congenital Muscular Dystrophy | Hypospadias | Sarcoma, Ewing | Endometrial Hyperplasia | Optic Nerve Diseases | Dysferlinopathy | Acute Chest Syndrome | PASLI Disease | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Twin-to-twin Transfusion Syndrome | Extramammary Paget's Disease | Cholelithiasis | Keloid | Kernicterus | Chronic Neutrophilic Leukemia | Glucagonoma | Craniometaphyseal Dysplasia | Supravalvular Aortic Stenosis | Obesity | Sweet Syndrome | Schizophrenia | Keratitis-ichthyosis-deafness Syndrome | Niemann-Pick Disease, Type A | Ovarian Sex Cord-stromal Tumor | Placenta Previa | Sickle Cell Anemia | Tibial Muscular Dystrophy | Lymphoproliferative Disease, X-linked | Bone Giant Cell Tumor | Brenner Tumor | Histiocytic Sarcoma | Waardenburg Syndrome Type 1 | Spinocerebellar Ataxia Type 6 | Trigonocephaly | Enterocolitis, Necrotizing | Mumps | Teratozoospermia | Optic Nerve Hypoplasia, Bilateral | CHARGE Syndrome | Avellino Corneal Dystrophy | Brugada Syndrome 1 | Achondrogenesis | Astigmatism | Dyslipidemia | Glaucoma | Pancreatitis | Lymphoma, Follicular | Muscular Dystrophy | Congenital Dyserythropoietic Anemia Type 1 | Giant Cell Glioblastoma | Scapuloperoneal Myopathy, X-linked Dominant | Pyoderma Gangrenosum | Vestibular Disease | Beta-Propeller Protein-associated Neurodegeneration | Hydrocephalus, Normal Pressure | Benign Familial Infantile Seizures | Erythropoietic Protoporphyria | Lipoma | ACTH-independent Macronodular Adrenal Hyperplasia | Carcinoma, Transitional Cell | Gangliosidosis, GM1 | Chronic Myelomonocytic Leukemia | Facioscapulohumeral Muscular Dystrophy | Glycogen Storage Disease Type 0, Muscle | Hypertensive Retinopathy | Galactosemia | Lymphomatoid Granulomatosis | Acute Lung Injury | Endometritis | Myelomeningocele | Epidermolytic Palmoplantar Keratoderma | Sensory Neuropathy | Ocular Hypertension | Thyroid Hormone Resistance | Aceruloplasminemia | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Neurofibromatosis Type 1 | Snyder-Robinson Syndrome | Bursitis | Peritonitis | Sclerosteosis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Calcium Pyrophosphate Deposition Disease | Feingold Syndrome | Benign Familial Neonatal Convulsions | Larsen Syndrome | Peripheral T-cell Lymphoma | Axenfeld-Rieger Syndrome | Familial Advanced Sleep Phase Syndrome | Pitt-Hopkins Syndrome | Priapism | Schamberg Disease | Prediabetes | Constipation | Familial Partial Lipodystrophy | Fuchs Dystrophy | Burn-McKeown Syndrome | Fabry's Disease | Adult Polyglucosan Body Disease | Stickler Syndrome | Tay-Sachs Disease | Wiedemann-Steiner Syndrome