Dystonia-parkinsonism, X-linked
Dystonia-parkinsonism, X-linked
About the Disease
Dystonia 3, Torsion, X-Linked, also known as x-linked dystonia-parkinsonism, is related to dystonia 1, torsion, autosomal dominant and dystonia 12, and has symptoms including dystonia, myoclonus and torticollis. An important gene associated with Dystonia 3, Torsion, X-Linked is TAF1 (TATA-Box Binding Protein Associated Factor 1), and among its related pathways/superpathways are RNA Polymerase II Transcription Initiation And Promoter Clearance and HIV Life Cycle. The drugs Mung bean and Botulinum Toxins have been mentioned in the context of this disorder. Affiliated tissues include caudate nucleus, tongue and eye, and related phenotypes are chorea and myoclonus
Common Targets
PLA2G6 | PRKRA | PARK7

Note: If you'd like to get a target analysis report for Dystonia-parkinsonism, X-linked, 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 Dystonia-parkinsonism, X-linked at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Inflammatory Bowel Disease | Amish Infantile Epilepsy Syndrome | Pulmonary Alveolar Microlithiasis | Clouston Hidrotic Ectodermal Dysplasia | Neurocutaneous Melanocytosis | Non-Langerhans Cell Histiocytosis | Restrictive Dermopathy | Tenosynovial Giant Cell Tumor | Leukoplakia | Epidermolysis Bullosa | Polycystic Ovary Syndrome | Myocarditis | Postaxial Polydactyly | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Cholestasis, Intrahepatic | Gingivitis | Encephalocele | Adenosine Deaminase 2 Deficiency | Primrose Syndrome | Distal Myopathy 2 | Acromicric Dysplasia | Lymphomatoid Granulomatosis | Spinocerebellar Ataxia Type 27 | Lennox-Gastaut Syndrome | Thrombosis | Branchiootorenal Syndrome | Myotonic Disorders | Occipital Neuralgia | Stroke, Hemorrhagic | Esophageal Motility Disorders | Glycogen Storage Disease Type 3 | Presbycusis | Parvovirus B19 Infection | Progressive Osseous Heteroplasia | Osteoporosis-pseudoglioma Syndrome | Photosensitivity | Pure Autonomic Failure | Hemochromatosis Type 2 | DRESS Syndrome | Hernia, Inguinal | Von Hippel-Lindau Disease | Enterocolitis, Necrotizing | Hypotrichosis Simplex | Guillain-Barre Syndrome | Posterior Polar Cataract | Alopecia | Waardenburg Syndrome Type 2A | Canavan Disease | Melanoma, Malignant | Bronchitis | Azoospermia | Keratitis | AIDS | Corneal Dystrophies, Hereditary | Synpolydactyly | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Frank-ter Haar Syndrome | Hypolipoproteinemia | Pelizaeus-Merzbacher Disease | Non-bullous Congenital Ichthyosiform Erythroderma | Pontocerebellar Hypoplasia | Glycogen Storage Disease Type 1a | Osteochondroma | Smoldering Myeloma | Pineoblastoma | Intestinal Tuberculosis | Retinal Vasculitis | Cysticercosis | Tetraplegia | Fowler's Syndrome | Double Outlet Right Ventricle | Hepatitis, Alcoholic | Cyclic Vomiting Syndrome | Hepatitis, Chronic | Urofacial Syndrome | Presbyopia | Hyperbilirubinemia | Meningococcal Meningitis | Vitreoretinal Degeneration, Snowflake Type | Hydrolethalus Syndrome | Motor Neuron Diseases | Glomerulonephritis, Membranoproliferative | Proopiomelanocortin Deficiency | Spinal Cord Diseases | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Niemann-Pick Disease, Type A | Sialoadenitis | Hypermetropia | Bernard-Soulier Syndrome | Olmsted Syndrome | Epithelioid Hemangioma | Hypertension | Non-proliferative Diabetic Retinopathy | Goiter | Brachydactyly | Galloway-Mowat Syndrome | Angina Pectoris | Chorea | Thyroiditis, Autoimmune | Adenoid Cystic Carcinoma | Keratoconus | Hypokalemic Periodic Paralysis | Persistent Fetal Circulation | 3C Syndrome | Osteogenesis Imperfecta Type I | Aldosteronism | Ocular Surface Squamous Neoplasia | Agnathia-Otocephaly Complex | Oculocutaneous Albinism | Neurodevelopmental Disorders | Eosinophilia | Spinocerebellar Ataxia Type 2 | Preaxial Polydactyly | Analgesia | Chorea-acanthocytosis | Myoclonus-dystonia Syndrome | Endometrial Hyperplasia | Zimmermann-Laband Syndrome | Choroideremia | Pancytopenia | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Oral Lichen Planus | Seasonal Mood Disorder | Beare-Stevenson Syndrome | Sweet Syndrome | Hyperparathyroidism, Secondary | Recurrent Respiratory Papillomatosis | Hereditary Hemorrhagic Telangiectasia | Hepatitis D | Pantothenate Kinase-associated Neurodegeneration | Corneal Dystrophy | Arthritis, Gouty | Retinal Diseases | Craniolenticulosutural Dysplasia | Neuronal Ceroid Lipofuscinosis | Genee-Wiedemann Syndrome | Huntington's Disease | Hemolytic Uremic Syndrome, Atypical | Vitamin K Deficiency | Transient Bullous Dermolysis Of The Newborn | Cyst | Congenital Mirror Movements | Alazami Syndrome | Macular Degeneration | Postpoliomyelitis Syndrome | Charcot-Marie-Tooth Disease Type 2T | Otitis Externa | Jalili Syndrome | Multiple Sulfatase Deficiency | Isovaleric Acidemia | Mycosis Fungoides | Birt-Hogg-Dube Syndrome | Hyperammonemia | Synovitis | Polyomavirus Nephropathy | Retinitis | Mucolipidosis | Acanthosis Nigricans | Tetanus | Hypoglycemia | Palmoplantar Keratoderma | Congenital Fiber-type Disproportion Myopathy | Binge Eating Disorder | Pulmonary Sclerosing Hemangioma | Trigonocephaly | Papilledema | Episodic Ataxia Type 1 | Thromboembolism | Skin Fragility-woolly Hair Syndrome | Thanatophoric Dysplasia Type 1 | Hypertrophy | Gerodermia Osteodysplastica | SAPHO Syndrome | Glomerulonephritis, Membranous | Chronic Enteropathy Associated With SLCO2A1 Gene | Yellow Fever | Aicardi-Goutieres Syndrome | Fascioliasis | Oculocutaneous Albinism Type 4 | Congenital Central Hypoventilation Syndrome | Poikiloderma With Neutropenia | Plasmacytoma | Rhizomelic Chondrodysplasia Punctata | Adenylosuccinate Lyase Deficiency | Patent Foramen Ovale | Sclerosteosis | Cataract | Diffuse Intrinsic Pontine Glioma | Goiter, Nodular | Amebiasis | Cleidocranial Dysplasia | Dental Caries | Hypoalbuminemia | Glycogen Storage Disease Type 1b | Autoimmune Disease | Spinal And Bulbar Muscular Atrophy | Oligoastrocytoma | Ileitis | Dysequilibrium Syndrome | Pulmonary Vein Stenosis | Retinopathy, Diabetic | Mucolipidosis Type II | Fibromyalgia | Osteogenesis Imperfecta Type II | Hemolytic Anemia | Acrocallosal Syndrome | Persistent Truncus Arteriosus | Chondrosarcoma | Blepharospasm | Histiocytosis | Cholangiocarcinoma | Primary Hyperoxaluria Type 1 | Thyroid Hormone Resistance | Fetal Alcohol Syndrome | Rhabdomyosarcoma, Alveolar | Epilepsy, Generalized | Uveitis | VEXAS Syndrome | Lung Diseases | Stuve-Wiedemann Syndrome | Diabetic Encephalopathy | Fibrosis | Aldosterone Deficiency | Veno-occlusive Disease | Dyslipidemia | Norrie Disease | Multiple Hamartoma Syndrome | Lichen Sclerosus | Narcolepsy | Fahr Disease | Hepatitis | Thrombophilia | Spasticity | Vulvovaginitis | Agammaglobulinemia | Glioblastoma | Pseudohypoparathyroidism Type 1A | Lupus Erythematosus | Hashimoto Thyroiditis | Leiomyoma | Axenfeld-Rieger Syndrome | Otitis Media | Retinal Telangiectasia | Vitamin B12 Deficiency | Wolman Disease | Seminoma | Tyrosinemia Type 2 | GNE Myopathy | Burn-McKeown Syndrome | Cerebellar Ataxia, Cayman Type | Mandibuloacral Dysplasia With Type A Lipodystrophy | Ocular Hypertension | VACTERL/VATER Association | Hypothalamic Obesity | Cancer, Kidney | Xeroderma Pigmentosum Variant Type | Chromosome 5q Deletion Syndrome | Leber Congenital Amaurosis | Nevus | Nicotine Dependence | Charcot-Marie-Tooth Disease, Type 1A | Glutathione Synthetase Deficiency | Crouzon Syndrome With Acanthosis Nigricans | Lymphoma, AIDS-related | Acrodysostosis | Hypotonia-cystinuria Syndrome | Holoprosencephaly | Neuroma | Trimethylaminuria | Thanatophoric Dysplasia | Retinal Detachment | Castleman Disease | Keratosis | Splenomegaly | Kearns-Sayre Syndrome | Periventricular Nodular Heterotopia | Intestinal Pseudo-obstruction | Primary Carnitine Deficiency | Subcortical Band Heterotopia | Anti-NMDA Receptor Encephalitis | Ganglioglioma | Hyperlipidemia, Familial Combined | Sleep Apnea, Central | Tricho-hepato-enteric Syndrome | Autoimmune Autonomic Ganglionopathy | Antithrombin III Deficiency | Greenberg Dysplasia | Retinitis Pigmentosa 3 | Mucolipidosis Type III | Hidradenitis Suppurativa | Gastritis, Atrophic | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Usher Syndrome Type III | High Molecular Weight Kininogen Deficiency | Scleroderma, Diffuse | Myopia | 3-methylglutaconic Aciduria Type IV | Diverticulitis | Ehlers-Danlos Syndrome | Shprintzen-Goldberg Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Cardiomyopathy, Dilated, 1L | Multicentric Carpotarsal Osteolysis Syndrome | Williams Syndrome | Usher Syndrome | Myofibromatosis | Melanoma, Uveal | Diabetes Mellitus, Transient Neonatal | Anovulation | Botulism | Hypertensive Nephropathy | Idiopathic Pulmonary Fibrosis | Pneumothorax | Basal Cell Nevus Syndrome | Motion Sickness | Marinesco-Sjogren Syndrome | Omenn Syndrome | Focal Cortical Dysplasia Type 2 | Cold Agglutinin Disease | Triple A Syndrome | Meleda Disease | Hepatitis E | Acute Chest Syndrome | Tendinopathy | Primary Familial Brain Calcification | Optic Neuritis | Klinefelter Syndrome | Mountain Sickness | Adenocarcinoma | Osteonecrosis Of The Jaw | Hereditary Elliptocytosis | Dysmorphophobia | Cutaneous Lupus Erythematosus | Charcot-Marie-Tooth Disease Type 4D | Esophagitis | Premature Ejaculation | Craniosynostosis | Juvenile Myoclonic Epilepsy | Esophageal Carcinoma | Obesity, Morbid | Benign Recurrent Intrahepatic Cholestasis 1 | Hemangioblastoma | Paraplegia | GATA2 Deficiency | Prolidase Deficiency | Retinoblastoma | Bainbridge-Ropers Syndrome | Chronic Leukemia | Juvenile Myelomonocytic Leukemia | Schizencephaly | Metatropic Dysplasia | Spinocerebellar Ataxia Type 28 | Cole-Carpenter Syndrome | Fraser Syndrome | Thrombophlebitis | Epiphyseal Chondrodysplasia, Miura Type | Pneumococcal Meningitis | Keratopathy | Otosclerosis | Hepatoblastoma | Phenylketonuria | Lymphangioleiomyomatosis | Charcot-Marie-Tooth Disease Type 2D | Palsy, Cerebral | Leukemia-lymphoma, Adult T-cell | Desbuquois Syndrome | Cystinuria | Congenital Tufting Enteropathy | Chronic Thromboembolic Pulmonary Hypertension | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Nail-Patella Syndrome | HIBCH Deficiency | Anosmia, Congenital | Glycogen Storage Disease Type 4 | Intellectual Disability, Autosomal Dominant 5 | Keratosis, Seborrheic | Gilbert Syndrome | Diamond-Blackfan Anemia | Arrhythmogenic Right Ventricular Cardiomyopathy | Cornelia De Lange Syndrome | Vitiligo | Congenital Heart Block | Amblyopia | Angiomyolipoma | Trichomegaly | Schistosomiasis Mansoni | Cholangitis | Placenta Previa | Pulmonary Veno-occlusive Disease | Batten Disease | Spina Bifida | Brugada Syndrome 1 | Tic Disorder | Alstrom Syndrome | Episodic Ataxia | Ovarian Sex Cord-stromal Tumor | Xeroderma Pigmentosum | Polycythemia | Schamberg Disease | Asthma