Disease

Pure Autonomic Failure

About the Disease
Pure Autonomic Failure, also known as orthostatic hypotension, is related to multiple system atrophy 1 and dementia, lewy body. An important gene associated with Pure Autonomic Failure is DBH (Dopamine Beta-Hydroxylase), and among its related pathways/superpathways are Neuroscience and superpathway of tryptophan utilization. The drugs Droxidopa and Norepinephrine have been mentioned in the context of this disorder. Affiliated tissues include spinal cord, heart and brain, and related phenotypes are orthostatic hypotension and anhidrosis

Common Targets
LAG3 | G5133 | GRIN2B | Major histocompatibility complex class II antigens (nonspecified subtype) | FGL1

疾病靶点研报
Pure Autonomic Failure

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

Other Diseases

Neurofibrosarcoma | Cannabis Abuse | Gastric Atrophy | ICF Syndrome | Unverricht-Lundborg Syndrome | Urticaria | Vitamin A Deficiency | Epidermolysis Bullosa Dystrophica | Obesity, Morbid | Hypertrophy | Venous Insufficiency | Craniometaphyseal Dysplasia | Progressive Familial Intrahepatic Cholestasis Type 3 | Aplastic Anemia | Hidradenitis | Leukoencephalopathy, Progressive Multifocal | Thalassemia, Beta | Ophthalmoplegia | Spinal And Bulbar Muscular Atrophy | Impulse Control Disorder | Pemphigus Foliaceus | Scoliosis | Spitz Nevus | Generalized Epilepsy And Paroxysmal Dyskinesia | Rubeosis Iridis | Antithrombin III Deficiency | Autosomal Recessive Spastic Paraplegia Type 54 | Mucolipidosis Type III | Spondyloperipheral Dysplasia | Mesothelioma, Malignant | Congenital Disorders Of Glycosylation Type II | Hyperlipidemia, Familial Combined | Hemophagocytic Lymphohistiocytosis | Fanconi Anemia | Metanephric Adenoma | Tic Disorder | Cancer, Brain | 3-methylglutaconic Aciduria Type I | Angioedema, Acquired | Charcot-Marie-Tooth Disease Axonal Type 2N | Cancer, Kidney | Fuchs Dystrophy | Lymphedema-distichiasis Syndrome | Pontocerebellar Hypoplasia Type 7 | Charcot-Marie-Tooth Disease Type 4E | Leukodystrophies | Hypoparathyroidism | Ovarian Sex Cord-stromal Tumor | Brenner Tumor | Hemangioendothelioma | Erythrokeratodermia Variabilis | Spinal Muscular Atrophy Type 3 | Mohr-Tranebjaerg Syndrome | Restrictive Dermopathy | Acromegaly | Agranulocytosis | Proximal Symphalangism | Spina Bifida | Cantu Syndrome | Carbamoyl Phosphate Synthetase I Deficiency | Hyperthermia, Malignant | Microcephaly, Seizures, And Developmental Delay | Epidermolytic Hyperkeratosis | Cardiomyopathy, Peripartum | Diastrophic Dysplasia | Charcot-Marie-Tooth Disease, Type 1A | Cerebrotendinous Xanthomatosis | Choroideremia | Macrophagic Myofasciitis | Pulmonary Capillary Hemangiomatosis | Eccrine Porocarcinoma | Neurofibromatosis Type 1 | Calcium Pyrophosphate Deposition Disease | Immunoproliferative Disorders | Charcot-Marie-Tooth Disease Type 2T | Arteriovenous Malformations | Schistosomiasis Mansoni | Parkinsonism | Erectile Dysfunction | Acrodermatitis | Wagner Disease | Primary Hyperoxaluria Type 1 | Guttate Psoriasis | Meier-Gorlin Syndrome | Tinea | Xeroderma Pigmentosum | Auriculocondylar Syndrome | Conduct Disorder | Thymoma, Malignant | Colitis, Lymphocytic | Myelofibrosis | Congenital Heart Block | Schaaf-Yang Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Neurocutaneous Melanocytosis | Infantile Neuroaxonal Dystrophy | Xeroderma Pigmentosum Variant Type | Multiple Myeloma | Neurodermatitis | Schindler Disease | Turner's Syndrome | Hepatorenal Syndrome | Hyperinsulinemia | Diabetes | Adenocarcinoma | 3-methylglutaconic Aciduria Type IV | Pulmonary Sclerosing Hemangioma | Norrie Disease | Primary Erythromelalgia | Amenorrhea | Beare-Stevenson Syndrome | Woodhouse-Sakati Syndrome | Diabetes Type 1 | Cholestasis | Duane Retraction Syndrome | Oculodentodigital Dysplasia | NGLY1 Deficiency | Maple Syrup Urine Disease | Trigonocephaly | Primary Torsion Dystonia | Lipid Storage Diseases | Gyrate Atrophy Of The Choroid And Retina | Stuve-Wiedemann Syndrome | Familial Dysautonomia | Hypertension, Essential | Primrose Syndrome | Fibrodysplasia Ossificans Progressiva | Congenital Tufting Enteropathy | B-cell Prolymphocytic Leukemia | Peeling Skin Syndrome, Acral Type | Anodontia | Aceruloplasminemia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Eosinophilia | Dyslipidemia | Castleman Disease | Epidermolysis Bullosa | Schnyder Crystalline Corneal Dystrophy | Torticollis | Pseudohypoparathyroidism Type 1C | Chromosome 9q34.3 Deletion Syndrome | Chediak-Higashi Syndrome | Sarcoidosis | Thyroid Dysgenesis | Iron Metabolism Disorders | Postpoliomyelitis Syndrome | LRBA Deficiency | Wolfram Syndrome | Leukocyte Adhesion Deficiency | Hypogonadism | Hypercalcemia | Noonan Syndrome-like Disorder With Loose Anagen Hair | Central Retinal Artery Occlusion | Learning Disability | Alcoholism | Nevus | Tyrosinemia Type 1 | Sialoadenitis | Currarino Syndrome | Idiopathic Pulmonary Fibrosis | Renal Hypomagnesemia 3 | Ornithine Transcarbamylase Deficiency | Familial Retinal Arterial Macroaneurysm | Familial Pheochromocytoma-paraganglioma | Chromosome 5q Deletion Syndrome | Spinocerebellar Ataxia Type 42 | Mitochondrial Encephalomyopathy | Chronic Myelomonocytic Leukemia | Chronic Inflammatory Demyelinating Polyneuropathy | Anorectal Malformations | Seizures-scoliosis-macrocephaly Syndrome | Retinitis Pigmentosa | Neurofibroma | Parvovirus B19 Infection | Leukemia | Isobutyryl-CoA Dehydrogenase Deficiency | Rhabdomyosarcoma | Neurofibroma, Plexiform | Osteogenesis Imperfecta Type I | Chronic Granulomatous Disease | Rosacea | Juvenile Myoclonic Epilepsy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Huntington's Disease-like 2 | Systemic Lupus Erythematosus | Smith-Kingsmore Syndrome | Astrocytoma, Anaplastic | Exotropia | Carcinoma, Small Cell | Motion Sickness | REM Sleep Behavior Disorder | Agnathia-Otocephaly Complex | Osteochondrosis | Myofibrillar Myopathy | Anti-glomerular Basement Membrane Disease | Thyroid Dyshormonogenesis | Pseudohypoaldosteronism | Carpenter Syndrome | Renal Tubular Acidosis | Choriocarcinoma | Hypoplastic Left Heart Syndrome | Angioimmunoblastic T-cell Lymphoma | Stargardt Disease | Renal Failure | Neuromyotonia | Alpha-1 Antitrypsin Deficiency | Mitochondrial Disease | Lung Diseases | Chromosome 16p11.2 Deletion Syndrome | Oligodendroglioma | Charcot-Marie-Tooth Disease, Type 2 | Congenital Fiber-type Disproportion Myopathy | Neuroectodermal Tumors, Primitive | Limb Girdle Muscular Dystrophy | DRESS Syndrome | Acute Tubular Necrosis | Kernicterus | Bronchiolitis | Congenital Adrenal Hyperplasia 1 | Richter's Syndrome | GM2-gangliosidosis AB Variant | Periodontitis | Myeloid Leukemia | Chitayat Syndrome | Rhinitis | Axenfeld-Rieger Syndrome | Acute Coronary Syndrome | Porencephaly | Hypertensive Nephropathy | Swine Influenza | PASLI Disease | Primary Carnitine Deficiency | Mannosidase Deficiency Diseases | Muscle Wasting | Vitamin B12 Deficiency | Progressive External Ophthalmoplegia | Pontocerebellar Hypoplasia Type 2 | Tuberculous Meningitis | Opisthorchiasis | Toxic Epidermal Necrolysis | Epithelial-myoepithelial Carcinoma | Hamartoma | Delayed Sleep Phase Syndrome | Esophageal Motility Disorders | Epidermolytic Ichthyosis, Annular | Hypervalinemia | Adrenoleukodystrophy, X-linked | Combined Deficiency Of Factor V And Factor VIII | 3-methylcrotonyl-CoA Carboxylase Deficiency | Varicocele | Astigmatism | Carcinoid Syndrome | Chronic Thromboembolic Pulmonary Hypertension | Glioblastoma Multiforme | Hidradenitis Suppurativa | Hemorrhoids | Atopic Dermatitis | Premature Ejaculation | Myhre Syndrome | Malignant Fibrous Histiocytoma | Ophthalmia, Sympathetic | Iron Overload | Uremia | Macular Corneal Dystrophy | Diabetes Type 2 | Acute Lymphocytic Leukemia | Spinocerebellar Ataxia Type 14 | Chronic Granulomatous Disease, X-linked | Marinesco-Sjogren Syndrome | Galactosialidosis | Ghosal Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Wiskott-Aldrich Syndrome | Brooke-Spiegler Syndrome | Pulmonary Alveolar Proteinosis | Congenital Dysfibrinogenemia | X-linked Creatine Transporter Deficiency | Cardiospondylocarpofacial Syndrome | Neuroleptic Malignant Syndrome | Proteasome-associated Autoinflammatory Syndrome 2 | Nephronophthisis | Neurofibromatosis-Noonan Syndrome | Fibrillation, Atrial | Trachoma | Skin Fragility-woolly Hair Syndrome | Non-Hodgkin Lymphoma | Fundus Albipunctatus | Acquired Partial Lipodystrophy | Keratocystic Odontogenic Tumor | Van Der Knaap Disease | Alazami Syndrome | Keratoconjunctivitis | Acrodermatitis Enteropathica | Glutaric Aciduria Type 1 | Pituitary Dwarfism | Precocious Puberty | MIRAGE Syndrome | Hemochromatosis Type 2 | Pneumonia, Mycoplasma | Microphthalmia, Syndromic 7 | Waardenburg Syndrome | Rothmund-Thomson Syndrome | Cold-induced Sweating Syndrome | Tetanus | Otitis Media | Whipple's Disease | Spinocerebellar Ataxia Type 21 | Carcinoid Tumor | Hypercholesterolemia, Familial | Polycythemia Vera | Spondylometaphyseal Dysplasia | Spinocerebellar Ataxia Type 10 | Best Macular Dystrophy | Cocaine-Related Disorders | Osmotic Demyelination Syndrome | Muir-Torre Syndrome | Diamond-Blackfan Anemia | Anemia | Sclerosing Cholangitis | Arthrogryposis | Scapuloperoneal Spinal Muscular Atrophy | Congenital Primary Aphakia | Multiple Sclerosis, Relapsing-remitting | Infectious Diarrhea | Hypopituitarism | Pericarditis | Glioblastoma | Liver Diseases | Basan Syndrome | Blepharophimosis Syndrome | Okihiro Syndrome | Myelitis, Transverse | Congenital Ichthyosiform Erythroderma | Silver-Russell Syndrome | Milk Allergy | Trichomegaly | Pneumothorax | Sarcoma, Ewing | Addison Disease | Sickle Cell Anemia | Necrobiosis Lipoidica | Kindler Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Pemphigus Vulgaris | Liver Failure | Ataxia-ocular Apraxia 2 | Pulverulent Zonular Cataract | Alveolar Capillary Dysplasia | Melanocytic Nevus | Spinal Cord Diseases | L-2-Hydroxyglutaric Aciduria | Hypobetalipoproteinemias | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Netherton Syndrome | Lipodystrophy | Pyloric Stenosis, Infantile Hypertrophic | Portal Vein Thrombosis | Primary Familial Brain Calcification | Benign Familial Infantile Seizures | Coma | Fowler's Syndrome | Infertility, Male | Microphthalmia | Trichorhinophalangeal Syndrome | Lattice Corneal Dystrophy Type 1 | Alkaptonuria | CREST Syndrome | Vici Syndrome | C3 Glomerulopathy | Walker-Warburg Syndrome | Galloway-Mowat Syndrome | Split Hand-foot Malformation | Ebstein Anomaly | X-linked Myotubular Myopathy | Peters-plus Syndrome | Bronchitis, Chronic | Cancer, Skin | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Paroxysmal Nocturnal Hemoglobinuria | Canavan Disease | Chudley-McCullough Syndrome | Chylomicron Retention Disease | GLUT1 Deficiency Syndrome | Gynecomastia | Anorchia | Long QT Syndrome Type 3 | Babesiosis | Chorea | Hyperhomocysteinemia | Prolidase Deficiency | Aphasia | Early Infantile Epileptic Encephalopathy 1 | Eiken Syndrome | Desmosterolosis | Granular Corneal Dystrophy Type 1 | Carney-Stratakis Syndrome | Becker Muscular Dystrophy | Creutzfeldt-Jakob Disease | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Spinocerebellar Ataxia Type 20