Asperger Syndrome

About the Disease
Asperger Syndrome, also known as asperger syndrome, susceptibility to, is related to autism spectrum disorder and autism. An important gene associated with Asperger Syndrome is ASPG2 (Asperger Syndrome, Susceptibility To, 2), and among its related pathways/superpathways are Transmission across Chemical Synapses and Neurogenesis regulation in the olfactory epithelium. The drugs Risperidone and Milnacipran have been mentioned in the context of this disorder. Affiliated tissues include brain, amygdala and caudate nucleus, and related phenotypes are nervous system and normal

Common Targets
MGLL | NHS | ARNT2 | OXT | CSMD1 | UPF3B | FRMPD4 | DOCK4 | OGT | LINC01830 | FSTL4 | OXTR | LOC730100 | ARMC2 | HCFC1 | ZNF182 | COMT | DIPK2B

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

Other Diseases

Anorectal Malformations | Lipodystrophy | Juvenile Polyposis | Adult Polyglucosan Body Disease | Spinocerebellar Ataxia Type 7 | Waardenburg Syndrome Type 4A | Treacher Collins Syndrome | Scleroderma | Adrenoleukodystrophy, X-linked | Fibrodysplasia Ossificans Progressiva | Urofacial Syndrome | Acute Lymphocytic Leukemia | Meckel-Gruber Syndrome | Biotinidase Deficiency | Sialidosis | Autosomal Recessive Bestrophinopathy | Spinal And Bulbar Muscular Atrophy | Lennox-Gastaut Syndrome | Atrial Septal Defect | Alpers Syndrome | Charcot-Marie-Tooth Disease | Esophageal Adenocarcinoma | Leukemia | GM2-gangliosidosis AB Variant | Rett Syndrome | Arthropathy | Cystitis | Acute Lung Injury | Clouston Hidrotic Ectodermal Dysplasia | Noonan Syndrome-like Disorder With Loose Anagen Hair | Periodic Limb Movement Disorder | Hereditary Multiple Exostoses | Keratosis, Actinic | Hypersomnia | Keratoconus | Androgenic Alopecia | Sarcoma | Zygomycosis | Nephrosclerosis | Monilethrix | Hypertelorism | Trichuriasis | Methemoglobinemia | Mitochondrial DNA Depletion Syndrome | Oligoastrocytoma | Smoldering Myeloma | Gitelman Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Asperger Syndrome | Lipid Storage Diseases | Leprosy | Dysmorphophobia | Ameloblastoma | Aspartylglycosaminuria | 3-methylglutaconic Aciduria | Adrenomyeloneuropathy | Hyperkeratosis | Dyggve-Melchior-Clausen Disease | Placenta Previa | Thyroid Dysgenesis | Blood Protein Disorders | Dwarfism | Pilomatrix Carcinoma | Chondrodysplasia Punctata 1, X-linked Recessive | Localized Scleroderma | Rickets | Facioscapulohumeral Muscular Dystrophy | Reflex Epilepsy | Spinocerebellar Ataxia Type 10 | Myotonic Disorders | Neurodermatitis | Hodgkin Lymphoma | Neovascular Glaucoma | Kallmann Syndrome | Encephalocele | Rosacea | Frontometaphyseal Dysplasia | Chronic Leukemia | Gastritis | Atrioventricular Septal Defect | Speech Disorders | WAGR Syndrome | Congenital Fiber-type Disproportion Myopathy | Hypertension, Portal | Autosomal Recessive Spastic Paraplegia Type 54 | Prader-Willi Syndrome | Vestibular Disease | Vitamin A Deficiency | Beta-Propeller Protein-associated Neurodegeneration | Periodontitis | Bronchitis | Lymphoma | Exotropia | Tietze Syndrome | Schizoaffective Disorder | Chronic Beryllium Disease | Pyruvate Dehydrogenase Deficiency | Angiosarcoma Of The Breast | Dermatitis | Tibial Muscular Dystrophy | Insulin Resistance | Costello Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Duodenal Atresia | Hepatitis | Citrullinemia | Chronic Periodontitis | DEND Syndrome | Glaucoma | Steel Syndrome | Macrophage Activation Syndrome | Cystinosis | Molybdenum Cofactor Deficiency | Keratitis-ichthyosis-deafness Syndrome | Muscular Dystrophy | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | McLeod Syndrome | Twin-to-twin Transfusion Syndrome | Cyclic Vomiting Syndrome | Presbycusis | Rotor Syndrome | Neuromuscular Disorders | Vitreoretinal Degeneration, Snowflake Type | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Pernicious Anemia | Aphasia | Sickle Cell Anemia | Schamberg Disease | Epithelial-myoepithelial Carcinoma | Keratoacanthoma | Dysequilibrium Syndrome | Scapuloperoneal Spinal Muscular Atrophy | Megaloblastic Anemia | Rhabdomyosarcoma, Embryonal | Pneumonia, Viral | Polyradiculopathy | Otitis Media | Familial Mediterranean Fever | Chudley-McCullough Syndrome | Atopic Dermatitis | Primary Familial Brain Calcification | Aromatic L-amino Acid Decarboxylase Deficiency | Congenital Generalized Lipodystrophy | Carotid Artery Disease | Protein S Deficiency | Seasonal Mood Disorder | Adrenal Insufficiency | Leigh Syndrome | Hemoglobinopathies | Esophagitis | Kindler Syndrome | Hereditary Spastic Paraplegia | Acne Vulgaris | Cataract | Congenital Absence Of Vas Deferens | Metabolic Syndrome | Polyneuropathy | Cramp Fasciculation Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Blepharophimosis Syndrome | Nephrotic Syndrome Type 1 | Cervical Dystonia | Ganglioglioma | Cutis Laxa | Filariasis | Neurofibromatosis | Raine Syndrome | Optic Neuritis | Shprintzen-Goldberg Syndrome | Behavioral Variant Of Frontotemporal Dementia | Cerebellofaciodental Syndrome | Hemolytic Uremic Syndrome | Hemimegalencephaly | Metachondromatosis | B-cell Prolymphocytic Leukemia | Alpha-thalassemia Myelodysplasia Syndrome | Chondrodysplasia Punctata | Congenital Central Hypoventilation Syndrome | Sensory Neuropathy | Generalized Epilepsy And Paroxysmal Dyskinesia | Neurofibroma | Ocular Hypertension | Hyperinsulinemia | Hemangioma | Compartment Syndrome | Hypertension, Renovascular | Lymphangioleiomyomatosis | Prolactinoma | Succinic Semialdehyde Dehydrogenase Deficiency | Apparent Mineralocorticoid Excess Syndrome | Rhabdomyosarcoma | Diffuse Intrinsic Pontine Glioma | Pompe Disease | Leri Pleonosteosis | Craniometaphyseal Dysplasia | Sarcoma, Endometrial Stromal | Spinocerebellar Ataxia Type 5 | REM Sleep Behavior Disorder | Spondyloperipheral Dysplasia | Obsessive-compulsive Disorder | Hereditary Inclusion Body Myopathy | Cold Agglutinin Disease | Myoclonic Atonic Epilepsy | Lipid Metabolism Disorders | Behcet's Disease | Sleep Apnea, Central | Niemann-Pick Disease, Type B | Angiodysplasia | Axenfeld-Rieger Syndrome | Senior-Loken Syndrome | Familial Partial Lipodystrophy | Osteogenesis Imperfecta Type II | Insulinoma | Progressive Osseous Heteroplasia | Pulverulent Zonular Cataract | Porphyria, Acute Intermittent | Hyperferritinemia-cataract Syndrome | Osteoglophonic Dysplasia | Danon Disease | Thrombotic Microangiopathy | Neuronal Ceroid Lipofuscinosis | Amish Infantile Epilepsy Syndrome | Leukoplakia | Leiomyoma | Microphthalmia | Spinocerebellar Ataxia Type 13 | Coloboma | Glutaric Aciduria Type 3 | Triple A Syndrome | McCune-Albright Syndrome | Granuloma Annulare | Proteasome-associated Autoinflammatory Syndrome 2 | Shwachman-Bodian-Diamond Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Sporadic Inclusion Body Myositis | Hyperostosis | Kearns-Sayre Syndrome | Wolman Disease | Diabetic Neuropathy | Fragile X Syndrome | Iron Metabolism Disorders | Hyperuricemic Nephropathy, Familial Juvenile | Bronchiectasis | Charcot-Marie-Tooth Disease, Type 2C | Tinea | Tyrosinemia Type 1 | Gastroschisis | Hemosiderosis | X-linked Myotubular Myopathy | Hypopigmentation | Wolff-Parkinson-White Syndrome | Trichorhinophalangeal Syndrome | Pneumonia, Mycoplasma | HUPRA Syndrome | Multiple Myeloma | Thrombocythemia, Essential | Ichthyosis Bullosa Of Siemens | Tangier Disease | Myhre Syndrome | Chiari Malformation Type I | Hermansky-Pudlak Syndrome | Chloridorrhea, Congenital | Hypotension, Orthostatic | Asthma, Exercise-induced | Constipation | Pityriasis Rubra Pilaris | Sarcomatoid Carcinoma Of The Lung | Dominant Optic Atrophy | Non-Langerhans Cell Histiocytosis | Megalencephaly | Transient Bullous Dermolysis Of The Newborn | TARP Syndrome | Stromal Corneal Dystrophy | Ectodermal Dysplasia | Fibrosarcoma | Greig Cephalopolysyndactyly Syndrome | Osteosclerosis | Marinesco-Sjogren Syndrome | Bacterial Meningitis | Wolcott-Rallison Syndrome | Leukemia-lymphoma, Adult T-cell | Cornelia De Lange Syndrome | Angelman Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Globozoospermia | Hypertension, Renal | Pontocerebellar Hypoplasia | Lymphedema | Leukodystrophies | Fibrosis | Brenner Tumor | Hydrocephalus, Normal Pressure | Hyperparathyroidism, Primary | Basal Ganglia Disease, Biotin-responsive | Neurofibromatosis-Noonan Syndrome | Genee-Wiedemann Syndrome | Mixed Connective Tissue Disease | Congenital Dyserythropoietic Anemia Type 4 | Keratoconjunctivitis | Acute Anterior Uveitis | Scleritis | Polycystic Ovary Syndrome | Craniolenticulosutural Dysplasia | Spermatocele | Epidermolysis Bullosa Dystrophica | HIBCH Deficiency | Dengue Hemorrhagic Fever | Skin Papilloma | Hereditary Spherocytosis | Epidermolysis Bullosa Simplex, Localized | Rash | Centronuclear Myopathy | Mumps | Infantile Neuroaxonal Dystrophy | Erythrokeratodermia Variabilis | Subacute Sclerosing Panencephalitis | Nail-Patella Syndrome | Demyelinating Diseases | Amyotrophic Lateral Sclerosis | Fanconi Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | Hepatitis B, Chronic | Vitelliform Macular Dystrophy | Familial Hypertrophic Cardiomyopathy | Neuroendocrine Cancer | Dyslexia | Infertility, Male | Warsaw Breakage Syndrome | Osteoporosis-pseudoglioma Syndrome | Encephalopathy, Glycine | Frank-ter Haar Syndrome | Aldosterone Deficiency | Alveolar Capillary Dysplasia | Facioscapulohumeral Muscular Dystrophy Type 1 | Intermittent Explosive Disorder | Subcortical Band Heterotopia | Dermatitis Herpetiformis | Diastrophic Dysplasia | Charcot-Marie-Tooth Disease Type 2D | Erdheim-Chester Disease | Hydronephrosis | Colitis, Collagenous | Spinocerebellar Ataxia Type 3 | Kashin-Beck Disease | Asplenia | Persistent Hyperplastic Primary Vitreous | Common Cold | Triphalangeal Thumb-polysyndactyly Syndrome | Stickler Syndrome | Emery-Dreifuss Muscular Dystrophy | Feingold Syndrome | Aldosteronism | Bardet-Biedl Syndrome | Osteopathia Striata With Cranial Sclerosis | Alpha-1 Antitrypsin Deficiency | Hypoparathyroidism | Varicocele | Fanconi Anemia | Chromosome 5q Deletion Syndrome | Macrophagic Myofasciitis | Occipital Neuralgia | Carcinoma, Squamous Cell | Hypertension | Desbuquois Syndrome | Infectious Diarrhea | Glycogen Storage Disease Type 9 | Hemochromatosis Type 1 | Hyperkalemic Periodic Paralysis | Focal Cortical Dysplasia Type 2 | Basal Ganglia Cerebrovascular Disease | GLUT1 Deficiency Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Peeling Skin Syndrome Type B | Aarskog-Scott Syndrome | Carbohydrate Metabolism Disorders | Polymyositis | Immunoproliferative Disorders | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Carney Triad | Bronchitis, Chronic | Niemann-Pick Disease, Type C | Adenosine Deaminase 2 Deficiency | Congenital Bile Acid Synthesis Defect | Obesity | Paget's Disease Of The Breast | Hyperekplexia | Gastrointestinal Disorders | Hereditary Neuropathy With Liability To Pressure Palsies | Impulse Control Disorder | Saul-Wilson Syndrome | Acute Tubular Necrosis | Influenza | Superficial Spreading Melanoma | Takenouchi-Kosaki Syndrome | Allergic Contact Dermatitis | Glycogen Storage Disease | Spinocerebellar Ataxia Type 40 | Cutaneous Lupus Erythematosus | Mucolipidosis Type III | H Syndrome