Dysmorphophobia

About the Disease
Body Dysmorphic Disorder, also known as dysmorphophobia, is related to social phobia and bulimia nervosa. An important gene associated with Body Dysmorphic Disorder is DLGAP3 (DLG Associated Protein 3), and among its related pathways/superpathways is "Selective Serotonin Reuptake Inhibitor Pathway, Pharmacodynamics". The drugs Levetiracetam and Venlafaxine have been mentioned in the context of this disorder. Affiliated tissues include brain, breast and colon.

Common Targets
CACNA1B | SV2A

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

Other Diseases

X-linked Myotubular Myopathy | Dystrophy, Cone-rod | Anal Fissure | VACTERL Association | Angioedema | Lymphoma Lymphoblastic | Hernia, Inguinal | Ophthalmia, Sympathetic | Hypertension, Renovascular | Hereditary Xerocytosis | Heterotopic Ossification | Cystitis, Interstitial | Choroideremia | Lymphoma, AIDS-related | Nephronophthisis | Kleine-Levin Syndrome | Allergic Contact Dermatitis | Cousin Syndrome | Platelet Disorders | Chorea-acanthocytosis | Hypersensitivity | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Acanthosis Nigricans | Peeling Skin Syndrome, Acral Type | Ulcerative Colitis | Rhinitis | Premature Ejaculation | Sertoli Cell-only Syndrome | Thyroid Dysgenesis | Thin Basement Membrane Disease | Heimler Syndrome | LMNA-related Congenital Muscular Dystrophy | Analgesia | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Sick Sinus Syndrome | Nestor-Guillermo Progeria Syndrome | Bicuspid Aortic Valve | Spitzoid Melanoma | Rubinstein-Taybi Syndrome | Absence Epilepsy | Otitis Media | Lymphopenia | Benign Familial Pemphigus | Carpenter Syndrome | Spinal Muscular Atrophy Type 2 | Osteoporosis | Motion Sickness | Chronic Thromboembolic Pulmonary Hypertension | Pre-eclampsia | Fanconi Syndrome | Renal Tubular Dysgenesis | Asthma, Nocturnal | CEDNIK Syndrome | Chondroma | Spinocerebellar Ataxia Type 27 | VEXAS Syndrome | Coenzyme Q10 Deficiency | Wagner Disease | Mesothelioma, Malignant | Saul-Wilson Syndrome | Intracranial Hypertension | Progressive Myoclonic Epilepsy | Sulfite Oxidase Deficiency | Pupil Disorders | Retinopathy, Diabetic | Pantothenate Kinase-associated Neurodegeneration | Pierson Syndrome | Hemoglobinopathies | Pulmonary Tuberculosis | Optic Neuropathy, Anterior Ischemic | Congenital Tufting Enteropathy | Glaucoma | Tibial Muscular Dystrophy | Esophageal Motility Disorders | Familial Exudative Vitreoretinopathy | Pineoblastoma | Spinocerebellar Ataxia Type 7 | Burn-McKeown Syndrome | Acute Myeloid Leukemia | Cardiomyopathy, Restrictive | Hyperoxaluria | Wolfram Syndrome | Leri Pleonosteosis | Nephroblastoma | Monilethrix | Pseudoexfoliation Syndrome | Pulverulent Zonular Cataract | Blepharo-cheilo-odontic Syndrome | Retinal Telangiectasia | Waardenburg Syndrome Type 2A | Charcot-Marie-Tooth Disease Type 2T | Plasmacytoma | Dubin-Johnson Syndrome | Nutrition Disorders | Congenital Dyserythropoietic Anemia | Optic Neuritis | Myocardial Infarction | Disseminated Superficial Actinic Porokeratosis | Central Core Disease | Lymphoproliferative Disorders | Stroke, Ischemic | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Riboflavin Transporter Deficiency Neuronopathy | Glutaric Aciduria Type 1 | Arthritis, Psoriatic | Non-Langerhans Cell Histiocytosis | Spinocerebellar Ataxia Type 40 | Triphalangeal Thumb-polysyndactyly Syndrome | Lymphoproliferative Disease, X-linked | Chromosome 5q Deletion Syndrome | Postaxial Polydactyly | Periodontitis | Impetigo | Treacher Collins Syndrome | Panniculitis | Myopia | Major Depression | Seizures | Ichthyosis | Congenital Central Hypoventilation Syndrome | Yellow Fever | Glutaric Aciduria Type 3 | Hereditary Pyropoikilocytosis | Robinow Syndrome | Vulvovaginitis | Scapuloperoneal Spinal Muscular Atrophy | Avian Influenza | Progressive Familial Intrahepatic Cholestasis Type 3 | Infantile Refsum Disease | Periodic Limb Movement Disorder | Lipodystrophy | Myhre Syndrome | Muscle Wasting | KBG Syndrome | Borderline Personality Disorder | Esophagitis | Metachondromatosis | Encephalopathy, Hepatic | Thrombophilia | Endometrial Hyperplasia | Spinocerebellar Ataxia Type 31 | Retinitis Pigmentosa 3 | Asthma | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Kallmann Syndrome | Melanocytic Nevus | Centronuclear Myopathy | Kawasaki Disease | Mitochondrial DNA Depletion Syndrome 13 | Gingivitis | Sclerosing Cholangitis | Pseudohypoparathyroidism Type 1B | Filariasis | Prostatitis | Dysthymia | Mountain Sickness | Familial Digital Arthropathy-brachydactyly | Hyperbilirubinemia | Optic Nerve Diseases | Acute Leukemia | REM Sleep Behavior Disorder | Esthesioneuroblastoma | Antisocial Personality Disorder | Prolactinoma | Thrombotic Microangiopathy | TARP Syndrome | Hyperparathyroidism | Autosomal Recessive Congenital Ichthyosis | Psoriasis | Congenital Adrenal Hyperplasia 1 | Angioedema, Hereditary | Neurofibromatosis | Acral Lentiginous Melanoma | Anti-NMDA Receptor Encephalitis | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Asperger Syndrome | Vitamin D Deficiency | Osteogenesis Imperfecta Type I | Ameloblastic Carcinoma | Schistosomiasis | Common Variable Immunodeficiency | Gastrointestinal Disorders | Meconium Ileus | Diabetes | Myotonia | Desmosterolosis | Constipation | Cholangiocarcinoma | Wolcott-Rallison Syndrome | Carcinoid Syndrome | Agoraphobia | Anxiety Disorders | Carpal Tunnel Syndrome | Familial Retinal Arterial Macroaneurysm | Hyperprolactinemia | Lesch-Nyhan Syndrome | Vestibular Disease | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Lysosomal Acid Lipase Deficiency | Renal Failure | Osteonecrosis Of The Jaw | Glaucoma, Congenital | Skin Fragility-woolly Hair Syndrome | Paraganglioma, Carotid Body | Fibrosis | Muscular Dystrophy | Ocular Surface Squamous Neoplasia | Cardiac Sarcoidosis | Kaposiform Hemangioendothelioma | POEMS Syndrome | Hypophosphatasia | Kashin-Beck Disease | Glaucomatocyclitic Crisis | Conjunctivitis | Progressive Familial Intrahepatic Cholestasis | Spina Bifida | Optic Nerve Hypoplasia, Bilateral | Spinocerebellar Ataxia Type 8 | Tylosis With Esophageal Cancer | Obesity | Intermittent Claudication | Leiomyosarcoma | Pigment Dispersion Syndrome | Liver Diseases | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Osteochondrosis | Glucagonoma | Intestinal Pseudo-obstruction | Coronary Heart Disease | Triple A Syndrome | Bare Lymphocyte Syndrome | Nephrotic Syndrome Type 1 | Dermatitis Herpetiformis | Meckel-Gruber Syndrome | Netherton Syndrome | Nephrosclerosis | Dermatomyositis | Megaloblastic Anemia | Rhabdoid Tumor | Hypersensitivity Pneumonitis | Hypercalcemia | Lymphangioma | Hypertensive Retinopathy | Glycogen Storage Disease Type 1 | Dermatofibrosarcoma | Pontocerebellar Hypoplasia Type 2 | Paraganglioma | Hyperinsulinemic Hypoglycemia | Sialoadenitis | Hereditary Sensory And Autonomic Neuropathy | Cirrhosis | Porphyria, Acute Intermittent | Colon Adenoma | Myoclonus-dystonia Syndrome | Ebstein Anomaly | Niemann-Pick Disease, Type C | Hemangioblastoma | Mastitis | Keratocystic Odontogenic Tumor | Lichen Sclerosus | Parapsoriasis | Ocular Hypertension | Rhizomelic Chondrodysplasia Punctata | Xeroderma Pigmentosum Variant Type | 3C Syndrome | Sclerocornea | Hypocalcemia | Otosclerosis | Hypopituitarism | Medulloblastoma | Hereditary Neuropathy With Liability To Pressure Palsies | Hydrocephalus | Conjunctivitis, Allergic | Schwartz-Jampel-Aberfeld Syndrome | Glioblastoma Multiforme | Ectrodactyly | Tic Disorder | Brugada Syndrome 1 | Hepatitis C, Chronic | Encephalitis | Porphyria, Variegate | Spinal Cord Diseases | Disseminated Intravascular Coagulation | Colitis | Neuroma | Mitochondrial Encephalomyopathy | Hepatitis E | Greenberg Dysplasia | Demyelinating Diseases | Usher Syndrome Type I | Trimethylaminuria | Costello Syndrome | Herpes Genitalis | Primary Progressive Aphasia | Diamond-Blackfan Anemia | Familial Hypertrophic Cardiomyopathy | Metanephric Adenoma | 3-methylglutaconic Aciduria | Carbamoyl Phosphate Synthetase I Deficiency | Gastroenteritis, Eosinophilic | High Molecular Weight Kininogen Deficiency | Multicentric Carpotarsal Osteolysis Syndrome | Crohn's Disease | Open-angle Glaucoma | Pseudohypoparathyroidism Type 1C | Familial Mediterranean Fever | Idiopathic Multicentric Castleman Disease | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Anorectal Malformations | GNE Myopathy | Microcephaly, Seizures, And Developmental Delay | Thromboembolism | Mucolipidosis | Paroxysmal Nocturnal Hemoglobinuria | Primary Carnitine Deficiency | Autism | Chromosome 17q21.31 Deletion Syndrome | Diarrhea | Impulse Control Disorder | Retinal Diseases | Metabolic Diseases | Perry Syndrome | Pneumothorax | Nemaline Myopathy 10 | Benign Hereditary Chorea | Desbuquois Syndrome | Avellino Corneal Dystrophy | Language Disorders | Zellweger Syndrome | Fraser Syndrome | Hyperacusis | Aicardi-Goutieres Syndrome | Eiken Syndrome | Alzheimer Disease, Late Onset | Carcinoma, Merkel Cell | Sickle Cell Anemia | Obesity, Morbid | Blepharitis | Loeys-Dietz Syndrome Type 4 | Spinocerebellar Ataxia Type 23 | Periventricular Nodular Heterotopia | Spondyloarthritis | Alkaptonuria | Blepharospasm | Evans Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Encephalitis, Tick-borne | Bietti Crystalline Dystrophy | Noonan Syndrome-like Disorder With Loose Anagen Hair | Otitis Externa | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Long QT Syndrome Type 1 | Porencephaly | Argininosuccinic Aciduria | Lung Diseases | Periventricular Leukomalacia | DOCK8 Immunodeficiency Syndrome | Von Hippel-Lindau Disease | LEOPARD Syndrome | Stroke, Hemorrhagic | Hemimegalencephaly | Peritonitis | Carcinoma, Small Cell | Uveitis, Anterior | Sarcoma, Alveolar Soft Part | Osteoarthritis | Erectile Dysfunction | Colitis, Collagenous | Panuveitis | Episodic Ataxia Type 1 | Pyruvate Dehydrogenase Deficiency | Fetal And Neonatal Alloimmune Thrombocytopenia | Familial Cerebral Amyloid Angiopathy | Bronchiectasis | Phenylketonuria II | Leishmaniasis, Cutaneous | CREST Syndrome | Headache | Beckwith-Wiedemann Syndrome | Eczema | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Endophthalmitis | Congenital Nystagmus | Glutaric Aciduria Type 2 | Rothmund-Thomson Syndrome | Familial Hyperaldosteronism | Keratopathy | Bethlem Myopathy | Graft-versus-host Disease | Spasticity | Necrobiosis Lipoidica | Adenomyosis | Corneal Edema | Whipple's Disease | Diabetes Insipidus, Nephrogenic | Schuurs-Hoeijmakers Syndrome | Vertigo | Phosphoglycerate Dehydrogenase Deficiency | Waardenburg Syndrome Type 2 | Tietze Syndrome