Disease

Impulse Control Disorder

About the Disease
Impulse Control Disorder, also known as disruptive, impulse control, and conduct disorders, is related to pyromania and oppositional defiant disorder. An important gene associated with Impulse Control Disorder is DLGAP3 (DLG Associated Protein 3), and among its related pathways/superpathways are Class A/1 (Rhodopsin-like receptors) and Transmission across Chemical Synapses. The drugs Carbidopa and Levodopa have been mentioned in the context of this disorder. Affiliated tissues include brain, skin and liver, and related phenotypes are shRNA abundance <= 50% and nervous system

Common Targets
HTR2B | GPR52 | HTR2A | HCRTR1 | OPRD1 | TPH2 | DRD3 | SLC6A3 | OPRM1 | GRIN2B | GRM4 | DRD2 | OPRK1 | ADRA2C | COMT | DDC | HTR1A

疾病靶点研报
Impulse Control Disorder

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

Other Diseases

Asplenia | Sleep Disorder | Vitamin A Deficiency | Familial Episodic Pain Syndrome | Chronic Myeloid Leukemia | Persistent Hyperplastic Primary Vitreous | Knobloch Syndrome | Werner's Syndrome | Hidradenitis Suppurativa | Dermatitis Herpetiformis | Asthma | Guttate Psoriasis | Central Core Disease | Traboulsi Syndrome | Seborrheic Dermatitis | Meningioma, Benign | Progressive External Ophthalmoplegia | Early Infantile Epileptic Encephalopathy 1 | Anterior Segment Dysgenesis | Ectrodactyly | Iron Deficiency Anemia | Benign Familial Neonatal Convulsions | Infantile Spasm | Frank-ter Haar Syndrome | Chanarin-Dorfman Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Nasodigitoacoustic Syndrome | Hartsfield Syndrome | Osteogenesis Imperfecta Type I | Bronchiectasis | Hypoalbuminemia | Raine Syndrome | Arteriovenous Malformations | Rheumatoid Arthritis | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Thanatophoric Dysplasia Type 1 | Epiphyseal Chondrodysplasia, Miura Type | Atrial Septal Defect | Isovaleric Acidemia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Acute Chest Syndrome | Cantu Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Frontometaphyseal Dysplasia | Angiomyolipoma | Rhabdomyosarcoma, Alveolar | Cranial Nerve Disease | Mucolipidosis Type II | Cabezas Syndrome | Fibrosis | Purpura, Thrombotic Thrombocytopenic | Nemaline Myopathy 8 | Muscular Dystrophy | Neurodermatitis | Uremic Pruritus | Infantile Nephropathic Cystinosis | Arthritis, Gouty | Uremia | Infectious Diarrhea | Netherton Syndrome | Ureteropelvic Junction Obstruction | Blepharo-cheilo-odontic Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Hepatic Adenomatosis | Essential Fructosuria | Anencephaly | Dyslexia | Klinefelter Syndrome | Glaucomatocyclitic Crisis | Polycythemia Vera | Anorectal Fistula | Carcinoma In Situ | Muscle Wasting | Megalencephaly | Varices | Cryptorchidism | Encephalopathy | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Amyotrophic Lateral Sclerosis | Hemosiderosis | Urolithiasis | Hypohidrotic Ectodermal Dysplasia | Fahr Disease | Nephroblastoma | Macrophagic Myofasciitis | Pseudohypoaldosteronism | Schistosomiasis | Usher Syndrome | Frontotemporal Dementia | Spermatocele | Ulcerative Colitis | Cutaneous Mastocytosis | Anorexia Nervosa | Tracheal Disorders | Cole-Carpenter Syndrome | Craniolenticulosutural Dysplasia | Yellow Fever | Distal Spinal Muscular Atrophy | Hyper IgE Syndrome | Majeed Syndrome | Hereditary Coproporphyria | Chitayat Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Adenosine Deaminase 2 Deficiency | Paroxysmal Kinesigenic Dyskinesia | Lymphangioleiomyomatosis | Polycystic Kidney, Autosomal Recessive | Thrombotic Microangiopathy | Holoprosencephaly | Primary Sclerosing Cholangitis | Amebiasis | Hypoparathyroidism | Osteonecrosis | Hereditary Sensory Neuropathy Type 1 | Erdheim-Chester Disease | Cataplexy | Nephrotic Syndrome | Wieacker-Wolff Syndrome | Aromatic L-amino Acid Decarboxylase Deficiency | Polycythemia | Echinococcosis | Lipoma | Pseudohypoparathyroidism Type 2 | Pericarditis | Pulmonary Vein Stenosis | Sclerosing Cholangitis | Liver Failure | Progressive Osseous Heteroplasia | Erythema Nodosum | Steel Syndrome | Dyskeratosis Congenita | Batten Disease | Persistent Fetal Circulation | Spondylo-ocular Syndrome | Smith-Lemli-Opitz Syndrome | Dysgerminoma | Tetanus | Rotor Syndrome | Chondrodysplasia Punctata | Neurocysticercosis | CDKL5 Deficiency Disorder | Arthritis, Psoriatic | Hashimoto Thyroiditis | Hyperparathyroidism, Secondary | Presbycusis | Opisthorchiasis | Astrocytoma, Anaplastic | Pyruvate Dehydrogenase Deficiency | Cholelithiasis | Pure Red Cell Aplasia | Cocaine-Related Disorders | AIDS Dementia Complex | Blau Syndrome | Acrocallosal Syndrome | Ventricular Septal Defect | Apert Syndrome | Limb Girdle Muscular Dystrophy | Spondylocostal Dysostosis | Pontocerebellar Hypoplasia | Chiari Malformation Type I | Retinal Diseases | Papulopustular Rosacea | Orthostatic Intolerance | Ischemia | Osteopetrosis | Autonomic Neuropathy | Neurocutaneous Syndromes | Rubinstein-Taybi Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Von Willebrand Disease | Myoclonic Epilepsy With Ragged Red Fibers | Multiple Hamartoma Syndrome | Mast Cell Leukemia | Myoclonus | Pleurisy | KBG Syndrome | Vascular Cognitive Impairment | Takotsubo Cardiomyopathy | Mosaic Variegated Aneuploidy Syndrome 2 | Postpartum Depression | Hypopigmentation | Whipple's Disease | Spinocerebellar Ataxia Type 28 | Autoimmune Disease | Vitamin K Deficiency | Niemann-Pick Disease, Type A | Cannabis Abuse | Familial Retinal Arterial Macroaneurysm | Spinocerebellar Ataxia Type 12 | Bardet-Biedl Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Pachyonychia Congenita | Wolman Disease | Renal Tubular Acidosis | Smith-Kingsmore Syndrome | Hereditary Neuropathy With Liability To Pressure Palsies | Menetrier Disease | Systemic Mastocytosis | ADNP Syndrome | Pernicious Anemia | Erectile Dysfunction | Neuropathy | Tumoral Calcinosis | Gigantism | Isobutyryl-CoA Dehydrogenase Deficiency | Noonan Syndrome-like Disorder With Loose Anagen Hair | Basal Cell Nevus Syndrome | Pulmonary Alveolar Proteinosis | Necrobiosis Lipoidica | Hepatitis D | Hypotrichosis Simplex | Thrombophilia | Heimler Syndrome | Hypoproteinemia, Hypercatabolic | Spinocerebellar Ataxia Type 20 | Lafora Disease | Dermatofibrosarcoma | Schamberg Disease | Waldenstrom Macroglobulinemia | Fibromyalgia | Non-Langerhans Cell Histiocytosis | Leber Hereditary Optic Neuropathy | Diffuse Mesangial Sclerosis | Tangier Disease | Deafness, Dystonia, And Cerebral Hypomyelination | Venous Insufficiency | Congenital Disorders Of Glycosylation | Spasticity | Congenital Hemolytic Anemia | Thromboembolism | Antisocial Personality Disorder | Lymphomatoid Granulomatosis | Usher Syndrome Type I | Intracerebral Hemorrhage | Hypoplastic Left Heart Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Thanatophoric Dysplasia | Glycogen Storage Disease Type 1a | Dysequilibrium Syndrome | Tularemia | Renal Dysplasia | GNE Myopathy | Partington Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Focal Dermal Hypoplasia | Omenn Syndrome | Chudley-McCullough Syndrome | Double Outlet Right Ventricle | Discoid Lupus Erythematosus | Fucosidosis | Sleep Apnea, Obstructive | Diamond-Blackfan Anemia | Focal Facial Dermal Dysplasia | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | DEND Syndrome | Cousin Syndrome | Neonatal Progeroid Syndrome | Melanoma | Paroxysmal Nocturnal Hemoglobinuria | Urea Cycle Disorder | Mucormycosis | Chronic Lymphocytic Leukemia | Canavan Disease | Diffuse Intrinsic Pontine Glioma | Trachoma | Spinocerebellar Ataxia Type 7 | Metabolic Diseases | Endometriosis | Epicondylitis | Huntington's Disease | Hepatitis A | Antiphospholipid Syndrome | 3-M Syndrome | Juvenile Xanthogranuloma | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Poretti-Boltshauser Syndrome | Botulism | Cholestasis | Focal Segmental Glomerulosclerosis | Antisynthetase Syndrome | Familial Mediterranean Fever | Globozoospermia | Papillorenal Syndrome | Juvenile Myelomonocytic Leukemia | Episodic Ataxia Type 2 | Fetal And Neonatal Alloimmune Thrombocytopenia | Hepatic Steatosis | Blepharospasm | Currarino Syndrome | Diverticulitis | Pearson Syndrome | Anuria | Anxiety Disorders | Renal Hypouricemia | Myasthenia Gravis | Peeling Skin Syndrome, Acral Type | Turner's Syndrome | Stroke, Hemorrhagic | Pseudohypoparathyroidism Type 1B | Sponastrime Dysplasia | Cri-du-chat Syndrome | Microphthalmia, Syndromic 7 | Lateral Meningocele Syndrome | Leprosy | Heavy Chain Disease | Corticobasal Syndrome | Neovascular Glaucoma | Galactosialidosis | Facioscapulohumeral Muscular Dystrophy Type 2 | Spinal Muscular Atrophy Type 2 | Familial Hypertrophic Cardiomyopathy | Porokeratosis | 5-oxoprolinase Deficiency | Ebstein Anomaly | Keratoacanthoma | Chronic Neutrophilic Leukemia | Smoldering Myeloma | Pheochromocytoma | Pneumococcal Meningitis | Pitt-Hopkins Syndrome | Hemolytic Uremic Syndrome, Atypical | Sleep Apnea | Acquired Partial Lipodystrophy | Mitochondrial DNA Depletion Syndrome | Renal Oncocytoma | Combined Pituitary Hormone Deficiency | Hepatitis C, Chronic | Peters-plus Syndrome | Down Syndrome | Extramammary Paget's Disease | Glioma | Tonsillitis | Hereditary Spastic Paraplegia | Corneal Dystrophy And Perceptive Deafness | Chloridorrhea, Congenital | Nutrition Disorders | Schwannoma | Ependymoma | Keloid | Rift Valley Fever | Charcot-Marie-Tooth Disease Type 4E | Alopecia | Meconium Ileus | Pemphigus Vulgaris | Glycogen Storage Disease Type 0, Muscle | LEOPARD Syndrome | Blomstrand Osteochondrodysplasia | Myelitis, Transverse | Autonomic Nervous System Disorders | Spinocerebellar Ataxia | Transcobalamin Deficiency | Restless Legs Syndrome | Campomelic Dysplasia | Schwannomatosis | Acromegaly | Bloom Syndrome | Auriculocondylar Syndrome | Macular Corneal Dystrophy Type 1 | Eclampsia | Waardenburg Syndrome | Ganglioneuroma | Cancer, Breast | LMNA-related Congenital Muscular Dystrophy | Retinal Detachment | ICF Syndrome | Blue Rubber Bleb Nevus Syndrome | Usher Syndrome Type III | Lymphoma, B-cell | Dysmorphophobia | Sarcoma | Hypotonia-cystinuria Syndrome | Albinism | Pneumothorax | Esophagitis, Eosinophilic | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Asphyxia Neonatorum | Conduct Disorder | Juvenile Myoclonic Epilepsy | Osteochondrosis | Hypotrichosis | Heterotopic Ossification | Hyperglycemia | Onchocerciasis | Epidermal Nevus Syndrome | Homocystinuria | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Osteogenesis Imperfecta Type IV | Sweet Syndrome | Hemophagocytic Lymphohistiocytosis | Primary Lateral Sclerosis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Waardenburg Syndrome Type 2E | Cold Agglutinin Disease | Schizotypal Personality Disorder | Dystonia-parkinsonism, X-linked | Retinal Dystrophy | Basal Ganglia Disease, Biotin-responsive | Branchiootorenal Syndrome | Temporal Lobe Epilepsy | Depression