Disease

Narcolepsy

About the Disease
Narcolepsy, also known as narcoleptic syndrome, is related to narcolepsy 1 and cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, and has symptoms including hemiplegia, sleep disturbances and snoring. An important gene associated with Narcolepsy is HCRT (Hypocretin Neuropeptide Precursor), and among its related pathways/superpathways are Transcription factor regulation in adipogenesis and Orexin receptor pathway. The drugs Central Nervous System Stimulants and Sodium citrate have been mentioned in the context of this disorder. Affiliated tissues include brain, heart and eye.

Common Targets
HNMT | G7124 | PER2 | CCR3 | Glutamate Receptor Ionotropic AMPA Receptor | G5243 | HLA-C | SCN5A | HRH3 | HLA-DQB1 | HCRT | SNORD105 | PPAN | Phosphodiesterase 1 (PDE1) (nonspecified subtype) | Gamma-Aminobutyric acid type B receptor | NPSR1 | PDE1C | Alpha-2 Adrenergic receptors (nonspecified subtype) | CHKB-DT | Calcium channel (nonspecified subtype) | HLA-DQA1 | HCRTR1 | CPT1B | NFATC2 | EIF3G | P2RY11 | HTR2B | SLC6A2 | HLA-B | CACNA1C | SCP2 | DRD2 | Nicotinic alpha4beta2 receptor | GABA(A) receptor | CTSH | HLA-DRB1 | ADRA2A | OPRL1 | HLA-DPA1 | CHKB | ADORA2A | CHKB-CPT1B | PTGDR | HCRTR2 | ADRB1 | ACHE | DRD1 | GSK3B | HLA-A | TRIB2 | PDE1B | CCR1 | HTR1B | alpha1-Adrenoceptor (nonspecified subtype) | SLC6A4 | HLA-DPB1 | NMDA receptor | APP | G1786 | HTR2C | MCHR1 | PDE1A | CHRNB2 | TAAR1 | SLC6A3

疾病靶点研报
Narcolepsy

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

Other Diseases

Osteogenesis Imperfecta | Impulse Control Disorder | Colon Adenoma | Esophageal Carcinoma | Lentigo | Glomerulonephritis, Membranous | Evans Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Nemaline Myopathy 8 | Pyruvate Kinase Deficiency | Chronic Myeloid Leukemia | Smoldering Myeloma | Usher Syndrome Type IIC | Neurodevelopmental Disorders | Neonatal Progeroid Syndrome | Microvillus Inclusion Disease | Dermatitis Herpetiformis | Osteomyelitis | Hydrocephalus | Phosphoglycerate Dehydrogenase Deficiency | Inflammatory Bowel Disease | Congenital Adrenal Hyperplasia | Ophthalmia, Sympathetic | Myocardial Infarction | Rhinitis | Glycogen Storage Disease Type 6 | Hepatic Veno-occlusive Disease | Crimean-Congo Hemorrhagic Fever | Waardenburg Syndrome | Micro Syndrome | Myasthenia Gravis | Angiomyolipoma | Bursitis | Osteitis | Cryopyrin-associated Periodic Syndromes | Coloboma | Pierson Syndrome | Dupuytren Disease | Facioscapulohumeral Muscular Dystrophy Type 2 | Charcot-Marie-Tooth Disease Type 2D | Ventricular Septal Defect | Nephrotic Syndrome | Ehlers-Danlos Syndrome | Fanconi Syndrome | Thyroiditis, Autoimmune | Platelet Disorders | Uremic Pruritus | Hypermethioninemia | Cellulitis | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Systemic Lupus Erythematosus | Coffin-Siris Syndrome | Meleda Disease | Multiple Sclerosis, Primary Progressive | Anencephaly | Neuroleptic Malignant Syndrome | Kallmann Syndrome | Blepharoconjunctivitis | Polyomavirus Nephropathy | Pouchitis | Hyperkalemic Periodic Paralysis | Porokeratosis | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Melanoma, Uveal | POEMS Syndrome | Intellectual Disability, Autosomal Dominant 5 | Meesmann Corneal Dystrophy | Pathological Gambling | Pseudoexfoliation Syndrome | Hypocalcemia | Vitamin K Deficiency | Spinocerebellar Ataxia Type 27 | Cardiospondylocarpofacial Syndrome | Genitopatellar Syndrome | Walker-Warburg Syndrome | Tyrosinemia Type 2 | Osteoporosis, Postmenopausal | C3 Glomerulonephritis | Cholestasis | Usher Syndrome Type I | COACH Syndrome | CHARGE Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Menetrier Disease | Scleritis | Carpal Tunnel Syndrome | Keratosis, Seborrheic | Eiken Syndrome | Gastroenteritis | Desbuquois Syndrome | Renal Dysplasia | Esotropia | Inflammatory Myopathy | Optic Neuropathy | Rhizomelic Chondrodysplasia Punctata | Spinocerebellar Ataxia Type 13 | Esophageal Adenocarcinoma | Atopic Dermatitis | Epidermolysis Bullosa Dystrophica | Chronic Idiopathic Myelofibrosis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Marinesco-Sjogren Syndrome | Intestinal Hypomagnesemia 1 | Fundus Albipunctatus | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Osteochondrosis | Nager Acrofacial Dysostosis | Congenital Primary Aphakia | Heterotaxy | McCune-Albright Syndrome | Hypertension | Bietti Crystalline Dystrophy | Sezary Syndrome | Epidermolysis Bullosa Simplex, Generalized | Multiple Sclerosis, Secondary Progressive | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Nephritis, Interstitial | Ganglioneuroma | Schnitzler Syndrome | Iron Overload | Johanson-Blizzard Syndrome | Liver Diseases | Paroxysmal Kinesigenic Dyskinesia | Portal Vein Thrombosis | Hepatitis, Alcoholic | Dermatofibrosarcoma | Cryptococcal Meningitis | KBG Syndrome | Sorsby Fundus Dystrophy | Macrodactyly | Thyrotoxic Periodic Paralysis | Osteogenesis Imperfecta Type VI | Schindler Disease | Thyroid Hormone Resistance | Kawasaki Disease | Coma | Norrie Disease | Iron Metabolism Disorders | Carcinoma, Squamous Cell | Stargardt Disease | Endometrial Hyperplasia | Dentinogenesis Imperfecta | Tardive Dyskinesia | Inflammatory Joint Disease | Osteoporosis | Adenoma, Pleomorphic | Lymphoma, B-cell | Duane Retraction Syndrome | Pre-eclampsia | Chronic Granulomatous Disease, X-linked | Hartnup Disease | Hemochromatosis | Pancreatitis, Chronic | Polyarteritis Nodosa | Keratoconus | Pneumoconiosis | Lymphopenia | Dowling-Degos Disease | Chromosome 5q Deletion Syndrome | Traboulsi Syndrome | Rett Syndrome | Connective Tissue Disorders | Leukoencephalopathy, Progressive Multifocal | Learning Disability | Epidermodysplasia Verruciformis | Basal Ganglia Disease | Hypersomnia | Peutz-Jeghers Syndrome | Thyroid Dysgenesis | Carney-Stratakis Syndrome | Lathosterolosis | Fatty Aldehyde Dehydrogenase Deficiency | Acute Chest Syndrome | Vaginitis | Congenital Dyserythropoietic Anemia | Dermatomyositis | Mannosidase Deficiency Diseases | Acral Lentiginous Melanoma | 3-hydroxy-3-methylglutaric Aciduria | Schizophrenia, Paranoid | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Placenta Previa | Chondroma | Methylmalonic Acidemia | Waldenstrom Macroglobulinemia | Amenorrhea | Myhre Syndrome | CDKL5 Deficiency Disorder | Compartment Syndrome | Anti-glomerular Basement Membrane Disease | Renal-hepatic-pancreatic Dysplasia | Botulism | Thrombophilia | Pleomorphic Xanthoastrocytoma | Agranulocytosis | Spinocerebellar Ataxia Type 40 | Hyperprolactinemia | Osteogenesis Imperfecta Type I | 3-methylglutaconic Aciduria Type IV | Encephalitis | Microphthalmia | VACTERL/VATER Association | Congenital Absence Of Vas Deferens | Gastroenteritis, Eosinophilic | Orotic Aciduria | Treacher Collins Syndrome | Heterotopic Ossification | Keratoacanthoma | Focal Facial Dermal Dysplasia | Tietze Syndrome | Thymoma, Malignant | Schistosomiasis | Metatropic Dysplasia | Richter's Syndrome | Ocular Hypertension | Retinal Degeneration | Heroin Dependence | Pupil Disorders | Robinow Syndrome | Stickler Syndrome | Anorchia | Nijmegen Breakage Syndrome | Chronic Neutrophilic Leukemia | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Postpartum Depression | Tinea Versicolor | Syphilis | Chromosome 8q21.11 Deletion Syndrome | Myasthenia | Autonomic Nervous System Disorders | Cartilage Disorders | Bacterial Meningitis | Sporadic Inclusion Body Myositis | Choroiditis | Rhabdomyosarcoma | Primary Progressive Aphasia | Diabetic Macular Edema | Thrombocytopenia | Apparent Mineralocorticoid Excess Syndrome | Hepatitis, Autoimmune | Adult Polyglucosan Body Disease | Coffin-Lowry Syndrome | Amelanotic Melanoma | Polycythemia Vera | Pancreatitis | Behavioral Variant Of Frontotemporal Dementia | Renal Oncocytoma | Renpenning Syndrome | Ulcerative Colitis | Renal Hypomagnesemia 3 | Hennekam Lymphangiectasia-lymphedema Syndrome | WAGR Syndrome | Acute Leukemia | Hypothyroidism | Chondromyxoid Fibroma | Cryoglobulinemia | Encephalopathy, Hepatic | Alpers Syndrome | Larsen Syndrome | Hernia, Inguinal | Hemorrhoids | Meniere's Disease | IMAGe Syndrome | Hyperparathyroidism, Primary | Pure Red Cell Aplasia | Vascular Calcification | Familial Pheochromocytoma-paraganglioma | Rift Valley Fever | Apraxia | Hereditary Hemorrhagic Telangiectasia Type 2 | Gangliosidosis | Hodgkin Lymphoma | Lactose Intolerance | Tatton-Brown-Rahman Syndrome | Ghosal Syndrome | Parkinson's Disease | Spinocerebellar Ataxia Type 23 | Blood Protein Disorders | Cushing Syndrome | Actinomycetoma | Hypoalbuminemia | Urea Cycle Disorder | Pernicious Anemia | Adenomyosis | Intermittent Claudication | Stuve-Wiedemann Syndrome | Nephropathy | Rhabdomyosarcoma, Embryonal | Tenosynovial Giant Cell Tumor | Acute Lymphocytic Leukemia | Pycnodysostosis | Thyroid Dyshormonogenesis | Cataract | Primary Familial Brain Calcification | Pleurisy | PHARC Syndrome | Hyperparathyroidism | Congenital Dyserythropoietic Anemia Type 4 | Hyperphenylalaninemia | Porencephaly | Mevalonate Kinase Deficiency | Pregnancy, Ectopic | Crouzon Syndrome With Acanthosis Nigricans | Fibromuscular Dysplasia | HELLP Syndrome | Hypoplastic Left Heart Syndrome | Paraganglioma | Schizotypal Personality Disorder | Familial Isolated Hyperparathyroidism | Conduct Disorder | Uveitis, Anterior | Familial Hyperaldosteronism | Epidermal Nevus Syndrome | Vulvovaginitis | Neurofibroma, Plexiform | Acute Coronary Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Gilbert Syndrome | Plasma Cell Dyscrasia | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Spondylometaphyseal Dysplasia | Alkaptonuria | Diverticulitis | Schwartz-Jampel-Aberfeld Syndrome | Achondrogenesis | Werner's Syndrome | Polycythemia | Exostoses | Panniculitis | Wiskott-Aldrich Syndrome | Sialoadenitis | Congenital Sodium Diarrhea | Duodenal Atresia | Acute Motor Axonal Neuropathy | Silicosis | Necrotizing Autoimmune Myopathy | Molybdenum Cofactor Deficiency | Spinal Muscular Atrophy | Autoimmune Polyendocrinopathy Syndrome Type I | Amebiasis | Retinal Telangiectasia | Synpolydactyly | Dengue Shock Syndrome | Olmsted Syndrome | N-acetylglutamate Synthase Deficiency | Adrenoleukodystrophy, X-linked | Personality Disorders | Schamberg Disease | Bone Giant Cell Tumor | Myelomeningocele | DEND Syndrome | Lamellar Ichthyosis | Ocular Albinism Type 1 | Spinocerebellar Ataxia Type 12 | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Kabuki Syndrome 2 | Carey-Fineman-Ziter Syndrome | Granular Corneal Dystrophy Type 1 | Bipolar Disorder | Carcinoid Tumor | Jalili Syndrome | Osteoglophonic Dysplasia | Hemangioblastoma | Glycogen Storage Disease Type 4 | Keratocystic Odontogenic Tumor | Gaucher Disease | Williams Syndrome | Endocarditis | Malaria | Dyslexia | Tremor | Blau Syndrome | Albinism | LMNA-related Congenital Muscular Dystrophy | Cranioectodermal Dysplasia | Sickle Cell Disease | Pulmonary Veno-occlusive Disease | Erythrokeratodermia Variabilis | Stevens-Johnson Syndrome | Colitis | Nevus | Marshall-Smith Syndrome | Fibrillation, Atrial | Seizures | Myositis, Focal | Diabetic Encephalopathy | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Erythema Nodosum | Pineoblastoma | Bare Lymphocyte Syndrome | Amyotrophic Lateral Sclerosis, Juvenile | Coronary Artery Disease | Costello Syndrome | Charcot-Marie-Tooth Disease Type 3 | Fabry's Disease | Myocarditis | Ichthyosis Bullosa Of Siemens | Spinocerebellar Ataxia Type 17 | T-cell Chronic Lymphocytic Leukemia | Rosacea