Disease

Seasonal Mood Disorder

About the Disease
Major Depressive Disorder, also known as seasonal affective disorder, is related to anxiety and endogenous depression, and has symptoms including affective symptoms, behavioral symptoms and schizophrenic language. An important gene associated with Major Depressive Disorder is HTR2A (5-Hydroxytryptamine Receptor 2A), and among its related pathways/superpathways are Signal Transduction and Neuroscience. The drugs Fluvoxamine and Valsartan have been mentioned in the context of this disorder. Affiliated tissues include brain, prefrontal cortex and cortex, and related phenotypes are depression and behavior/neurological

Common Targets
HCRTR1 | HTR2B | GABA(A) receptor | HTR2A | SLC6A3

疾病靶点研报
Seasonal mood disorder

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

Other Diseases

Proctitis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Hyperinsulinism-hyperammonemia Syndrome | Intermittent Claudication | Spina Bifida | Neurodegeneration With Brain Iron Accumulation | Hemosiderosis | Erdheim-Chester Disease | Osmotic Demyelination Syndrome | Splenomegaly | Withdrawal Syndrome | Ellis-Van Creveld Syndrome | B-cell Chronic Lymphocytic Leukemia | Focal Segmental Glomerulosclerosis | Herpes Simplex Dermatitis | Supravalvular Aortic Stenosis | Spinocerebellar Ataxia Type 13 | Amish Infantile Epilepsy Syndrome | Traboulsi Syndrome | Actinomycetoma | Epidermolysis Bullosa Simplex, Generalized | PHARC Syndrome | Neuromyotonia | NDH Syndrome | Zellweger Syndrome | Spinocerebellar Ataxia Type 23 | Exocrine Pancreatic Insufficiency | Arthrogryposis | Beckwith-Wiedemann Syndrome | Acute Generalized Exanthematous Pustulosis | Hypogonadism | Persistent Fetal Circulation | Congenital Bile Acid Synthesis Defect | Amelogenesis Imperfecta | Hypogammaglobulinemia | Charcot-Marie-Tooth Disease Type 4B1 | Sensory Neuropathy | Carcinoma In Situ | Zollinger-Ellison Syndrome | Irritable Bowel Syndrome | Thrombosis | Congenital Disorders Of Glycosylation | Esophagitis | Congenital Diaphragmatic Hernia | Charcot-Marie-Tooth Disease, Type 2A | Retinal Telangiectasia | Hairy Cell Leukemia | Acute Kidney Injury | Spinal Muscular Atrophy Type 3 | Inflammatory Linear Verrucous Epidermal Nevus | Silver-Russell Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Agnathia-Otocephaly Complex | Autosomal Recessive Spastic Paraplegia Type 54 | Systemic Mastocytosis | Meleda Disease | Hypokalemia | Chudley-McCullough Syndrome | Spondylocarpotarsal Synostosis Syndrome | Dowling-Degos Disease | Benign Familial Infantile Seizures | Aromatic L-amino Acid Decarboxylase Deficiency | Chordoid Glioma | Influenza | Delayed Sleep Phase Syndrome | Polyneuropathy | Craniofrontonasal Syndrome | Lichen Planus | Hashimoto Thyroiditis | Goiter, Nodular | Thyrotoxic Periodic Paralysis | Pseudohypoparathyroidism Type 1A | Lymphoma, Mantle Cell | Charcot-Marie-Tooth Disease, Type 1A | Fowler's Syndrome | Hepatitis A | Obsessive-compulsive Disorder | Wieacker-Wolff Syndrome | Kawasaki Disease | Juvenile Xanthogranuloma | Spinocerebellar Ataxia Type 7 | Spinocerebellar Ataxia Type 2 | Polymyalgia Rheumatica | Tinea | Pyloric Stenosis, Infantile Hypertrophic | Facioscapulohumeral Muscular Dystrophy Type 1 | Vitiligo | Persistent Mullerian Duct Syndrome | Cystitis | Allergic Contact Dermatitis | Hereditary Hemorrhagic Telangiectasia | Myositis | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Oculocutaneous Albinism | Cole-Carpenter Syndrome | Pulmonary Alveolar Proteinosis | Chylomicron Retention Disease | Sickle Cell Disease | Vitamin D Deficiency | Hennekam Lymphangiectasia-lymphedema Syndrome | Congenital Ichthyosiform Erythroderma | Dyskeratosis Congenita | Renal Hypomagnesemia 3 | 3-M Syndrome | Seizures | Motion Sickness | Diffuse Palmoplantar Keratoderma | Multifocal Motor Neuropathy | Coronary Artery Disease | Proximal Symphalangism | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Adenomatoid Tumor | Neurotoxicity | Localized Scleroderma | HIBCH Deficiency | LMNA-related Congenital Muscular Dystrophy | Autoimmune Hemolytic Anemia | Infertility, Male | Anterior Segment Dysgenesis | Proteus Syndrome | Cysticercosis | Otitis Media | Neutrophilia | Trichuriasis | Steel Syndrome | Charcot-Marie-Tooth Disease, Type 6 | Peyronie's Disease | Blastoma, Pleuropulmonary | Hemophilia | REM Sleep Behavior Disorder | Lafora Disease | Myosin Storage Myopathy | Progressive Familial Intrahepatic Cholestasis Type 1 | Phenylketonuria II | Pathological Gambling | Tietze Syndrome | Primary Biliary Cholangitis | Retinal Vasculitis | Reticular Dysgenesis | Neuroectodermal Tumors, Primitive | Cancer, Kidney | Brooke-Spiegler Syndrome | Infertility | Fragile X Syndrome | Hypolipoproteinemia | Esophageal Motility Disorders | Roberts Syndrome | Geleophysic Dysplasia | Crimean-Congo Hemorrhagic Fever | Glutaric Aciduria Type 3 | Progressive Familial Intrahepatic Cholestasis Type 3 | Alopecia | Polymyositis | Hepatitis D | Liddle Syndrome | Corneal Dystrophy | Cousin Syndrome | Botulism | Budd-Chiari Syndrome | Myoclonic Atonic Epilepsy | Adenocarcinoma | Smith-Magenis Syndrome | Lymphoma | Macular Corneal Dystrophy Type 1 | Anorchia | Cholera | Pancytopenia | Richter's Syndrome | Cryptorchidism | Chronic Neutrophilic Leukemia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Spinal And Bulbar Muscular Atrophy | Birk-Barel Syndrome | Calcium Pyrophosphate Deposition Disease | Cranial Nerve Disease | Kabuki Syndrome 2 | Corneal Neovascularization | Guanidinoacetate Methyltransferase Deficiency | Hypotension, Orthostatic | Iron Deficiency Anemia | Benign Familial Pemphigus | CHARGE Syndrome | Pitt-Hopkins Syndrome | Veno-occlusive Disease | Pneumonia, Viral | Generalized Epilepsy With Febrile Seizures Plus | Hemangioblastoma | Pemphigus Foliaceus | Canavan Disease | Thyroid Dysgenesis | Pontocerebellar Hypoplasia Type 2 | Nager Acrofacial Dysostosis | Leukodystrophies | Angiosarcoma | Chronic Granulomatous Disease, X-linked | Paroxysmal Kinesigenic Dyskinesia | Polycystic Ovary Syndrome | Periodontitis | Congenital Generalized Lipodystrophy | Gastroenteritis, Eosinophilic | Blomstrand Osteochondrodysplasia | Multiple Epiphyseal Dysplasia | Niemann-Pick Disease, Type C | GM2-gangliosidosis AB Variant | Polycystic Kidney, Autosomal Recessive | Pseudohypoaldosteronism | Osteoporosis, Postmenopausal | Arthritis, Reactive | Osteomyelitis | Autonomic Nervous System Disorders | Autosomal Recessive Congenital Ichthyosis | Ehlers-Danlos Syndrome | Chorioretinitis | Intellectual Disability, Autosomal Dominant 5 | Fuchs Dystrophy | Transient Bullous Dermolysis Of The Newborn | Fahr Disease | Dental Caries | Tricho-hepato-enteric Syndrome | Lichen Sclerosus | Acanthosis Nigricans | Poirier-Bienvenu Neurodevelopmental Syndrome | Incontinentia Pigmenti | Familial Pheochromocytoma-paraganglioma | Partington Syndrome | Bronchiolitis | Spinocerebellar Ataxia Type 21 | Sarcoma, Endometrial Stromal | Gynecomastia | Hyperandrogenemia | Leprosy | Dentinogenesis Imperfecta | Gingivitis | Leukocyte Adhesion Deficiency Type 1 | Tibial Muscular Dystrophy | Yellow Fever | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Pancreatitis, Chronic | Isobutyryl-CoA Dehydrogenase Deficiency | Cushing Syndrome | Melanoma | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Rift Valley Fever | Premature Ejaculation | Vogt-Koyanagi-Harada Syndrome | T-cell Prolymphocytic Leukemia | Congenital Mirror Movements | Sialidosis Type I | Primary Familial Brain Calcification | Aceruloplasminemia | Keratitis | Conjunctivitis, Allergic | Donnai-Barrow Syndrome | Becker Muscular Dystrophy | Giant Axonal Neuropathy | McKusick Type Metaphyseal Chondrodysplasia | Pleomorphic Xanthoastrocytoma | Shwachman-Bodian-Diamond Syndrome | Heart Septal Defects | Dementia, Vascular | Coronary Restenosis | Pachyonychia Congenita | Facioscapulohumeral Muscular Dystrophy | Congenital Aniridia | Intracranial Hypertension | Familial Thoracic Aortic Aneurysm | Epidermolysis Bullosa Acquisita | Vulvovaginitis | Carcinoid Syndrome | Christianson Syndrome | Emery-Dreifuss Muscular Dystrophy | Carcinoid Tumor | Hepatitis, Autoimmune | Guttate Psoriasis | Epithelial-myoepithelial Carcinoma | Onchocerciasis | Congenital Dyserythropoietic Anemia Type 4 | Asperger Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Ataxia-ocular Apraxia 2 | Glycogen Storage Disease Type 0, Muscle | Lentigo | Martsolf Syndrome | Intestinal Obstruction | Glaucoma | Fabry's Disease | Sepiapterin Reductase Deficiency | Occipital Neuralgia | Bardet-Biedl Syndrome | Lactose Intolerance | Costello Syndrome | Cervical Dystonia | Hoyeraal-Hreidarsson Syndrome | Pontocerebellar Hypoplasia Type 7 | Pyruvate Dehydrogenase Deficiency | Aplasia Cutis Congenita | Gastrointestinal Disorders | Hepatic Steatosis | Myotonia | Williams Syndrome | Peripheral T-cell Lymphoma | Chediak-Higashi Syndrome | VACTERL Association | Optic Nerve Diseases | Waardenburg Syndrome Type 1 | Neural Tube Defect | Hydrocephalus | Carpenter Syndrome | Oculodentodigital Dysplasia | Kleine-Levin Syndrome | Hemangioma | Angelman Syndrome | Long QT Syndrome Type 1 | Hydronephrosis | Proteasome-associated Autoinflammatory Syndrome 2 | Pleural Tuberculosis | Fuchs Heterochromic Iridocyclitis | Acute Leukemia | Eosinophilia | Renal Hypouricemia | Hyperferritinemia-cataract Syndrome | COACH Syndrome | Hodgkin Lymphoma | Rolandic Epilepsy | Xeroderma Pigmentosum | DRESS Syndrome | Glycogen Storage Disease Type 6 | Carbamoyl Phosphate Synthetase I Deficiency | Primary Lateral Sclerosis | Sturge-Weber Syndrome | Cannabis Abuse | 3-methylglutaconic Aciduria Type IV | Miyoshi Myopathy | Cavitary Optic Disc Anomalies | Blepharophimosis Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Personality Disorders | Schaaf-Yang Syndrome | Neurofibroma | Acral Lentiginous Melanoma | Porphyria, Acute Intermittent | Hernia, Inguinal | Gilbert Syndrome | Malignant Fibrous Histiocytoma | X-linked Acrogigantism | Krabbe Disease | Exfoliative Dermatitis | Myopathy | Chanarin-Dorfman Syndrome | Spinocerebellar Ataxia Type 17 | Metachondromatosis | Achromatopsia | Sporadic Hemiplegic Migraine | Vitreoretinal Degeneration, Snowflake Type | Parkinson Disease 6, Autosomal Recessive Early-onset | Autosomal Recessive Spastic Paraplegia Type 75 | Metachromatic Leukodystrophy | Hyperammonemia | Acquired Partial Lipodystrophy | Retinal Dystrophy, Early-onset Severe | Pemphigoid | Crouzon Syndrome With Acanthosis Nigricans | Mucolipidosis Type IV | Parkinson's Disease | Diastrophic Dysplasia | Discoid Lupus Erythematosus | Hereditary Spherocytosis | T-cell Leukemia | Chylothorax, Congenital | Mitochondrial Encephalomyopathy | Nijmegen Breakage Syndrome | Myocarditis | Purpura | Oligospermia | Sclerosteosis | Riboflavin Transporter Deficiency Neuronopathy | Blood Protein Disorders | Leiomyoma | Dysfibrinogenemia | Mesothelioma, Malignant | Lymphangioleiomyomatosis | Cabezas Syndrome | Mitochondrial DNA Depletion Syndrome | Bronchitis, Chronic | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Congenital Hereditary Endothelial Dystrophy Type I | Lipid Storage Diseases | Ulcerative Colitis | Insulinoma | Analgesia | Pituitary Stalk Interruption Syndrome | Melanoma, Uveal | Jawad Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Pneumococcal Meningitis | Rhabdoid Tumor | Primary Carnitine Deficiency | Azoospermia | Carcinoma, Merkel Cell | Eclampsia