Schizoaffective Disorder
Schizoaffective Disorder
About the Disease
Schizoaffective Disorder, also known as schizophreniform psychosis, affective type, is related to schizophrenia 18 and schizophrenia 2. An important gene associated with Schizoaffective Disorder is DISC2 (Disrupted In Schizophrenia 2), and among its related pathways/superpathways are Neuroscience and Neuroinflammation and glutamatergic signaling. The drugs Donepezil and Guanfacine have been mentioned in the context of this disorder. Affiliated tissues include prefrontal cortex, brain and cortex, and related phenotypes are nervous system and homeostasis/metabolism
Common Targets
G3569 | BDNF | DAO | CHRM4 | OPRK1 | ACE | DISC1 | HCRTR1 | DRD2 | COMT | SLC6A9 | HTR1A | GABRR1 | DTNBP1 | PROKR1 | CALR | HTR2A

Note: If you'd like to get a target analysis report for Schizoaffective 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 Schizoaffective Disorder at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Blomstrand Osteochondrodysplasia | Hodgkin Lymphoma | Hereditary Mixed Polyposis Syndrome | Niemann-Pick Disease | Spinocerebellar Ataxia | Trichotillomania | Encephalitis, Tick-borne | Neurogenic Bladder | Pituitary Dwarfism | Anorchia | Cardiac Arrest | Spinocerebellar Ataxia Type 27 | Ovarian Hyperstimulation Syndrome | Cholecystitis | Allan-Herndon-Dudley Syndrome | Melanocytic Nevus | Spinocerebellar Ataxia Type 6 | Arrhythmogenic Right Ventricular Cardiomyopathy | Pleural Tuberculosis | Malaria | Milk Allergy | Primary Hyperoxaluria | Sclerosteosis 2 | Methylmalonic Acidemia | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Pterygium | Hereditary Spastic Paraplegia | Thyroid Dysgenesis | Aplasia Cutis Congenita | Varicocele | Pulmonary Sclerosing Hemangioma | Mandibuloacral Dysplasia With Type A Lipodystrophy | Mabry Syndrome | Tibial Muscular Dystrophy | Chromosome 5q Deletion Syndrome | Arteriovenous Malformations | Dwarfism | VEXAS Syndrome | Osteoporosis | Corticobasal Syndrome | Thyroiditis, Autoimmune | Alopecia Areata | Autosomal Recessive Spastic Paraplegia Type 54 | Polymyositis | Hyperinsulinemic Hypoglycemia | Myotonia | Glycogen Storage Disease Type 5 | Bainbridge-Ropers Syndrome | Oligospermia | Fetal Akinesia Deformation Sequence | Transient Bullous Dermolysis Of The Newborn | Leiomyoma | Prolactinoma | Chromosome 16p11.2 Deletion Syndrome | DRESS Syndrome | Erythropoietic Protoporphyria | Still Disease | Phenylketonuria | Argininosuccinic Aciduria | Chondrosarcoma | Mosaic Variegated Aneuploidy Syndrome 2 | Schizophrenia | Chronic Myeloid Leukemia | Bronchitis | Malnutrition | Melanoma, Malignant | Spastic Paraplegia Type 7 | Nephritis, Interstitial | Nephronophthisis | Calcium Pyrophosphate Deposition Disease | Mast Cell Leukemia | Spinal Muscular Atrophy | Huntington's Disease | Peyronie's Disease | Carey-Fineman-Ziter Syndrome | T-cell Prolymphocytic Leukemia | Lymphoproliferative Disease, X-linked | Oligoasthenoteratozoospermia | Adams-Oliver Syndrome | Schwannomatosis | Chromosome 17q21.31 Deletion Syndrome | Vici Syndrome | Measles | Familial Advanced Sleep Phase Syndrome | Chloridorrhea, Congenital | Absence Epilepsy | Usher Syndrome Type III | Common Variable Immunodeficiency | Restrictive Dermopathy | Basal Ganglia Cerebrovascular Disease | Asphyxia Neonatorum | Anterior Segment Dysgenesis | Hepatitis E | Cri-du-chat Syndrome | Vogt-Koyanagi-Harada Syndrome | Nicotine Addiction | Protein C Deficiency | Acromegaly | Carney-Stratakis Syndrome | Ventricular Septal Defect | Gigantism | Sickle Cell Anemia | Holt-Oram Syndrome | Takayasu's Arteritis | Hepatitis A | Wagner Disease | Frontotemporal Dementia | Phosphoglycerate Dehydrogenase Deficiency | Pseudo-pseudohypoparathyroidism | Choriocarcinoma | Precocious Puberty | Acromesomelic Dysplasia | Cerebrotendinous Xanthomatosis | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Epidermolysis Bullosa | Lymphedema | Lysosomal Acid Lipase Deficiency | Thrombasthenia | Rotor Syndrome | Hypospadias | REM Sleep Behavior Disorder | Auriculocondylar Syndrome | HIBCH Deficiency | Dystonia Musculorum Deformans | Systemic Mastocytosis | Hereditary Elliptocytosis | Craniofacial Dysostosis | Primary Carnitine Deficiency | Congenital Heart Block | Clouston Hidrotic Ectodermal Dysplasia | Shock, Cardiogenic | Microvillus Inclusion Disease | Situs Inversus | LRBA Deficiency | Epidermolysis Bullosa Acquisita | Primary Hyperoxaluria Type 1 | Papilledema | Eosinophilia | Plasma Cell Dyscrasia | Congenital Fiber-type Disproportion Myopathy | Sarcomatoid Carcinoma Of The Lung | Osteogenesis Imperfecta Type V | Multiple System Atrophy | Spermatocele | Osteogenesis Imperfecta Type IV | Congenital Dyserythropoietic Anemia | Autoimmune Polyendocrinopathy Syndrome Type I | Prolymphocytic Leukemia | Marinesco-Sjogren Syndrome | Seizures | Muscular Dystrophy | Low Tension Glaucoma | Triple A Syndrome | Familial Pheochromocytoma-paraganglioma | Anorectal Malformations | Hairy Cell Leukemia | Adult Polyglucosan Body Disease | Alopecia | Recurrent Respiratory Papillomatosis | Congenital Torticollis | Oculocutaneous Albinism Type 1 | CEDNIK Syndrome | Congenital Tufting Enteropathy | Rubinstein-Taybi Syndrome | Pure Red Cell Aplasia | Ataxia-ocular Apraxia 2 | Neurodevelopmental Disorders | Seborrheic Dermatitis | Supravalvular Aortic Stenosis | Tietze Syndrome | Leukemia | Idiopathic Multicentric Castleman Disease | Cholestasis, Intrahepatic | Swine Influenza | Hyperparathyroidism, Primary | Blepharospasm | Hashimoto Thyroiditis | Thalassemia | Hernia, Inguinal | X-linked Myotubular Myopathy | Familial Hemiplegic Migraine | Polyradiculopathy | Hidradenitis | Vulvovaginitis | Thymoma, Malignant | Fuchs Dystrophy | Mitochondrial Disease | Osmotic Demyelination Syndrome | Hyperparathyroidism, Secondary | Creatine Deficiency Syndrome | Familial Thoracic Aortic Aneurysm | Nemaline Myopathy 10 | Aicardi-Goutieres Syndrome | Pneumonia, Mycoplasma | Hyperferritinemia-cataract Syndrome | Kawasaki Disease | Cole-Carpenter Syndrome | Retinal Vasculitis | Haim-Munk Syndrome | Gastroenteritis | Pearson Syndrome | Gastritis | Triphalangeal Thumb-polysyndactyly Syndrome | Hereditary Spherocytosis | Meckel-Gruber Syndrome | Leukodystrophies | Sturge-Weber Syndrome | Carcinoma, Transitional Cell | Epithelial-myoepithelial Carcinoma | Hypertension, Pulmonary | Keloid | Hemosiderosis | Epidermolysis Bullosa Simplex, Generalized | Cluster Headache | Autosomal Recessive Spastic Paraplegia Type 35 | Stomatitis | Conjunctivitis | Carcinoma, Merkel Cell | Hypobetalipoproteinemias | Hamartoma | Cold-induced Sweating Syndrome | Fatty Aldehyde Dehydrogenase Deficiency | Harlequin Ichthyosis | Thanatophoric Dysplasia Type 1 | Crigler-Najjar Syndrome | Short-chain Acyl-CoA Dehydrogenase Deficiency | Chitayat Syndrome | Orotic Aciduria | Language Disorders | Pneumococcal Meningitis | Vertebrobasilar Insufficiency | Sitosterolemia | Exotropia | Ectopia Lentis, Isolated, Autosomal Recessive | Proctitis | Albinism | Cryptorchidism | Peeling Skin Syndrome Type B | Weill-Marchesani Syndrome | Portal Vein Thrombosis | Gardner Syndrome | Glomerulonephritis | Pseudohypoparathyroidism Type 1B | Dermatofibrosarcoma | Neurofibromatosis | Evans Syndrome | Genee-Wiedemann Syndrome | COACH Syndrome | Patent Ductus Arteriosus | Cysticercosis | Oral Lichen Planus | Nance-Horan Syndrome | Familial Mediterranean Fever | Waardenburg Syndrome Type 2 | Hypercholesterolemia, Familial | Down Syndrome | Cardiospondylocarpofacial Syndrome | Pyruvate Decarboxylase Deficiency | Encephalocele | Chromosome 8q21.11 Deletion Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Kaposiform Hemangioendothelioma | Myosin Storage Myopathy | Nephropathy | Lymphoma | Silicosis | Pernicious Anemia | Charcot-Marie-Tooth Disease Type 4D | Pontocerebellar Hypoplasia Type 2 | Smith-Kingsmore Syndrome | Persistent Fetal Circulation | Enterocolitis, Necrotizing | Nephrosclerosis | CREST Syndrome | Brachydactyly | Brooke-Spiegler Syndrome | Oculocutaneous Albinism | Filariasis | Polymyalgia Rheumatica | Neuronal Ceroid Lipofuscinosis | Odonto-onycho-dermal Dysplasia | Interstitial Lung Diseases | Acute Myeloid Leukemia | Noonan Syndrome-like Disorder With Loose Anagen Hair | Cancer, Colon | Barrett Esophagus | Pulmonary Veno-occlusive Disease | Long QT Syndrome Type 3 | Follicular Dendritic Cell Sarcoma | Benign Familial Neonatal Convulsions | Asthma, Exercise-induced | Addison Disease | Chordoid Glioma | Sepiapterin Reductase Deficiency | Glycogen Storage Disease Type 0 | Dystrophy, Cone-rod | Fibrillation, Atrial | Stromal Corneal Dystrophy | POEMS Syndrome | Atrial Septal Defect | Stiff-man Syndrome | Androgen Insensitivity | Antisynthetase Syndrome | Synpolydactyly | B-cell Prolymphocytic Leukemia | Cataplexy | Leukoplakia, Oral | Glycogen Storage Disease Type 4 | Hyperlipidemia Type V | Dengue Shock Syndrome | Spinocerebellar Ataxia Type 20 | Tracheal Disorders | Atopy | Charcot-Marie-Tooth Disease, Type 6 | Stroke | Alpha-thalassemia Myelodysplasia Syndrome | Majeed Syndrome | Hemolytic Uremic Syndrome, Atypical | DEND Syndrome | Congenital Aniridia | Pneumonia, Bacterial | Spina Bifida | Paronychia | Spondyloarthritis | Viral Meningitis | Rickets | Vestibular Disease | Rhinitis | Schwartz-Jampel-Aberfeld Syndrome | Peritonitis | Aspergillosis | Alpha-mannosidosis | Hypotrichosis Simplex | Polycystic Kidney, Autosomal Dominant | Campomelic Dysplasia | Glaucomatocyclitic Crisis | Asthma | Neovascular Glaucoma | Colitis, Lymphocytic | Dental Caries | Occipital Neuralgia | Dementia | Colitis, Microscopic | Fibromyalgia | Leiomyosarcoma | Hypoproteinemia, Hypercatabolic | Rhizomelic Chondrodysplasia Punctata | Von Willebrand Disease | Long QT Syndrome Type 1 | Apert Syndrome | GNE Myopathy | Fahr Disease | Nephrotic Syndrome | Arthritis, Gouty | Ollier Disease | Facioscapulohumeral Muscular Dystrophy Type 2 | Heavy Chain Disease | 5-oxoprolinase Deficiency | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Arthropathy | Phenylketonuria II | Mitochondrial Myopathy | Giant Cell Glioblastoma | Fascioliasis | Lymphoma, AIDS-related | Keratitis-ichthyosis-deafness Syndrome | Malonyl-CoA Decarboxylase Deficiency | Ichthyosis, X-linked | Angelman Syndrome | Renal Tubular Acidosis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Thyroid Dyshormonogenesis | Osteomalacia | Familial Hypertrophic Cardiomyopathy | Hydrops Fetalis | Acne | Bronchiectasis | Hyperparathyroidism-jaw Tumor Syndrome | Congenital Mirror Movements | Esthesioneuroblastoma | Gastroenteritis, Eosinophilic | Vascular Cognitive Impairment | Pupil Disorders | Mucolipidosis Type III | Hypolipoproteinemia | Panic Disorder | Lymphangioleiomyomatosis | Adenosine Deaminase 2 Deficiency | Angina Pectoris | Strabismus | 3C Syndrome | Lichen Sclerosus | Mitochondrial Encephalomyopathy | Cone Dystrophy | Lattice Corneal Dystrophy Type 1 | Cabezas Syndrome | Werner's Syndrome | Pemphigus Foliaceus | Fibronectin Glomerulopathy | Ebstein Anomaly