Disease

Familial Advanced Sleep Phase Syndrome

About the Disease
Advanced Sleep Phase Syndrome, also known as fasps, is related to advanced sleep phase syndrome, familial, 1 and sleep disorder. An important gene associated with Advanced Sleep Phase Syndrome is PER2 (Period Circadian Regulator 2), and among its related pathways/superpathways are Neuroscience and Circadian Clock. The drugs Melatonin and Protective Agents have been mentioned in the context of this disorder. Affiliated tissues include hypothalamus and brain, and related phenotypes are no effect and no effect

Common Targets
PER3

疾病靶点研报
Familial Advanced Sleep Phase Syndrome

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

Other Diseases

DiGeorge Syndrome | Paronychia | Retinopathy, Diabetic | Blepharitis | Inborn Errors Of Metabolism | Saul-Wilson Syndrome | Vertigo | Huntington's Disease-like 2 | Angiosarcoma | Congenital Heart Defects | Megaloblastic Anemia | Blau Syndrome | Pneumonia, Bacterial | Corneal Neovascularization | Senior-Loken Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Facioscapulohumeral Muscular Dystrophy Type 1 | Schamberg Disease | Osteomyelitis | Epilepsy Of Infancy With Migrating Focal Seizures | Cutaneous T-cell Lymphoma | Hereditary Spherocytosis | Impetigo | Cutaneous Mastocytosis | Tietze Syndrome | Pontocerebellar Hypoplasia | Intestinal Pseudo-obstruction | Hypopituitarism | Adenosine Deaminase Deficiency | Rhabdomyosarcoma, Embryonal | Tendinitis | Scabies | Chronic Leukemia | Cystitis | Hidradenitis Suppurativa | Usher Syndrome Type II | Ichthyosis Bullosa Of Siemens | Peeling Skin Syndrome Type B | Lewy Body Dementia | Optic Neuropathy, Anterior Ischemic | Sorsby Fundus Dystrophy | Aneurysm, Thoracic Aortic | Alpha-1 Antitrypsin Deficiency | Zollinger-Ellison Syndrome | Acromicric Dysplasia | Myasthenia Gravis | Endometritis | Sandhoff Disease | Aromatic L-amino Acid Decarboxylase Deficiency | Spinocerebellar Ataxia Type 20 | Lichen Sclerosus | Glaucomatocyclitic Crisis | Multiple Myeloma | Pendred Syndrome | Hyperacusis | Gastroschisis | Parapsoriasis | TARP Syndrome | Leukodystrophies | Crouzon Syndrome With Acanthosis Nigricans | Giant Cell Arteritis | Rubinstein-Taybi Syndrome | Porphyria, Acute Intermittent | Vici Syndrome | Eosinophilic Asthma | Zimmermann-Laband Syndrome | Vascular Cognitive Impairment | Ichthyosis Hystrix, Curth-Macklin Type | Carotid Artery Disease | Isobutyryl-CoA Dehydrogenase Deficiency | Mucormycosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Osteogenesis Imperfecta Type I | Cold-induced Sweating Syndrome | Trichomegaly | Conduct Disorder | Hennekam Lymphangiectasia-lymphedema Syndrome | Myhre Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Sclerosteosis 2 | Inflammatory Joint Disease | Tremor | Cutaneous Lupus Erythematosus | Bulimia Nervosa | Angioimmunoblastic T-cell Lymphoma | Barrett Esophagus | Paraplegia | Gliosarcoma | Renal Failure | Exocrine Pancreatic Insufficiency | Hypertension, Renovascular | Neutrophilia | Cholestasis | Congenital Disorders Of Glycosylation | Lipid Metabolism Disorders | Sitosterolemia | Desmosterolosis | Multiple Sclerosis, Primary Progressive | Molybdenum Cofactor Deficiency | Colitis | Gastroenteritis, Eosinophilic | Pelizaeus-Merzbacher Disease | Influenza | Cat Eye Syndrome | N-acetylglutamate Synthase Deficiency | Hermansky-Pudlak Syndrome | Prolactinoma | Colitis, Microscopic | Liver Diseases | Acute Kidney Injury | Hepatitis, Chronic | Dominant Optic Atrophy | Noonan Syndrome | D-2-Hydroxyglutaric Aciduria | Epidermodysplasia Verruciformis | Spondylolisthesis | Leukoplakia, Oral | Microphthalmia, Syndromic 7 | Lipid Storage Diseases | Pleural Tuberculosis | Duane Retraction Syndrome | Cousin Syndrome | Microvillus Inclusion Disease | VACTERL Association | Angiodysplasia | Sarcosinemia | Alpha-thalassemia Myelodysplasia Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Hydrops Fetalis | Colitis, Lymphocytic | Keratoacanthoma | Leukemia | Fibrosis | Intracerebral Hemorrhage | REM Sleep Behavior Disorder | Synpolydactyly | Dysplastic Nevus | Renal Dysplasia | Chromosome 9q34.3 Deletion Syndrome | Connective Tissue Disorders | Insulin Resistance | Craniolenticulosutural Dysplasia | Open-angle Glaucoma | Adult Polyglucosan Body Disease | Osteogenesis Imperfecta Type V | Chorioretinitis | Hyperhomocysteinemia | IMAGe Syndrome | Cabezas Syndrome | Neuromyotonia | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Ectodermal Dysplasia | Episodic Ataxia | Headache | Macular Degeneration | Tic Disorder | Glioma | Glaucoma | Androgen Insensitivity | Diffuse Palmoplantar Keratoderma | Coenzyme Q10 Deficiency | Hyperparathyroidism | Polyradiculopathy | Sleep Apnea, Central | Persistent Truncus Arteriosus | Hereditary Multiple Exostoses | Syncope | Charcot-Marie-Tooth Disease, Type 2A | Pupil Disorders | Pain | Neuroendocrine Cancer | Restless Legs Syndrome | Precocious Puberty | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Mosaic Variegated Aneuploidy Syndrome 2 | Familial Thoracic Aortic Aneurysm | Nicotine Dependence | C3 Glomerulopathy | Cranial Nerve Disease | Microcephaly, Seizures, And Developmental Delay | Autosomal Recessive Bestrophinopathy | Dwarfism | Rolandic Epilepsy | Renal-hepatic-pancreatic Dysplasia | Weill-Marchesani Syndrome | Cholestasis, Intrahepatic | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Sensorineural Hearing Loss | Congenital Generalized Lipodystrophy | Exotropia | Amelogenesis Imperfecta | Otopalatodigital Syndrome Type 2 | Trigonocephaly | Carcinoma, Signet Ring Cell | Pituitary Stalk Interruption Syndrome | Anorectal Malformations | Discoid Lupus Erythematosus | Netherton Syndrome | Hernia, Inguinal | Schnyder Crystalline Corneal Dystrophy | Pyoderma Gangrenosum | Neurodermatitis | Meier-Gorlin Syndrome | Muscular Dystrophy | Wolman Disease | Acute Coronary Syndrome | Majeed Syndrome | Hyperthermia, Malignant | Cleidocranial Dysplasia | Cancer, Prostate | Brugada Syndrome 1 | Craniofrontonasal Syndrome | Jaundice, Obstructive | Thrombosis | Ganglioglioma | Congenital Diaphragmatic Hernia | Nanophthalmos | Amish Infantile Epilepsy Syndrome | Lichen Planus | Hereditary Inclusion Body Myopathy | Stroke, Hemorrhagic | Macrophagic Myofasciitis | Loeys-Dietz Syndrome | Hypertensive Retinopathy | Atelosteogenesis Type 1 | Pouchitis | Hoyeraal-Hreidarsson Syndrome | Leukoplakia | Smoldering Myeloma | Colitis, Collagenous | Lung Diseases | Batten Disease | Familial Retinal Arterial Macroaneurysm | Polydactyly | Atopy | Postpartum Depression | Endometriosis | Myoclonus | Wolfram Syndrome 2 | Autoimmune Disease | Osteoporosis | Carcinoma In Situ | Vitamin B12 Deficiency | Sarcoidosis | Branchiootorenal Syndrome | Nephrotic Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Corneal Ulcer | Botulism | Myelofibrosis | Cerebrovascular Disorders | Patent Ductus Arteriosus | Osteopetrosis | Central Retinal Artery Occlusion | Relapsing Polychondritis | Primary Aldosteronism | Jalili Syndrome | Conjunctivitis, Allergic | Ocular Surface Squamous Neoplasia | Guillain-Barre Syndrome | Cramp Fasciculation Syndrome | X-linked Sideroblastic Anemia | Osteogenesis Imperfecta Type II | Albinism | Chronic Periodontitis | Astigmatism | Esotropia | Optic Atrophy 2 | Hypodontia | Dystrophy, Cone-rod | Astrocytoma, Anaplastic | Neural Tube Defect | Waardenburg Syndrome Type 2E | Hemolytic Uremic Syndrome, Atypical | Spinocerebellar Ataxia Type 42 | Agoraphobia | Dent Disease | Iron Deficiency Anemia | Iron Metabolism Disorders | Peripheral Neuropathy | Toxic Epidermal Necrolysis | Chylomicron Retention Disease | Guanidinoacetate Methyltransferase Deficiency | Chronic Thromboembolic Pulmonary Hypertension | Early Infantile Epileptic Encephalopathy 1 | Gangliosidosis | McLeod Syndrome | Poikiloderma With Neutropenia | Neovascular Glaucoma | Spinocerebellar Ataxia Type 40 | Anorexia Nervosa | Adenocarcinoma | Ataxia-ocular Apraxia 2 | Anemia | Adenylosuccinate Lyase Deficiency | Nephrocalcinosis | Bartsocas-Papas Syndrome | Skin Papilloma | Antithrombin III Deficiency | Ischemia | Eczema | Esthesioneuroblastoma | Pemphigus | Chordoid Glioma | Wagner Disease | Retinoblastoma | Familial Male-limited Precocious Puberty | Fraser Syndrome | Schindler Disease | Hypercholesterolemia | Methemoglobinemia | Myotonia | Keratitis-ichthyosis-deafness Syndrome | Peroxisomal Disorder | Rheumatic Heart Disease | Photosensitivity | Sarcoma | Danon Disease | Pure Autonomic Failure | Myocardial Infarction | 3C Syndrome | Chronic Lymphocytic Leukemia | Lymphedema | Wolcott-Rallison Syndrome | Saethre-Chotzen Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Congenital Hereditary Endothelial Dystrophy Type II | Dengue Hemorrhagic Fever | Meningococcal Meningitis | Abetalipoproteinemia | Glycogen Storage Disease Type 0, Muscle | AIDS | Wolfram Syndrome | Liver Failure | Carcinoma, Transitional Cell | Tendinopathy | Epidermolysis Bullosa Dystrophica | Scapuloperoneal Myopathy, X-linked Dominant | Nutrition Disorders | Sickle Cell Anemia | Enhanced S-cone Syndrome | Klippel-Feil Syndrome | Ligneous Conjunctivitis | Schwannomatosis | Olmsted Syndrome | Hepatitis | Pulmonary Sclerosing Hemangioma | Epidermolysis Bullosa Acquisita | Benign Familial Neonatal Convulsions | Schizophrenia | Brooke-Spiegler Syndrome | Hepatic Steatosis | Myelomeningocele | Osteoglophonic Dysplasia | Dyslipidemia | Cone Dystrophy | DEND Syndrome | Dyskeratosis Congenita | Interstitial Lung Diseases | Renal Hypouricemia | Robinow Syndrome | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | B-cell Chronic Lymphocytic Leukemia | Dyggve-Melchior-Clausen Disease | Hydrolethalus Syndrome | Chronic Myeloid Leukemia | Hereditary Neuropathy With Liability To Pressure Palsies | Sick Sinus Syndrome 1 | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Ureteropelvic Junction Obstruction | Galloway-Mowat Syndrome | Thyroid Dyshormonogenesis | Avian Influenza | Congenital Sodium Diarrhea | CHOPS Syndrome | Hemoglobinopathies | Spinocerebellar Ataxia Type 7 | Trichorhinophalangeal Syndrome | Pantothenate Kinase-associated Neurodegeneration | Pseudoexfoliation Syndrome | CEDNIK Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Antenatal Bartter Syndrome Type 1 | Lysosomal Acid Lipase Deficiency | Eccrine Porocarcinoma | Opisthorchiasis | Overactive Bladder | Argininosuccinic Aciduria | Onchocerciasis | Malignant Peripheral Nerve Sheath Tumor | Chondrodysplasia Punctata 1, X-linked Recessive | Leukocyte Adhesion Deficiency Type 1 | Neuropathy | Malignant Fibrous Histiocytoma | Chronic Myelomonocytic Leukemia | Shwachman-Bodian-Diamond Syndrome | Prolidase Deficiency | Liddle Syndrome | Bone Marrow Necrosis | Esophageal Motility Disorders