Disease

Chitayat Syndrome

About the Disease
Chitayat Syndrome, also known as chyts, is related to roifman-chitayat syndrome and stalker chitayat syndrome. An important gene associated with Chitayat Syndrome is ERF (ETS2 Repressor Factor). The drugs Bethanechol and Acetylcysteine have been mentioned in the context of this disorder. Affiliated tissues include lung, trachea and respiratory system-trachea, and related phenotypes are generalized hypotonia and delayed speech and language development

Common Targets
ERF | ETF1

疾病靶点研报
Chitayat Syndrome

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

Other Diseases

Long QT Syndrome Type 2 | Blepharitis | Charcot-Marie-Tooth Disease, Type 2 | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Demyelinating Diseases | Oligospermia | Acute Leukemia | Uveitis | Glycogen Storage Disease Type 1b | Blastomycosis | Thyrotoxic Periodic Paralysis | Myoclonic Atonic Epilepsy | Sertoli Cell-only Syndrome | Apraxia | Overactive Bladder | Haim-Munk Syndrome | Chordoid Glioma | Triple A Syndrome | Glioma | Generalized Epilepsy And Paroxysmal Dyskinesia | Fibromuscular Dysplasia | Antenatal Bartter Syndrome Type 1 | Dystonia | Irritable Bowel Syndrome | Spastic Paraplegia Type 7 | Erythromelalgia | Tangier Disease | Adult Polyglucosan Body Disease | Diabetic Nephropathy | Keratoconus | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | VACTERL Association | Congenital Stromal Corneal Dystrophy | Hydrocephalus | Deafness, Dystonia, And Cerebral Hypomyelination | Megaloblastic Anemia | Subacute Sclerosing Panencephalitis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Usher Syndrome Type I | Larsen Syndrome | Acne | Greenberg Dysplasia | Hypercholesterolemia, Familial | Congenital Dysfibrinogenemia | Spinocerebellar Ataxia Type 10 | Familial Advanced Sleep Phase Syndrome | Anemia | Polycystic Kidney, Autosomal Recessive | Prediabetes | Hypertensive Retinopathy | Spinocerebellar Ataxia Type 27 | KBG Syndrome | Myoclonus-dystonia Syndrome | Bloom Syndrome | CEDNIK Syndrome | Chronic Inflammatory Demyelinating Polyneuropathy | Situs Inversus | Teratozoospermia | Heroin Dependence | Mitochondrial DNA Depletion Syndrome 13 | TARP Syndrome | Acromicric Dysplasia | Multiple Sclerosis | Hennekam Lymphangiectasia-lymphedema Syndrome | Plasma Cell Dyscrasia | Eiken Syndrome | Epidermolytic Ichthyosis, Annular | Greig Cephalopolysyndactyly Syndrome | Polycystic Liver | Thrombocytopenia | Bruck Syndrome | Familial Pheochromocytoma-paraganglioma | Precocious Puberty | Infantile Spasm | Vertigo | Carcinoma, Merkel Cell | Metachromatic Leukodystrophy | Disseminated Superficial Actinic Porokeratosis | Myofibromatosis | Congenital Lipoid Adrenal Hyperplasia | Charcot-Marie-Tooth Disease Type 2E | Fascioliasis | Phosphoglycerate Dehydrogenase Deficiency | Dwarfism | Leukemia-lymphoma, Adult T-cell | Incontinentia Pigmenti | Diabetic Macular Edema | Autism | Erythema Multiforme | Melanoma, Uveal | Pulmonary Stenosis | Alkaptonuria | Polycythemia Vera | Pycnodysostosis | Retinal Dystrophy, Early-onset Severe | GATA2 Deficiency | Seasonal Mood Disorder | Kernicterus | Treacher Collins Syndrome | Tinea Versicolor | Carbamoyl Phosphate Synthetase I Deficiency | Lesch-Nyhan Syndrome | Tremor | Endophthalmitis | Trichothiodystrophy | Meconium Ileus | Adenomatoid Tumor | Waardenburg Syndrome Type 4 | Chondrosarcoma | Acute Chest Syndrome | Glutaric Aciduria Type 1 | Retinopathy Of Prematurity | Whipple's Disease | Primary Hyperoxaluria | Hemolytic Anemia | Pulmonary Veno-occlusive Disease | Thrombophilia | Angioedema, Hereditary | Giant Cell Glioblastoma | Ectrodactyly | Duane Retraction Syndrome | Woodhouse-Sakati Syndrome | Peutz-Jeghers Syndrome | Asthma, Exercise-induced | Kabuki Syndrome | Hyperlipidemia, Familial Combined | Sialoadenitis | Hereditary Spastic Paraplegia | Autonomic Neuropathy | Congenital Ichthyosiform Erythroderma | Familial Episodic Pain Syndrome | Porphyria, Variegate | Vitamin K Deficiency | Large Granular Lymphocytic Leukemia | Dysthymia | Seizures-scoliosis-macrocephaly Syndrome | Neurodevelopmental Disorders | Gaucher Disease | Basal Ganglia Disease | Renal Failure | Orthostatic Intolerance | Congenital Heart Block | Retinitis Pigmentosa | Cirrhosis | Nephroblastoma | Dental Caries | Sporadic Inclusion Body Myositis | Sarcomatoid Carcinoma Of The Lung | Neurofibroma, Plexiform | Follicular Dendritic Cell Sarcoma | Chronic Enteropathy Associated With SLCO2A1 Gene | Chondroma | Craniosynostosis | Peritonitis | Thyroid Dyshormonogenesis | Pseudohypoparathyroidism Type 1C | Osteopetrosis | Hereditary Mixed Polyposis Syndrome | Benign Familial Infantile Seizures | Tibial Muscular Dystrophy | Cryptococcal Meningitis | Progressive Familial Intrahepatic Cholestasis | Myasthenia Gravis | Wolman Disease | Ganglioneuroma | Keratopathy | Corneal Neovascularization | Osteogenesis Imperfecta Type I | Otitis Externa | Acrodermatitis | Acute Generalized Exanthematous Pustulosis | Reye Syndrome | Glutaric Aciduria Type 3 | Vitiligo | Glaucoma, Congenital | Still Disease | Hypertension, Pulmonary | Aldosteronism | Schindler Disease | Chitayat Syndrome | Globozoospermia | Oligoasthenoteratozoospermia | Leri Pleonosteosis | Heart Failure | Hereditary Sensory Neuropathy Type 1 | Hereditary Hemorrhagic Telangiectasia Type 2 | Priapism | NDH Syndrome | Nance-Horan Syndrome | Cardiomyopathy, Dilated, 1L | Choriocarcinoma | Carbohydrate Metabolism Disorders | Polymyositis | Oguchi Disease-2 | Pneumothorax | Pseudo-pseudohypoparathyroidism | Blepharoconjunctivitis | Sleep Disorder | Histiocytosis | Cleidocranial Dysplasia | Heavy Chain Disease | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Chromosome 17q21.31 Deletion Syndrome | Meesmann Corneal Dystrophy | Connective Tissue Disorders | Epidermolysis Bullosa Acquisita | Tylosis With Esophageal Cancer | Fowler's Syndrome | Lipodystrophy | Discoid Lupus Erythematosus | Lymphoma, AIDS-related | Strabismus | Epilepsy Of Infancy With Migrating Focal Seizures | Congenital Dyserythropoietic Anemia Type 4 | Spondyloepiphyseal Dysplasia Tarda, X-linked | Tietze Syndrome | Nasodigitoacoustic Syndrome | Exostoses | Bardet-Biedl Syndrome | Portal Vein Thrombosis | Macrodactyly | Cervicitis | Uterine Leiomyoma | Richter's Syndrome | Thrombasthenia | Corneal Ulcer | Inflammatory Myopathy | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Autoimmune Disease | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Acute Lymphocytic Leukemia | Ichthyosis Bullosa Of Siemens | Crimean-Congo Hemorrhagic Fever | Adenomyosis | Ehlers-Danlos Syndrome | Ectodermal Dysplasia | Spina Bifida | Addison Disease | Hypothyroidism | Asthma, Nocturnal | Spinocerebellar Ataxia Type 13 | Xeroderma Pigmentosum Variant Type | Diarrhea | Hepatic Steatosis | Acute Tubular Necrosis | Glioblastoma Multiforme | Cushing Syndrome | Bipolar Disorder | Parkinsonism | Usher Syndrome Type IIC | Jaundice, Obstructive | Epidermolysis Bullosa Simplex, Generalized | Hypogammaglobulinemia | Plasma Cell Leukemia | Keratitis | Pneumonia, Bacterial | Osteosarcoma | Cancer, Breast | Paget's Disease Of The Breast | Dyggve-Melchior-Clausen Disease | Major Depression | Spondylocostal Dysostosis | Enlarged Vestibular Aqueduct | Mevalonate Kinase Deficiency | Inflammatory Joint Disease | Lathosterolosis | Albinism | Erysipelas | Lentigo | Coronary Artery Disease | Lymphedema-distichiasis Syndrome | Microvillus Inclusion Disease | Triphalangeal Thumb-polysyndactyly Syndrome | Pupil Disorders | Thyroiditis | GLUT1 Deficiency Syndrome | Blood Protein Disorders | Tay-Sachs Disease | Familial Mediterranean Fever | Glanzmann Thrombasthenia | Mitochondrial DNA Depletion Syndrome | Brenner Tumor | Geleophysic Dysplasia | Echinococcosis | Parkinson Disease 6, Autosomal Recessive Early-onset | Botulism | Waardenburg Syndrome Type 1 | Anencephaly | Paraganglioma, Carotid Body | Low Tension Glaucoma | Metaphyseal Chondrodysplasia, Schmid Type | Odonto-onycho-dermal Dysplasia | Liver Diseases | Anovulation | Multiple Hamartoma Syndrome | Onchocerciasis | Juvenile Myelomonocytic Leukemia | Myofibrillar Myopathy | Hereditary Inclusion Body Myopathy | Hemosiderosis | Johanson-Blizzard Syndrome | Olmsted Syndrome | Aarskog-Scott Syndrome | Charcot-Marie-Tooth Disease Type 4 | HIBCH Deficiency | Amebiasis | Tyrosinemia Type 1 | Cerebellofaciodental Syndrome | Amelogenesis Imperfecta | Anterior Segment Dysgenesis | Acute Coronary Syndrome | Bartter Syndrome | Spinocerebellar Ataxia Type 38 | Bietti Crystalline Dystrophy | Cluster Headache | Pilomatrix Carcinoma | Keratosis, Actinic | Angiosarcoma Of The Breast | Inflammatory Bowel Disease | Choroideremia | Coma | Potocki-Shaffer Syndrome | Moyamoya Disease | Congenital Adrenal Hyperplasia | Erectile Dysfunction | Trichotillomania | Restrictive Dermopathy | Multisystemic Smooth Muscle Dysfunction Syndrome | Infantile Nephropathic Cystinosis | Aneurysm, Thoracic Aortic | Spinocerebellar Ataxia Type 28 | Diabetes | Alcoholism | Sclerosteosis 2 | Galactosemia | Glomerulonephritis | Sengers Syndrome | Cardiomyopathy, Restrictive | Rhabdomyosarcoma, Alveolar | Kawasaki Disease | Pontocerebellar Hypoplasia | Nemaline Myopathy | Distal Spinal Muscular Atrophy | Pheochromocytoma | Macular Degeneration | Hepatic Adenomatosis | Hypotrichosis Simplex | Skin Papilloma | Rift Valley Fever | Milk Allergy | Pseudoexfoliation Syndrome | Cutaneous Angiosarcoma | Primary Hyperoxaluria Type 3 | Dermatomyositis | Influenza | Charcot-Marie-Tooth Disease Type 2T | Erythropoietic Protoporphyria | Contact Dermatitis | Dysgerminoma | Progressive External Ophthalmoplegia | SAPHO Syndrome | Rash | Urethritis | Myopathy | Salla Disease | Menkes Disease | Conduct Disorder | Cartilage Disorders | GNE Myopathy | Inflammatory Myofibroblastic Tumor | Lattice Corneal Dystrophy | Microphthalmia | Pineoblastoma | Hemophilia | Hydrops Fetalis | Wagner Disease | Yellow Fever | Benign Hereditary Chorea | Small Lymphocytic Lymphoma | Hypercalcemia | Combined Deficiency Of Factor V And Factor VIII | Fuchs Heterochromic Iridocyclitis | Granular Corneal Dystrophy | Autosomal Recessive Congenital Ichthyosis | Meningeal Melanocytoma | Hemochromatosis Type 2 | Vertebrobasilar Insufficiency | Multicentric Carpotarsal Osteolysis Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Immunoproliferative Disorders | Parkinson's Disease | Scleritis | Niemann-Pick Disease, Type B | Left Ventricular Noncompaction | Meier-Gorlin Syndrome | Hereditary Sensory And Autonomic Neuropathy | Hyperthermia, Malignant | Niemann-Pick Disease, Type A | Schizoaffective Disorder