Disease

Strabismus

About the Disease
Mechanical Strabismus, also known as strabismus, is related to exophthalmos and graves disease 1, and has symptoms including ophthalmoplegia, spasm of conjugate gaze and anomalies of divergence. An important gene associated with Mechanical Strabismus is TPO (Thyroid Peroxidase), and among its related pathways/superpathways is Thyroxine (thyroid hormone) production. The drugs Propofol and Fentanyl have been mentioned in the context of this disorder. Affiliated tissues include eye, thyroid and brain.

Common Targets
G3479 | ACHE | HOXB1 | PAX6 | Nicotinic alpha1beta1deltaepsilon Receptor

疾病靶点研报
Strabismus

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

Other Diseases

Leukemia | Epidermolysis Bullosa Simplex | Protein S Deficiency | Pemphigus Foliaceus | MELAS Syndrome | Primary Hyperoxaluria Type 3 | Pheochromocytoma | Autonomic Nervous System Disorders | Epidermolysis Bullosa Dystrophica | Diabetes Type 2 | Gliosarcoma | Charcot-Marie-Tooth Disease, Type 1A | Neutropenia | Narcolepsy | Sarcoidosis | Intermittent Claudication | Gyrate Atrophy Of The Choroid And Retina | Infantile Neuroaxonal Dystrophy | Charcot-Marie-Tooth Disease Type 4B1 | Poirier-Bienvenu Neurodevelopmental Syndrome | Premature Ejaculation | Fibrosarcoma | Leiomyoma | Heterotopic Ossification | Frank-ter Haar Syndrome | Pleomorphic Xanthoastrocytoma | Microcephaly | Oral Lichen Planus | Leiomyosarcoma | Congenital Nephrotic Syndrome | Hyperhomocysteinemia | Alopecia | Non-epidermolytic Palmoplantar Keratoderma | Mitochondrial Disease | Woodhouse-Sakati Syndrome | Esotropia | KBG Syndrome | Chromosome 17q21.31 Deletion Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Shwachman-Bodian-Diamond Syndrome | Congestive Heart Failure | Varices | Myocarditis | Melanoma, Uveal | Primary Erythromelalgia | CREST Syndrome | Deafness, Dystonia, And Cerebral Hypomyelination | Pneumoconiosis | Okihiro Syndrome | Canavan Disease | Rhizomelic Chondrodysplasia Punctata | Intracranial Hypertension | Diabetic Neuropathy | Cat Eye Syndrome | Necrotizing Autoimmune Myopathy | Vertebrobasilar Insufficiency | Mucolipidosis Type III | Pneumonia, Bacterial | Tetanus | C3 Glomerulopathy | Spermatocele | Spinal Muscular Atrophy Type 2 | Dysequilibrium Syndrome | Agammaglobulinemia | Prolidase Deficiency | Acral Lentiginous Melanoma | Tinea Versicolor | Ameloblastic Carcinoma | Takotsubo Cardiomyopathy | Schindler Disease | LMNA-related Congenital Muscular Dystrophy | Brachial Plexus Neuropathy | Methemoglobinemia | Amish Infantile Epilepsy Syndrome | Giant Cell Arteritis | Cerebrotendinous Xanthomatosis | Adenylosuccinate Lyase Deficiency | Progressive Encephalopathy-optic Atrophy Syndrome | Retinal Coloboma | Diabetes Gestational | Myofibrillar Myopathy | Connective Tissue Disorders | Retinal Dystrophy, Early-onset Severe | Fetal And Neonatal Alloimmune Thrombocytopenia | Nager Acrofacial Dysostosis | Follicular Dendritic Cell Sarcoma | Crouzon Syndrome With Acanthosis Nigricans | Huntington's Disease | Ghosal Syndrome | Rheumatic Heart Disease | Blastoma, Pleuropulmonary | Loeys-Dietz Syndrome | Mountain Sickness | Chronic Granulomatous Disease | Tremor | Endometriosis | Sleep Apnea | Lipid Storage Diseases | Hepatitis B, Chronic | Pachyonychia Congenita | Hyperandrogenemia | Epicondylitis | Spondylo-ocular Syndrome | Adenomyosis | Neovascular Glaucoma | Polycystic Ovary Syndrome | Ophthalmia, Sympathetic | Paraganglioma, Carotid Body | Snyder-Robinson Syndrome | Cerebral Amyloid Angiopathy | Hamartoma | Superficial Spreading Melanoma | Pseudohypoaldosteronism | Hyperparathyroidism, Primary | X-linked Myotubular Myopathy | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Osmotic Demyelination Syndrome | Hypoparathyroidism | Achromatopsia | Muscle Wasting | Neurotoxicity | Aicardi-Goutieres Syndrome | Lung Diseases | Hyperparathyroidism-jaw Tumor Syndrome | Antiphospholipid Syndrome | Lichen Planus | Thrombasthenia | Congenital Adrenal Hyperplasia 1 | Pulmonary Vein Stenosis | Neurocutaneous Melanocytosis | Traboulsi Syndrome | Holoprosencephaly | Reticular Dysgenesis | Basal Ganglia Cerebrovascular Disease | Hypoplastic Left Heart Syndrome | Usher Syndrome Type II | Leukocyte Adhesion Deficiency Type 1 | Ischemia | Ureteropelvic Junction Obstruction | Ocular Albinism Type 1 | Multiple System Atrophy | Oligoasthenoteratozoospermia | Dyslipidemia | Skin Carcinoma | Pseudomyxoma Peritonei | Essential Fructosuria | Gastritis | Cerebrovascular Disorders | Mucormycosis | Myositis | Coffin-Lowry Syndrome | Scoliosis | Cavitary Optic Disc Anomalies | Schistosomiasis Mansoni | Pernicious Anemia | 5-oxoprolinase Deficiency | Fraser Syndrome | Transthyretin-related Amyloidosis | Antithrombin III Deficiency | Carcinoma, Transitional Cell | MIRAGE Syndrome | Crigler-Najjar Syndrome | Pyelonephritis | Renal Dysplasia | Alkaptonuria | Fabry's Disease | Tardive Dyskinesia | Myocardial Infarction | Benign Familial Neonatal Convulsions | Growth Hormone Excess | Primary Cutaneous Amyloidosis | Congenital Central Hypoventilation Syndrome | Trichorhinophalangeal Syndrome | Neuroendocrine Cancer | Hoyeraal-Hreidarsson Syndrome | Vici Syndrome | Spinocerebellar Ataxia Type 31 | Cancer, Brain | Hyperparathyroidism | Hereditary Sensory And Autonomic Neuropathy | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Glioblastoma Multiforme | Paroxysmal Nocturnal Hemoglobinuria | Carcinoma, Merkel Cell | Familial Thoracic Aortic Aneurysm | Guttate Psoriasis | Gigantism | 3C Syndrome | Progressive Myoclonic Epilepsy | Polyarteritis Nodosa | Combined Deficiency Of Factor V And Factor VIII | Endocarditis | Glomerulonephritis | Lupus Erythematosus | Duane Retraction Syndrome | Molybdenum Cofactor Deficiency | Tricho-hepato-enteric Syndrome | Cystitis | Cholestasis, Intrahepatic | Hypotrichosis Simplex | Peters-plus Syndrome | Desbuquois Syndrome | Progressive Familial Intrahepatic Cholestasis | Glycogen Storage Disease Type 9 | Li-Fraumeni Syndrome | Arts Syndrome | Leber Congenital Amaurosis | Fahr Disease | Carcinoma, Small Cell | Nance-Horan Syndrome | Primary Torsion Dystonia | Weill-Marchesani Syndrome | Vaginitis | Hyperinsulinemia | Esophageal Carcinoma | Cluster Headache | Cutaneous Angiosarcoma | Angelman Syndrome | Pantothenate Kinase-associated Neurodegeneration | Hyperinsulinemic Hypoglycemia | Torticollis | Neurofibroma, Plexiform | Seasonal Mood Disorder | Discoid Lupus Erythematosus | Wolcott-Rallison Syndrome | Intestinal Tuberculosis | Chediak-Higashi Syndrome | Polyradiculopathy | Nephrotic Syndrome Type 1 | Bladder Exstrophy | Retinal Dystrophy | T-cell Prolymphocytic Leukemia | Nephrosclerosis | Hemophagocytic Lymphohistiocytosis | Hyperthyroidism | Porphyria | Kabuki Syndrome 2 | Sorsby Fundus Dystrophy | Episodic Ataxia Type 2 | Charcot-Marie-Tooth Disease Type 4D | Multifocal Motor Neuropathy | Sclerosteosis | Still Disease | Adenosine Deaminase 2 Deficiency | Tyrosinemia Type 2 | Leukocyte Adhesion Deficiency | Retinopathy, Diabetic | Acquired Partial Lipodystrophy | Granular Corneal Dystrophy | Polycythemia | Stuttering | Neurofibromatosis-Noonan Syndrome | Hepatitis C, Chronic | Optic Nerve Diseases | Orthostatic Intolerance | Liver Failure | Ichthyosis, X-linked | Pouchitis | Vertigo | Dupuytren Disease | Patent Foramen Ovale | Synpolydactyly | Recurrent Respiratory Papillomatosis | Blepharospasm | Atopic Dermatitis | Acrocallosal Syndrome | Ectrodactyly | Spinocerebellar Ataxia Type 13 | Optic Nerve Hypoplasia, Bilateral | Congenital Heart Block | Liebenberg Syndrome | Angina Pectoris | Apparent Mineralocorticoid Excess Syndrome | Tay-Sachs Disease | Stroke, Ischemic | Meleda Disease | Renal Tubular Dysgenesis | Cystinuria | Proximal Symphalangism | Delirium | Multiple Sclerosis, Secondary Progressive | Central Core Disease | Macular Corneal Dystrophy Type 1 | Cystinosis | DRESS Syndrome | Werner's Syndrome | Donnai-Barrow Syndrome | Dystonia Musculorum Deformans | Mitochondrial Cytopathy | Paroxysmal Kinesigenic Dyskinesia | Lymphedema | Trimethylaminuria | Porphyria, Acute Intermittent | Congenital Dyserythropoietic Anemia | Choroiditis | Schistosomiasis | Dysmorphophobia | Onchocerciasis | Posterior Polar Cataract | Vulvovaginitis | Tuberculosis | Smoldering Myeloma | Gastritis, Atrophic | H Syndrome | Priapism | Spinocerebellar Ataxia Type 15 | Acne | Myofibromatosis | Intermittent Explosive Disorder | Hyperbilirubinemia, Neonatal | Cystitis, Interstitial | Hyperacusis | Intestinal Pseudo-obstruction | Oguchi Disease-2 | Vitamin A Deficiency | Pulmonary Veno-occlusive Disease | Tendinopathy | Coffin-Siris Syndrome | Gerodermia Osteodysplastica | Anovulation | Toxic Epidermal Necrolysis | Chronic Mucocutaneous Candidiasis | Spinocerebellar Ataxia Type 42 | Hartnup Disease | Antenatal Bartter Syndrome Type 1 | Fuchs Dystrophy | Ichthyosis | Polyneuropathy | Proctitis | Papillorenal Syndrome | Familial Pheochromocytoma-paraganglioma | GM2-gangliosidosis AB Variant | Uremia | Lissencephaly 2 | Aspartylglycosaminuria | Malaria | Osteochondroma | Nephrotic Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Long QT Syndrome Type 2 | Creatine Deficiency Syndrome Due To AGAT Deficiency | Persistent Hyperplastic Primary Vitreous | Pendred Syndrome | Niemann-Pick Disease | Congenital Dyserythropoietic Anemia Type 1 | Thymoma, Malignant | Meesmann Corneal Dystrophy | Cryptococcal Meningitis | Gitelman Syndrome | Retinitis Pigmentosa | Pneumococcal Meningitis | Imerslund-Grasbeck Syndrome | Osteoarthritis | Retinitis | Sturge-Weber Syndrome | Hypohidrotic Ectodermal Dysplasia | Neurofibromatosis | Congenital Stationary Night Blindness | Spinocerebellar Ataxia Type 12 | Succinic Semialdehyde Dehydrogenase Deficiency | Mucolipidosis | Benign Familial Pemphigus | Keloid | High Molecular Weight Kininogen Deficiency | Autosomal Recessive Congenital Ichthyosis | Atrioventricular Septal Defect | Amyotrophic Lateral Sclerosis | Hyperkalemic Periodic Paralysis | Wagner Disease | Behavioral Variant Of Frontotemporal Dementia | Globozoospermia | Dermatitis Herpetiformis | Pericarditis | Sleep Apnea, Central | Familial Dysautonomia | Heart Failure | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Neurofibrosarcoma | Neuroectodermal Tumors, Primitive | Kaposi Sarcoma | Autosomal Recessive Bestrophinopathy | Dubin-Johnson Syndrome | Nestor-Guillermo Progeria Syndrome | Agoraphobia | Cryptorchidism | Spondyloepiphyseal Dysplasia Tarda, X-linked | Hypermetropia | Herpes Genitalis | Usher Syndrome Type I | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Schnitzler Syndrome | Eczema | Encephalitis | Juvenile Hyaline Fibromatosis | Multiple Sclerosis, Chronic Progressive | Cartilage Disorders | Malonyl-CoA Decarboxylase Deficiency | Huntington's Disease-like 2 | Erythromelalgia | Macrophage Activation Syndrome