Usher Syndrome Type III

About the Disease
Usher Syndrome, Type Iiia, also known as usher syndrome type 3, is related to usher syndrome, type ij and usher syndrome, type if. An important gene associated with Usher Syndrome, Type Iiia is CLRN1 (Clarin 1), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include eye, retina and brain, and related phenotypes are sensorineural hearing impairment and abnormal electroretinogram

Common Targets
ID1 | RGS7 | ABHD12 | HSPD1 | ADGRV1 | USH2A | CLRN1

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

Other Diseases

Sleep Apnea, Central | Trichorhinophalangeal Syndrome | Rhabdomyosarcoma, Alveolar | Mandibuloacral Dysplasia With Type A Lipodystrophy | Toxoplasmosis | Congenital Disorders Of Glycosylation Type II | Craniometaphyseal Dysplasia | Purpura, Thrombotic Thrombocytopenic | Unverricht-Lundborg Syndrome | Pseudohypoaldosteronism | Infectious Diarrhea | Arthritis, Gouty | Colitis, Microscopic | Cockayne Syndrome | Mucormycosis | Congenital Tufting Enteropathy | Non-small Cell Lung Cancer | Achondrogenesis | Lysosomal Acid Lipase Deficiency | Sclerosteosis | Cri-du-chat Syndrome | Glanzmann Thrombasthenia | Yellow Fever | Sturge-Weber Syndrome | Eczema | Corneal Neovascularization | Congenital Dyserythropoietic Anemia Type 1 | Pemphigus Vulgaris | Charcot-Marie-Tooth Disease Type 4B1 | Mohr-Tranebjaerg Syndrome | Cysticercosis | Pure Autonomic Failure | Charcot-Marie-Tooth Disease Type 4E | Charcot-Marie-Tooth Disease, Type 2C | Hamartoma | X-linked Myotubular Myopathy | Leber Hereditary Optic Neuropathy | Urticaria | Personality Disorders | Polycystic Kidney, Autosomal Dominant | Epidermolytic Hyperkeratosis | Hyperlipidemia, Familial Combined | B-cell Prolymphocytic Leukemia | Brugada Syndrome 1 | Pituitary Disorders | Non-Hodgkin Lymphoma | Spinocerebellar Ataxia Type 23 | Persistent Hyperplastic Primary Vitreous | Pulmonary Stenosis | Chorea-acanthocytosis | Neurocutaneous Syndromes | Hepatoblastoma | Dengue Hemorrhagic Fever | Acromicric Dysplasia | Hyperlipidemia Type V | Rickets | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Lichen Sclerosus | Limb Girdle Muscular Dystrophy | Metaphyseal Chondrodysplasia, Schmid Type | Hartsfield Syndrome | Cancer, Kidney | Ataxia-ocular Apraxia 2 | Spinocerebellar Ataxia Type 10 | Inflammatory Myopathy | Neuropathy | Raine Syndrome | Aicardi-Goutieres Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Depression | Oral Lichen Planus | Mountain Sickness | Autonomic Neuropathy | Spitz Nevus | Barakat Syndrome | Anencephaly | Hepatic Steatosis | Glioblastoma Multiforme | Hereditary Folate Malabsorption | Essential Fructosuria | Epithelioid Hemangioma | Familial Hypertrophic Cardiomyopathy | Lyme Disease | Stuve-Wiedemann Syndrome | Thrombocytopenia | Dysmorphophobia | Dowling-Degos Disease | Pemphigus Foliaceus | Dyslexia | Retinitis Pigmentosa | Porphyria, Variegate | HUPRA Syndrome | Cholesteryl Ester Storage Disease | Arthropathy | Panic Disorder | Saethre-Chotzen Syndrome | Hartnup Disease | Myosin Storage Myopathy | Amebiasis | Compartment Syndrome | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Fahr Disease | Graft-versus-host Disease | Proteus Syndrome | Okihiro Syndrome | Crimean-Congo Hemorrhagic Fever | Charcot-Marie-Tooth Disease Type 2D | Central Pain Syndrome | Cranioectodermal Dysplasia | Acne Vulgaris | Roberts Syndrome | Empyema | Coronary Restenosis | Congenital Myasthenic Syndrome | Schizencephaly | Meconium Ileus | 3-methylglutaconic Aciduria Type IV | 3-methylglutaconic Aciduria | Oculopharyngeal Muscular Dystrophy | Mitochondrial Cytopathy | Plasma Cell Dyscrasia | Ureteropelvic Junction Obstruction | Glutaric Aciduria Type 1 | Pineoblastoma | Neurofibrosarcoma | Nicotine Addiction | Long QT Syndrome Type 1 | Primary Pigmented Nodular Adrenocortical Disease | Primary Erythromelalgia | Hepatitis, Alcoholic | IgA Nephropathy | Sarcoma, Alveolar Soft Part | Craniofrontonasal Syndrome | Amenorrhea | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Hepatopulmonary Syndrome | Cardiomyopathy, Dilated, 1L | Left Ventricular Noncompaction | Endometritis | Infantile Liver Failure Syndrome 1 | Idiopathic Multicentric Castleman Disease | Meleda Disease | Hyperhomocysteinemia | Hydronephrosis | Krabbe Disease | HELLP Syndrome | Infertility | Gastroenteritis, Eosinophilic | Lipid Storage Myopathy | Diabetes Insipidus | Metachondromatosis | Congenital Heart Block | Waardenburg Syndrome Type 2E | Schindler Disease | Postpartum Depression | Cerebellar Ataxia, Cayman Type | Epidermolysis Bullosa | Myelofibrosis | Stiff-man Syndrome | Vitreoretinopathy, Proliferative | Intermittent Explosive Disorder | Rash | Fascioliasis | Arrhythmogenic Right Ventricular Cardiomyopathy | Primary Familial Brain Calcification | Cramp Fasciculation Syndrome | CHARGE Syndrome | Multiple Sclerosis, Secondary Progressive | Premature Ejaculation | Osmotic Demyelination Syndrome | Xeroderma Pigmentosum Variant Type | Congenital Sodium Diarrhea | Muckle-Wells Syndrome | Juvenile Myelomonocytic Leukemia | Peters-plus Syndrome | Hyperferritinemia-cataract Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Spondylocostal Dysostosis | Ovarian Sex Cord-stromal Tumor | Sleep Apnea | Heavy Chain Disease | Apparent Mineralocorticoid Excess Syndrome | Osteopathia Striata With Cranial Sclerosis | Abetalipoproteinemia | Infantile Spasm | Esophageal Motility Disorders | Sengers Syndrome | Osteogenesis Imperfecta | Congenital Stromal Corneal Dystrophy | Tuberculous Meningitis | Smith-Magenis Syndrome | Malignant Peripheral Nerve Sheath Tumor | Prostatitis | Enlarged Vestibular Aqueduct | Cartilage Disorders | Keratosis, Seborrheic | Pseudohypoparathyroidism Type 1A | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Myoclonic Atonic Epilepsy | Renal Hypomagnesemia 3 | Hemophagocytic Lymphohistiocytosis | Craniofacial Dysostosis | Treacher Collins Syndrome | Acute Generalized Exanthematous Pustulosis | Dystrophy, Cone-rod | Glycogen Storage Disease Type 5 | Retinal Vasculitis | Pseudohypoparathyroidism Type 1B | Preaxial Polydactyly | Congenital Central Hypoventilation Syndrome | Osteosclerosis | Lymphangiomatosis | Polycystic Ovary Syndrome | Charcot-Marie-Tooth Disease | 3-M Syndrome | Postaxial Polydactyly | Mosaic Variegated Aneuploidy Syndrome 2 | Demyelinating Diseases | Diamond-Blackfan Anemia | Hoyeraal-Hreidarsson Syndrome | Malaria | Skin Carcinoma | Paraplegia | Androgenic Alopecia | Borderline Personality Disorder | Martsolf Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Steel Syndrome | Seminoma | Systemic Mastocytosis | Sezary Syndrome | Anterior Segment Dysgenesis | Chromosome 9q34.3 Deletion Syndrome | McLeod Syndrome | Marfan Syndrome | Multiple Myeloma | Mastitis | Retinal Detachment | Cholangiocarcinoma | Malaria, Cerebral | Reflex Epilepsy | Leigh Syndrome | Varicocele | Leukocyte Adhesion Deficiency | Aspergillosis | Pseudoexfoliation Syndrome | Becker Muscular Dystrophy | Motor Neuron Diseases | X-linked Sideroblastic Anemia | Vitiligo | Influenza | Eccrine Porocarcinoma | Myopia | Infertility, Male | Congenital Heart Defects | Myofibrillar Myopathy | Renal Medullary Carcinoma | Bronchitis | Myelitis, Transverse | Vertigo | Pregnancy, Ectopic | Gestational Trophoblastic Disease | Cerebellofaciodental Syndrome | Schistosomiasis | Sporadic Hemiplegic Migraine | Renal Dysplasia | Spinocerebellar Ataxia Type 12 | Joubert Syndrome | Pulverulent Zonular Cataract | Congenital Hereditary Endothelial Dystrophy Type II | Renal Failure | Primary Cutaneous Amyloidosis | Adenoma, Pleomorphic | Sertoli Cell-only Syndrome | Blepharoconjunctivitis | Gilbert Syndrome | Craniosynostosis | Hernia, Inguinal | Rosacea | Renal-hepatic-pancreatic Dysplasia | Pneumonia, Bacterial | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Dupuytren Disease | Antisynthetase Syndrome | Paget's Disease Of The Breast | Brenner Tumor | Binge Eating Disorder | Persistent Truncus Arteriosus | Guillain-Barre Syndrome | Opisthorchiasis | Lesch-Nyhan Syndrome | Waardenburg Syndrome | Asphyxia Neonatorum | Cheilitis | Cabezas Syndrome | Familial Thoracic Aortic Aneurysm | Pyloric Stenosis, Infantile Hypertrophic | Delirium | Achromatopsia | Arteriosclerosis | Gingivitis | Insulin Resistance | Carpal Tunnel Syndrome | Ichthyosis Bullosa Of Siemens | Osteogenesis Imperfecta Type VI | Histiocytic Sarcoma | Hypertension, Portal | Multiple Epiphyseal Dysplasia | Metachromatic Leukodystrophy | Shwachman-Bodian-Diamond Syndrome | Rhabdomyosarcoma, Embryonal | Paracoccidioidomycosis | Polycythemia | Poretti-Boltshauser Syndrome | Aplasia Cutis Congenita | Cholera | Heroin Dependence | Duodenal Atresia | Conjunctivitis | Cryopyrin-associated Periodic Syndromes | Scleritis | Donnai-Barrow Syndrome | Combined Deficiency Of Factor V And Factor VIII | Niemann-Pick Disease, Type A | Adrenoleukodystrophy, X-linked | Papillorenal Syndrome | Acute Kidney Injury | Alopecia Areata | Meniere's Disease | Communication Disorders | Scoliosis | Richter's Syndrome | Zollinger-Ellison Syndrome | Spinocerebellar Ataxia Type 1 | Familial Pheochromocytoma-paraganglioma | Dyskeratosis Congenita | Osteoporosis | Osteoporosis-pseudoglioma Syndrome | Multicystic Renal Dysplasia | Pancreatitis | Spinocerebellar Ataxia Type 13 | Porphyria | Smith-Kingsmore Syndrome | Erectile Dysfunction | Glaucoma | Liebenberg Syndrome | Camptocormia | Cholestasis, Intrahepatic | Spinocerebellar Ataxia Type 8 | Dengue Shock Syndrome | Prediabetes | Intermittent Claudication | Otopalatodigital Syndrome Type 2 | Palmoplantar Keratoderma | Ectrodactyly | Schistosomiasis Mansoni | Precocious Puberty | Gastritis | Blue Rubber Bleb Nevus Syndrome | Carey-Fineman-Ziter Syndrome | Hypospadias | Lupus Erythematosus | Vestibular Disease | Otitis Media | Congenital Muscular Dystrophy | Neuroectodermal Tumors, Primitive | Hypoglycemia | Nephritis, Interstitial | Spinocerebellar Ataxia Type 40 | Smoldering Myeloma | Albinism | Nasodigitoacoustic Syndrome | Keratopathy | Syndactyly | Galactosialidosis | Sialidosis | Wolman Disease | Agoraphobia | Hereditary Mixed Polyposis Syndrome | Autosomal Recessive Congenital Ichthyosis | Goldenhar Syndrome | Senior-Loken Syndrome | Hepatitis B, Chronic | Diverticulitis | Aarskog-Scott Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Asthma, Nocturnal | Carcinoma, Squamous Cell | Heimler Syndrome | Encephalopathy, Hepatic | Hypobetalipoproteinemias | Ellis-Van Creveld Syndrome | T-cell Prolymphocytic Leukemia | Avian Influenza | Mitochondrial Myopathy | Rubinstein-Taybi Syndrome | Thalassemia | Adult Polyglucosan Body Disease | Acromegaly | Cancer, Breast