Corneal Dystrophy And Perceptive Deafness

About the Disease
Corneal Dystrophy and Perceptive Deafness, also known as corneal dystrophy-perceptive deafness syndrome, is related to corneal dystrophy and corneal edema. An important gene associated with Corneal Dystrophy and Perceptive Deafness is SLC4A11 (Solute Carrier Family 4 Member 11), and among its related pathways/superpathways is Transport of inorganic cations/anions and amino acids/oligopeptides. Affiliated tissues include endothelial, eye and brain, and related phenotypes are corneal opacity and sensorineural hearing impairment

Common Targets
SLC4A11

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

Other Diseases

Stargardt Disease | Alopecia Totalis | Cystitis | Juvenile Xanthogranuloma | Hemangioma | Intracranial Hypertension | Hidradenitis Suppurativa | Situs Inversus | Huntington's Disease | Angiosarcoma | Constipation | Postpartum Depression | Sotos Syndrome | Dwarfism | Waardenburg Syndrome Type 2 | Pseudohermaphroditism | Centronuclear Myopathy | Anorchia | Hypercalcemia | Transcobalamin Deficiency | Perry Syndrome | Sarcoma, Endometrial Stromal | Pterygium | Sulfite Oxidase Deficiency | Chondrosarcoma | Hypoproteinemia, Hypercatabolic | Cardiomyopathy, Dilated, 1L | Thyroiditis | Okihiro Syndrome | Peyronie's Disease | Cancer, Lung | Reye Syndrome | Vascular Calcification | Chronic Neutrophilic Leukemia | Acute Chest Syndrome | Paget's Disease Of The Breast | Porphyria, Variegate | Ventricular Septal Defect | Usher Syndrome Type II | Spondylocarpotarsal Synostosis Syndrome | Spinocerebellar Ataxia Type 3 | Hyperbilirubinemia, Neonatal | Trichothiodystrophy | Urethritis | Neurofibromatosis Type 1 | Vitamin A Deficiency | Hyperandrogenemia | Oculopharyngeal Muscular Dystrophy | Neuronal Ceroid Lipofuscinosis | Beare-Stevenson Syndrome | Premenstrual Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Primary Progressive Aphasia | Glaucoma | Pseudoexfoliation Syndrome | Pelizaeus-Merzbacher Disease | Hyperammonemia | Congenital Aniridia | Central Pain Syndrome | Pulmonary Alveolar Proteinosis | Sialidosis | Hemorrhage | Scleroderma | Birt-Hogg-Dube Syndrome | Rothmund-Thomson Syndrome | Eclampsia | Angiomyolipoma | Malaria | Porokeratosis | Ureteropelvic Junction Obstruction | Progressive Myoclonic Epilepsy | Orotic Aciduria | Cancer, Bladder | Depression | Meningioma | Actinomycetoma | Portal Vein Thrombosis | Spinocerebellar Ataxia Type 16 | Scapuloperoneal Spinal Muscular Atrophy | GAPO Syndrome | Camurati-Engelmann Disease | Fowler's Syndrome | Tonsillitis | Personality Disorders | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Marinesco-Sjogren Syndrome | Poikiloderma With Neutropenia | FG Syndrome | Aplasia Cutis Congenita | Antiphospholipid Syndrome | Pituitary Disorders | Chondrodysplasia Punctata 2, X-linked Dominant | Budd-Chiari Syndrome | Acute Lymphocytic Leukemia | Joubert Syndrome | Cold-induced Sweating Syndrome | Hermansky-Pudlak Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Spondylocostal Dysostosis | Van Der Knaap Disease | Fascioliasis | Primary Hyperoxaluria | Periodontitis | Iron Metabolism Disorders | Adult Polyglucosan Body Disease | Glomerulonephritis | Chordoma | Arrhythmogenic Right Ventricular Cardiomyopathy | Optic Neuropathy | Dystonia Musculorum Deformans | Traboulsi Syndrome | Hemoglobinopathies | Trichorhinophalangeal Syndrome | Trigonocephaly | Lesch-Nyhan Syndrome | Tic Disorder | Specific Granule Deficiency | Ichthyosis Hystrix, Curth-Macklin Type | Heart Septal Defects | Pregnancy, Ectopic | Cancer, Breast | Familial Exudative Vitreoretinopathy | Turner's Syndrome | Glucagonoma | Agnathia-Otocephaly Complex | Cancer, Kidney | Fetal Akinesia Deformation Sequence | Gardner Syndrome | Fibromuscular Dysplasia | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Restrictive Dermopathy | Neurodermatitis | Neutrophilia | Arthritis, Reactive | Retinal Dystrophy | Multiple Sulfatase Deficiency | Sleep Apnea | Imerslund-Grasbeck Syndrome | Amyotrophic Lateral Sclerosis, Juvenile | Leri Pleonosteosis | Osmotic Demyelination Syndrome | Riboflavin Transporter Deficiency Neuronopathy | Cheilitis | Idiopathic Multicentric Castleman Disease | HELLP Syndrome | Autism | Multiple Sclerosis, Primary Progressive | Inflammatory Bowel Disease | Myoclonic Epilepsy With Ragged Red Fibers | Acrodermatitis Enteropathica | Hypertriglyceridemia | Benign Recurrent Intrahepatic Cholestasis 1 | Schindler Disease | Odonto-onycho-dermal Dysplasia | GATA2 Deficiency | Cardiomyopathy, Peripartum | Pierre Robin Syndrome | Osteosarcoma | Wagner Disease | Polyarteritis Nodosa | Liddle Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Supravalvular Aortic Stenosis | Encephalopathy | Anti-glomerular Basement Membrane Disease | Pilomatrix Carcinoma | Gastritis | Carpenter Syndrome | Bronchitis | Methemoglobinemia Type IV | Chronic Granulomatous Disease | Tibial Muscular Dystrophy | Pituitary Dwarfism | Liver Failure, Acute Infantile | Cholangiocarcinoma | Primary Lateral Sclerosis | Seborrheic Dermatitis | Aceruloplasminemia | Agammaglobulinemia | Myopia | Ganglioneuroma | Retinal Dystrophy, Early-onset Severe | Purpura, Thrombotic Thrombocytopenic | Retinopathy Of Prematurity | Dysmorphophobia | Thyroid Hormone Resistance | Ganglioglioma | Pulverulent Zonular Cataract | Kohlschutter-Tonz Syndrome | Lissencephaly 2 | Lymphoma, Follicular | Salla Disease | Neuroma | Hypercholesterolemia, Familial | Apert Syndrome | Syphilis | Paracoccidioidomycosis | Diffuse Intrinsic Pontine Glioma | Temporal Lobe Epilepsy | Spondylolisthesis | Acrocallosal Syndrome | Infantile Spasm | Thrombotic Microangiopathy | Stevens-Johnson Syndrome | Spondyloperipheral Dysplasia | Thyroiditis, Autoimmune | Nephritis, Interstitial | Pseudo-pseudohypoparathyroidism | Scleroderma, Diffuse | Familial Pheochromocytoma-paraganglioma | Mast Cell Leukemia | Congenital Myopathy | Sclerocornea | Coronary Restenosis | Chondrodysplasia Punctata | Leprosy | Hypertelorism | Multiple Myeloma | Histiocytosis | Teratozoospermia | Dermatomyositis | Infectious Diarrhea | Hemochromatosis Type 1 | Lamellar Ichthyosis | Gynecomastia | Barrett Esophagus | Basan Syndrome | Long QT Syndrome Type 3 | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Beta-Propeller Protein-associated Neurodegeneration | Strabismus | Sickle Cell Anemia | Glioma | Multiple Epiphyseal Dysplasia | Keratoacanthoma | Schizophrenia | DEND Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Primary Aldosteronism | Menetrier Disease | Hemosiderosis | Treacher Collins Syndrome | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Peters-plus Syndrome | Leiomyoma | Trimethylaminuria | Congenital Diaphragmatic Hernia | Craniosynostosis | Scabies | Pfeiffer Syndrome | 3-M Syndrome | NGLY1 Deficiency | Blepharitis | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Tyrosinemia Type 2 | Cocaine-Related Disorders | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Rickets | Diffuse Palmoplantar Keratoderma | Charcot-Marie-Tooth Disease Type 4D | Jawad Syndrome | Osteogenesis Imperfecta Type III | Tay-Sachs Disease | Methemoglobinemia | Pigment Dispersion Syndrome | Persistent Mullerian Duct Syndrome | Wolfram Syndrome 2 | Burn-McKeown Syndrome | Klinefelter Syndrome | Macular Corneal Dystrophy Type 1 | Myelitis | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Angiosarcoma Of The Breast | Fetal Alcohol Syndrome | Withdrawal Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Spitz Nevus | Hereditary Xerocytosis | Granular Corneal Dystrophy | Erythema Nodosum | Schamberg Disease | Blue Nevus | Myelitis, Transverse | Dent Disease | Chronic Lymphocytic Leukemia | Familial Dysautonomia | Inflammatory Joint Disease | Osteogenesis Imperfecta Type V | Osteosclerosis | Spinocerebellar Ataxia Type 23 | Charcot-Marie-Tooth Disease Type 4E | Progressive Familial Intrahepatic Cholestasis | Citrullinemia | Agoraphobia | Osteoporosis, Postmenopausal | Haim-Munk Syndrome | Hepatitis A | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Chronic Granulomatous Disease, X-linked | Multiple Hamartoma Syndrome | Rhizomelic Chondrodysplasia Punctata | Epidermolytic Hyperkeratosis | Endometritis | Glutaric Aciduria Type 3 | Nutrition Disorders | Spinocerebellar Ataxia Type 27 | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Cerebellofaciodental Syndrome | Angelman Syndrome | LRBA Deficiency | Blastoma, Pleuropulmonary | Megaloblastic Anemia | Osteoarthritis | Kernicterus | Acute Coronary Syndrome | Rhabdomyosarcoma, Alveolar | Neuromuscular Disorders | Carpal Tunnel Syndrome | Cockayne Syndrome | Hodgkin Lymphoma | Hypocalcemia | Pseudohypoparathyroidism Type 2 | Myotonic Disorders | Meconium Ileus | Motion Sickness | Temtamy Preaxial Brachydactyly Syndrome | Hydronephrosis | Stickler Syndrome | Headache | 3-methylglutaconic Aciduria Type IV | Tuberculous Meningitis | Poirier-Bienvenu Neurodevelopmental Syndrome | Lichen Sclerosus | Mitochondrial DNA Depletion Syndrome 13 | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | N-acetylglutamate Synthase Deficiency | Coenzyme Q10 Deficiency | Localized Scleroderma | Lymphoma, AIDS-related | Spinocerebellar Ataxia Type 31 | Oculocutaneous Albinism Type 1 | Atherosclerosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Hyperekplexia | Charcot-Marie-Tooth Disease | Myoclonus | Myosin Storage Myopathy | Encephalopathy, Hepatic | Tendinitis | Glycogen Storage Disease Type 0, Muscle | Mountain Sickness | Androgenic Alopecia | Familial Episodic Pain Syndrome | Hypotrichosis | Spitzoid Melanoma | Spastic Paraplegia Type 7 | Mitochondrial Myopathy | Congenital Heart Defects | Familial Cerebral Amyloid Angiopathy | Glaucoma, Congenital | 3-methylglutaconic Aciduria | Hereditary Hemorrhagic Telangiectasia | Tinea Versicolor | Infantile Nephropathic Cystinosis | Crisponi Syndrome | Cleidocranial Dysplasia | Iron Overload | Dermatitis | Dystonia | Neuroendocrine Cancer | Intestinal Hypomagnesemia 1 | Heart Failure | Pituitary Stalk Interruption Syndrome | X-linked Charcot-Marie-Tooth Disease | Leukocyte Adhesion Deficiency | Gangliosidosis | Fahr Disease | Ovarian Sex Cord-stromal Tumor | Hypersensitivity Pneumonitis | Tuberculosis | Familial Retinal Arterial Macroaneurysm | Vici Syndrome | Spinocerebellar Ataxia Type 21 | Lafora Disease | Polyneuropathy | Focal Cortical Dysplasia Type 2 | Prader-Willi Syndrome | Majeed Syndrome | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Adrenomyeloneuropathy | Hypokalemic Periodic Paralysis | Rash | Anodontia | Scleritis | Osteoporosis | Alpha-mannosidosis | Anencephaly | Schizencephaly | Basal Cell Nevus Syndrome