Disease

Lattice Corneal Dystrophy Type 1

About the Disease
Corneal Dystrophy, Lattice Type I, also known as lattice corneal dystrophy type i, is related to corneal dystrophy and lattice corneal dystrophy. An important gene associated with Corneal Dystrophy, Lattice Type I is TGFBI (Transforming Growth Factor Beta Induced), and among its related pathways/superpathways is Coregulation of Androgen receptor activity. Affiliated tissues include eye, and related phenotypes are corneal scarring and lattice corneal dystrophy

Common Targets
TGFBI

疾病靶点研报
Lattice Corneal Dystrophy Type 1

Note: If you'd like to get a target analysis report for Lattice Corneal Dystrophy Type 1, 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 Lattice Corneal Dystrophy Type 1 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Glaucoma, Congenital | Pulmonary Alveolar Proteinosis | Borderline Personality Disorder | Hyperparathyroidism, Secondary | Anal Fissure | Neuromyelitis Optica | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Postaxial Polydactyly | Metaphyseal Chondrodysplasia, Schmid Type | Sandhoff Disease | Wilson's Disease | Benign Familial Infantile Seizures | Gastroenteritis, Eosinophilic | Hydrops Fetalis | Benign Familial Neonatal Convulsions | Hypotonia-cystinuria Syndrome | Pyruvate Carboxylase Deficiency Disease | Charcot-Marie-Tooth Disease Type 4D | Pulmonary Veno-occlusive Disease | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Maternally Inherited Diabetes And Deafness | Nephrotic Syndrome Type 1 | Epidermolysis Bullosa Simplex, Generalized | Blau Syndrome | Polymyalgia Rheumatica | Arts Syndrome | Corneal Dystrophies, Hereditary | Spinocerebellar Ataxia Type 28 | Birt-Hogg-Dube Syndrome | Avian Influenza | Hypocalcemia | Pain | Huntington's Disease | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Delirium | Benign Hereditary Chorea | Necrobiosis Lipoidica | Hyperinsulinemic Hypoglycemia | Nemaline Myopathy | Neurodegeneration With Brain Iron Accumulation | Primary Lateral Sclerosis | Antenatal Bartter Syndrome Type 1 | Alveolar Capillary Dysplasia | Mitochondrial Cytopathy | Brooke-Spiegler Syndrome | Joubert Syndrome 2 | Polyomavirus Nephropathy | Osteogenesis Imperfecta Type I | Prediabetes | Coronary Artery Disease | Maple Syrup Urine Disease | Epithelial-myoepithelial Carcinoma | Kawasaki Disease | Tyrosinemia Type 2 | Keratosis | Neuromuscular Disorders | Oligoasthenoteratozoospermia | Spinocerebellar Ataxia Type 1 | Wolcott-Rallison Syndrome | Focal Cortical Dysplasia Type 2 | Bulimia Nervosa | Basal Cell Nevus Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Glaucoma | Juvenile Myoclonic Epilepsy | Sarcomatoid Carcinoma Of The Lung | Dupuytren Disease | Cardiomyopathy, Hypertrophic | Ischemia | Lysosomal Acid Lipase Deficiency | Cardiomyopathy, Dilated, 1L | Communication Disorders | Pulmonary Alveolar Microlithiasis | Giant Cell Arteritis | Salla Disease | Shprintzen-Goldberg Syndrome | Uveitis, Anterior | Glomerulonephritis, Membranous | Hypercholesterolemia | Syncope | Myofibrillar Myopathy | Osteoporosis | Angioedema | Guttate Psoriasis | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Sporadic Hemiplegic Migraine | Mitochondrial DNA Depletion Syndrome | Vitreoretinopathy, Proliferative | Congestive Heart Failure | McKusick Type Metaphyseal Chondrodysplasia | Juvenile Hyaline Fibromatosis | Lichen Sclerosus | Cholecystitis | Pulmonary Capillary Hemangiomatosis | Acute Anterior Uveitis | Weill-Marchesani Syndrome | Hypermethioninemia | Mood Disorder | Potocki-Shaffer Syndrome | Dermatomyositis | Spinal Muscular Atrophy Type 3 | Rhabdomyosarcoma, Embryonal | Usher Syndrome Type II | Usher Syndrome | Tyrosine Hydroxylase Deficiency | Trichotillomania | Primary Progressive Nonfluent Aphasia | Short-chain Acyl-CoA Dehydrogenase Deficiency | Strabismus | Astrocytoma, Anaplastic | Proctitis | Bronchiolitis | Chronic Enteropathy Associated With SLCO2A1 Gene | Meningeal Melanocytoma | Spinocerebellar Ataxia Type 12 | Achromatopsia | Intestinal Pseudo-obstruction | Hartnup Disease | Non-bullous Congenital Ichthyosiform Erythroderma | Prune Belly Syndrome | Poretti-Boltshauser Syndrome | SAPHO Syndrome | Proopiomelanocortin Deficiency | Waardenburg Syndrome Type 1 | Epidermolysis Bullosa Simplex, Localized | Cancer, Prostate | Autoimmune Hemolytic Anemia | Epidermolysis Bullosa Acquisita | Fetal Akinesia Deformation Sequence | Charcot-Marie-Tooth Disease Type 4B1 | Vertigo | Neonatal Progeroid Syndrome | Coronary Heart Disease | Cryptococcal Meningitis | Feingold Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Lateral Meningocele Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Hemosiderosis | Toxoplasmosis | Optic Neuropathy, Anterior Ischemic | Schizoaffective Disorder | Fibrosis | Gangliosidosis | Follicular Dendritic Cell Sarcoma | Amyotrophic Lateral Sclerosis, Juvenile | Hyperlipidemia Type V | Plasma Cell Leukemia | Thrombophilia | Adrenomyeloneuropathy | Intestinal Hypomagnesemia 1 | Ectopia Lentis, Isolated, Autosomal Recessive | Thrombophlebitis | Familial Dysautonomia | Thalassemia, Beta | Myopathy | Hepatic Adenomatosis | Johanson-Blizzard Syndrome | Cockayne Syndrome | Inflammatory Myopathy | Congenital Stationary Night Blindness | Pyruvate Kinase Deficiency | Hypogonadism | Trichomegaly | Nevus | Methylmalonic Aciduria And Homocystinuria, CblC Type | Farber Disease | DICER1 Syndrome | Nasodigitoacoustic Syndrome | Rothmund-Thomson Syndrome | Fahr Disease | Sarcoidosis | Protein C Deficiency | Campomelic Dysplasia | Congenital Nephrotic Syndrome | Glycogen Storage Disease Type 3 | Autosomal Recessive Spastic Paraplegia Type 54 | Pterygium | Vasculitis | Chitayat Syndrome | Mumps | DiGeorge Syndrome | ADNP Syndrome | Panic Disorder | Peritonitis | N-acetylglutamate Synthase Deficiency | Hypopituitarism | Aspartylglycosaminuria | Blue Rubber Bleb Nevus Syndrome | Restrictive Dermopathy | Hypohidrotic Ectodermal Dysplasia, X-linked | Angiosarcoma Of The Breast | Gastritis, Atrophic | Coronary Restenosis | Esophagitis | Osteogenesis Imperfecta Type III | Infertility, Male | Meningococcal Infections | Metanephric Adenoma | Cavitary Optic Disc Anomalies | Rhinitis | Pancytopenia | Ameloblastoma | Obesity | Acute Kidney Injury | Alpha-mannosidosis | Encephalopathy, Glycine | Discoid Lupus Erythematosus | Cushing Syndrome | Optic Neuropathy | Spasticity | Acromesomelic Dysplasia | Histoplasmosis | Congenital Diaphragmatic Hernia | Hepatitis, Autoimmune | Progressive Myoclonic Epilepsy | Kleine-Levin Syndrome | Microphthalmia | Branchiootorenal Syndrome | Costello Syndrome | Glutaric Aciduria Type 3 | Leukodystrophies | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Hypothyroidism | Lennox-Gastaut Syndrome | Cystinosis | Proteus Syndrome | Chronic Thromboembolic Pulmonary Hypertension | Calcium Pyrophosphate Deposition Disease | Carcinoid Tumor | Dyskeratosis Congenita | Adenosine Deaminase Deficiency | Angiomyolipoma | Christianson Syndrome | Tendinopathy | Optic Nerve Hypoplasia, Bilateral | Jacobsen Syndrome | Myelomeningocele | Tay-Sachs Disease | Liddle Syndrome | Scabies | Benign Recurrent Intrahepatic Cholestasis 1 | Seborrheic Dermatitis | Paternal Uniparental Disomy Of Chromosome 14 | Carbamoyl Phosphate Synthetase I Deficiency | Batten Disease | Smoldering Myeloma | Otopalatodigital Syndrome Type 2 | Granular Corneal Dystrophy | Pyruvate Decarboxylase Deficiency | Niemann-Pick Disease | Chromosome 17q21.31 Deletion Syndrome | Meier-Gorlin Syndrome | Duchenne Muscular Dystrophy | Osteogenesis Imperfecta | Anemia | Schwannomatosis | Congenital Myopathy | Gliosarcoma | Brenner Tumor | Mixed Connective Tissue Disease | Epidermolysis Bullosa Dystrophica | Familial Retinal Arterial Macroaneurysm | Aneurysm, Abdominal Aortic | Hereditary Mixed Polyposis Syndrome | Cluster Headache | Conn Syndrome | NGLY1 Deficiency | Intermittent Explosive Disorder | Fuchs Dystrophy | Hyperphenylalaninemia | Axenfeld-Rieger Syndrome | Pulmonary Vein Stenosis | L-2-Hydroxyglutaric Aciduria | Behcet's Disease | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Retinal Dystrophy, Early-onset Severe | Ocular Hypertension | Orotic Aciduria | Congenital Dyserythropoietic Anemia | Leukoplakia, Oral | Congenital Lipoid Adrenal Hyperplasia | Primary Carnitine Deficiency | Chondrosarcoma | Diabetes Insipidus, Nephrogenic | VACTERL Association | Central Core Disease | VACTERL/VATER Association | Hypertension | Eosinophilia | Optic Nerve Diseases | Cardiomyopathy, Peripartum | Gastroenteritis | Familial Hemiplegic Migraine | Abetalipoproteinemia | Cerebrotendinous Xanthomatosis | Pemphigus Foliaceus | Erythropoietic Protoporphyria | Iron Metabolism Disorders | Parapsoriasis | Angiodysplasia | Vascular Calcification | Eating Disorder | Congenital Generalized Lipodystrophy | Exfoliative Dermatitis | Spinocerebellar Ataxia Type 31 | Obesity, Morbid | Coloboma | Adenocarcinoma | Pemphigus | Polymyositis | Presbycusis | 3-methylglutaconic Aciduria Type IV | Demyelinating Diseases | Renal Hypouricemia | Congenital Heart Block | Still Disease | Lyme Disease | Thyroid Dyshormonogenesis | Sponastrime Dysplasia | Subcortical Band Heterotopia | Neuroectodermal Tumors, Primitive | McCune-Albright Syndrome | Metachromatic Leukodystrophy | Transthyretin-related Amyloidosis | Muscular Dystrophy | Carcinoma, Small Cell | Hypodontia | Mitochondrial DNA Depletion Syndrome 13 | Aldosteronism | Isovaleric Acidemia | Goiter, Nodular | Thalassemia | Spinocerebellar Ataxia Type 13 | Poirier-Bienvenu Neurodevelopmental Syndrome | Chorioretinitis | Tuberculosis | Parkinson Disease 6, Autosomal Recessive Early-onset | Ulcerative Colitis | Hypopigmentation | Cutaneous Lupus Erythematosus | PASLI Disease | Esophageal Carcinoma | Myocardial Infarction | Rhabdomyosarcoma | Netherton Syndrome | Xeroderma Pigmentosum Variant Type | Anuria | Primary Torsion Dystonia | Spinocerebellar Ataxia Type 40 | Nance-Horan Syndrome | Familial Isolated Hyperparathyroidism | Adrenoleukodystrophy, X-linked | Personality Disorders | Charcot-Marie-Tooth Disease, Type 1A | Hairy Cell Leukemia | Epicondylitis | Imerslund-Grasbeck Syndrome | Hyperprolactinemia | Goiter | Non-proliferative Diabetic Retinopathy | Tuberculous Meningitis | Retinal Coloboma | Stromal Corneal Dystrophy | Central Retinal Artery Occlusion | Malignant Peripheral Nerve Sheath Tumor | Chylothorax, Congenital | Glycogen Storage Disease Type 0 | Epidermolytic Palmoplantar Keratoderma | Diverticulitis | Danon Disease | LRBA Deficiency | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Corneal Ulcer | Blastoma, Pleuropulmonary | Nicotine Addiction | Idiopathic Multicentric Castleman Disease | Fabry's Disease | Adenomatoid Tumor | Rickets | Periventricular Nodular Heterotopia | Hyperinsulinemia | Combined Deficiency Of Factor V And Factor VIII | Multiple Sclerosis | Priapism | Spinocerebellar Ataxia Type 20 | Tatton-Brown-Rahman Syndrome | Chromosome 9q34.3 Deletion Syndrome | Knobloch Syndrome | Congenital Disorders Of Glycosylation Type II | Skin Carcinoma | Congenital Fiber-type Disproportion Myopathy | Hypercalcemia | Neutropenia | Endometritis | Endometrial Hyperplasia | X-linked Creatine Transporter Deficiency | Progressive Familial Intrahepatic Cholestasis Type 2 | Diffuse Intrinsic Pontine Glioma | Vitamin D Deficiency