Disease

Retinal Telangiectasia

About the Disease
Retinal Telangiectasia is related to macular dystrophy, dominant cystoid and peripheral retinal degeneration. An important gene associated with Retinal Telangiectasia is CTC1 (CST Telomere Replication Complex Component 1), and among its related pathways/superpathways are "Cell Cycle, Mitotic" and Chromosome Maintenance. The drugs Ranibizumab and Angiogenesis Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include retina and myeloid, and related phenotypes are Increased shRNA abundance (Z-score > 2) and Increased shRNA abundance (Z-score > 2)

Common Targets
Vascular endothelial growth factors (VEGF) (nonspecified subtype)

疾病靶点研报
Retinal Telangiectasia

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

Other Diseases

Bicuspid Aortic Valve | Diabetic Neuropathy | Dent Disease | Pierson Syndrome | Erysipelas | Hypertension | Gray Platelet Syndrome | Epidermolytic Palmoplantar Keratoderma | Meningitis | Meniere's Disease | Cone Dystrophy | Subcortical Band Heterotopia | Acrodermatitis | Macrophagic Myofasciitis | Prader-Willi Syndrome | Thrombosis | Adenomyosis | Hypertension, Renal | Torticollis | Spinocerebellar Ataxia Type 8 | Milk Allergy | Sarcoma, Endometrial Stromal | Colitis, Collagenous | Hemochromatosis Type 1 | Charcot-Marie-Tooth Disease Axonal Type 2N | Keratosis, Seborrheic | Microcephaly, Seizures, And Developmental Delay | Carpal Tunnel Syndrome | Chromosome 16p11.2 Deletion Syndrome | Hyperuricemia | Cramp Fasciculation Syndrome | Carpenter Syndrome | Trimethylaminuria | Preaxial Polydactyly | Vitamin A Deficiency | Platelet Disorders | Spinocerebellar Ataxia Type 6 | Fucosidosis | Histiocytic Sarcoma | Meningioma | Thyroid Hormone Resistance | Seminoma | Hemimegalencephaly | Hypersensitivity | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Thanatophoric Dysplasia Type 1 | Nicotine Dependence | Myoclonus | Rhabdomyosarcoma | Hyperparathyroidism, Primary | Saul-Wilson Syndrome | Corneal Dystrophy And Perceptive Deafness | Porphyria, Acute Intermittent | Brenner Tumor | Seasonal Mood Disorder | Pterygium | Polycystic Liver | Alagille Syndrome | Rash | Diabetic Macular Edema | Left Ventricular Noncompaction | Holoprosencephaly | Neurodevelopmental Disorders | Glutaric Aciduria Type 3 | Chondromyxoid Fibroma | Autosomal Recessive Congenital Ichthyosis | Aplasia Cutis Congenita | Charcot-Marie-Tooth Disease Type 2T | Hypotonia-cystinuria Syndrome | Posterior Polar Cataract | Superficial Spreading Melanoma | Intestinal Pseudo-obstruction | Atopy | Pseudo-pseudohypoparathyroidism | Porphyria Cutanea Tarda | Myoclonus-dystonia Syndrome | Sporadic Inclusion Body Myositis | Atelosteogenesis Type 2 | Mucolipidosis Type III | Autoimmune Hemolytic Anemia | Blepharospasm | Low Phospholipid Associated Cholelithiasis | Glycogen Storage Disease | Hyperekplexia | Postpartum Depression | Thyrotoxic Periodic Paralysis | Mitochondrial Cytopathy | Carbamoyl Phosphate Synthetase I Deficiency | Congestive Heart Failure | X-linked Myotubular Myopathy | Endometrial Hyperplasia | Anovulation | Pycnodysostosis | Autonomic Neuropathy | Light Chain Amyloidosis | Stickler Syndrome | Paternal Uniparental Disomy Of Chromosome 14 | Familial Glucocorticoid Deficiency | NDH Syndrome | Multiple Hamartoma Syndrome | Protein S Deficiency | HIBCH Deficiency | Batten Disease | Angelman Syndrome | Non-Hodgkin Lymphoma | Periventricular Leukomalacia | Microtia | Primary Carnitine Deficiency | Alpha-mannosidosis | Pituitary Disorders | Netherton Syndrome | Neuroblastoma | Stargardt Disease | Reye Syndrome | Lymphomatoid Granulomatosis | Behcet's Disease | Hypocalcemia | Renal Tubular Dysgenesis | Hemolytic Uremic Syndrome | Carcinoid Tumor | Hereditary Coproporphyria | Inborn Errors Of Metabolism | Impetigo | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Lipid Metabolism Disorders | Cold-induced Sweating Syndrome | Schizencephaly | Endometriosis | Pontocerebellar Hypoplasia Type 7 | Vitelliform Macular Dystrophy | Erythematotelangiectatic Rosacea | Pseudoachondroplasia | Anorectal Malformations | Connective Tissue Disorders | Scapuloperoneal Spinal Muscular Atrophy | Zygomycosis | Obesity, Morbid | Systemic Lupus Erythematosus | Galloway-Mowat Syndrome | VEXAS Syndrome | Duane Retraction Syndrome | Ophthalmoplegia | Waardenburg Syndrome Type 2A | Pancreatitis, Chronic | Chronic Kidney Disease | Hypokalemic Periodic Paralysis | Wolfram Syndrome 2 | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Cardiomyopathy, Dilated, 1L | Esophagitis, Eosinophilic | Polydactyly | Urofacial Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Diarrhea | Dermatofibrosarcoma | Spinal And Bulbar Muscular Atrophy | KBG Syndrome | Dystonia | Glycogen Storage Disease Type 9 | Stuttering | Chondrodysplasia Punctata 1, X-linked Recessive | Pupil Disorders | Myasthenia | Werner's Syndrome | Presbycusis | Blepharitis | Retinitis Pigmentosa | Leukoplakia, Oral | Granular Corneal Dystrophy Type 1 | Pontocerebellar Hypoplasia | Sweet Syndrome | SAPHO Syndrome | Patent Foramen Ovale | Optic Atrophy 2 | Rickets | Sengers Syndrome | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Epidermodysplasia Verruciformis | Retinopathy, Diabetic | Goiter | Polymyositis | C3 Glomerulopathy | Angiodysplasia | FG Syndrome | Dysfibrinogenemia | Irritable Bowel Syndrome | Papilledema | 3C Syndrome | Gyrate Atrophy Of The Choroid And Retina | Speech Disorders | Nephronophthisis | Marinesco-Sjogren Syndrome | Mixed Connective Tissue Disease | Pulverulent Zonular Cataract | Retinopathy Of Prematurity | Metanephric Adenoma | Chronic Leukemia | Carcinoid Syndrome | Prolymphocytic Leukemia | Axenfeld-Rieger Syndrome | CHARGE Syndrome | Zimmermann-Laband Syndrome | Epiphyseal Chondrodysplasia, Miura Type | DNA Ligase IV Deficiency | Heterotaxy | Congenital Dyserythropoietic Anemia Type 1 | Antithrombin III Deficiency | Onchocerciasis | Osteopetrosis | Stomatitis | Amyotrophic Lateral Sclerosis, Juvenile | Cerebrotendinous Xanthomatosis | Beta-Propeller Protein-associated Neurodegeneration | Purpura | Trichorhinophalangeal Syndrome | Takotsubo Cardiomyopathy | Paronychia | Genee-Wiedemann Syndrome | Heart Septal Defects | Mitochondrial DNA Depletion Syndrome | Erdheim-Chester Disease | Shwachman-Bodian-Diamond Syndrome | Chorea | Glaucoma | Hypereosinophilic Syndrome | Yellow Fever | Optic Neuropathy, Anterior Ischemic | Malaria, Cerebral | Hypoplastic Left Heart Syndrome | Zellweger Syndrome | Enterocolitis, Necrotizing | Scabies | Cervical Dystonia | Astrocytoma, Anaplastic | Teratozoospermia | Myoclonic Atonic Epilepsy | Lymphoma | Alopecia Totalis | Myotonic Disorders | Glycogen Storage Disease Type 6 | Optic Nerve Hypoplasia, Bilateral | Paraplegia | Apraxia | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Cocaine-Related Disorders | Dyskeratosis Congenita | Obsessive-compulsive Disorder | Common Variable Immunodeficiency | Myosin Storage Myopathy | Hepatitis B, Chronic | Hypertension, Portal | Carney-Stratakis Syndrome | Conjunctivitis, Allergic | Subacute Sclerosing Panencephalitis | Neurofibroma | Cheilitis | Astigmatism | Cousin Syndrome | Craniopharyngioma | Supravalvular Aortic Stenosis | Exotropia | Leukoencephalopathy, Progressive Multifocal | Sitosterolemia | Necrotizing Autoimmune Myopathy | HANAC Syndrome | Oligospermia | Thrombocytopenia | Cole-Carpenter Syndrome | Erythema Nodosum | Polyneuropathy | Camurati-Engelmann Disease | Chronic Thromboembolic Pulmonary Hypertension | Anorchia | Craniofrontonasal Syndrome | Sarcoidosis | Congenital Sodium Diarrhea | Reticular Dysgenesis | Genitopatellar Syndrome | Carbohydrate Metabolism Disorders | Bipolar Disorder | Dementia, Vascular | Lymphoproliferative Disease, X-linked | Renal Hypomagnesemia 3 | Spinocerebellar Ataxia | Waardenburg Syndrome Type 2 | N-acetylglutamate Synthase Deficiency | Xeroderma Pigmentosum Variant Type | Angioedema | Sertoli Cell-only Syndrome | Diabetic Nephropathy | Pemphigus Foliaceus | Skin Carcinoma | Dermatomyositis | Lymphoma, Follicular | Skin Fragility-woolly Hair Syndrome | Familial Advanced Sleep Phase Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Hashimoto Thyroiditis | Gangliosidosis | Nephrotic Syndrome | Immunoproliferative Disorders | Klinefelter Syndrome | Sarcoma, Alveolar Soft Part | Chylomicron Retention Disease | Odonto-onycho-dermal Dysplasia | Dengue Hemorrhagic Fever | Vitiligo | Borjeson-Forssman-Lehmann Syndrome | Congenital Bilateral Absence Of Vas Deferens | AIDS Dementia Complex | Myopia | Hypertensive Nephropathy | Amblyopia | Cancer, Breast | Esophageal Carcinoma | Mastitis | Nutrition Disorders | Congenital Muscular Dystrophy | Tay-Sachs Disease | Birk-Barel Syndrome | Generalized Epilepsy With Febrile Seizures Plus | Rheumatoid Arthritis | Alcoholism | ICF Syndrome | Placenta Previa | Pure Red Cell Aplasia | Citrullinemia | Basal Ganglia Disease | Carcinoma, Transitional Cell | Fowler's Syndrome | Basal Ganglia Cerebrovascular Disease | Congenital Heart Defects | Pineoblastoma | Isovaleric Acidemia | Stroke, Ischemic | Thanatophoric Dysplasia | Arts Syndrome | Endocarditis | Low Tension Glaucoma | Gingivitis | Niemann-Pick Disease, Type A | Macrodactyly | Micropenis | Canavan Disease | Kabuki Syndrome | Lymphangioma | Antisynthetase Syndrome | Poikiloderma With Neutropenia | Androgenic Alopecia | Benign Hereditary Chorea | Temporal Lobe Epilepsy | Pyruvate Decarboxylase Deficiency | Ocular Hypertension | Progressive Familial Intrahepatic Cholestasis | Prurigo Nodularis | Muckle-Wells Syndrome | Hepatitis, Alcoholic | Spinocerebellar Ataxia Type 7 | Dysthymia | Juvenile Myelomonocytic Leukemia | Muscle Wasting | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Meningioma, Benign | Epidermolysis Bullosa Acquisita | Kabuki Syndrome 2 | Calcium Pyrophosphate Deposition Disease | Wieacker-Wolff Syndrome | Asphyxia Neonatorum | Hypokalemia | Pituitary Dwarfism | Primary Aldosteronism | Pituitary Stalk Interruption Syndrome | Rhabdoid Tumor | Encephalitis | Nephropathy | Fibrosis | Endometritis | Cryopyrin-associated Periodic Syndromes | Orotic Aciduria | Haim-Munk Syndrome | Dyggve-Melchior-Clausen Disease | Congenital Central Hypoventilation Syndrome | Renal Tubular Acidosis | Nephrotic Syndrome Type 1 | Spondylolisthesis | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Polyradiculopathy | Myotonia | Neuroendocrine Cancer | Gnathodiaphyseal Dysplasia | Parkinson Disease 6, Autosomal Recessive Early-onset | Essential Fructosuria | X-linked Sideroblastic Anemia | Coloboma | Spondylocostal Dysostosis | Dentinogenesis Imperfecta | Pierre Robin Syndrome | Keloid | Anxiety Disorders | Scoliosis