Familial Exudative Vitreoretinopathy
Familial Exudative Vitreoretinopathy
About the Disease
Exudative Vitreoretinopathy, also known as familial exudative vitreoretinopathy, is related to exudative vitreoretinopathy 1 and vitreoretinopathy. An important gene associated with Exudative Vitreoretinopathy is LRP5 (LDL Receptor Related Protein 5), and among its related pathways/superpathways are Nanog in Mammalian ESC Pluripotency and Signaling by WNT. The drugs Bromfenac and Anti-Inflammatory Agents, Non-Steroidal have been mentioned in the context of this disorder. Affiliated tissues include retina, eye and bone, and related phenotypes are vitreoretinopathy and peripheral retinal avascularization
Common Targets
CTNNA1 | SOX17 | LRP5 | ILK | FZD4 | DLG1 | CRX | RS1 | JAG1 | RCBTB1 | CTNNB1 | ATOH7 | TSPAN12 | KIF11 | RIMS1 | BEST1 | NDP | CAPN5 | ZNF408

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Other Diseases
Cardiomyopathy, Peripartum | Microcephaly | Hyperparathyroidism, Secondary | Combined Deficiency Of Factor V And Factor VIII | Neurocutaneous Melanocytosis | Arthrogryposis | Polyradiculopathy | Blepharoconjunctivitis | Myosin Storage Myopathy | Oligospermia | Osteonecrosis | Hyperuricemia | Myasthenia | Autism | Non-bullous Congenital Ichthyosiform Erythroderma | Congenital Myasthenic Syndrome | Peters-plus Syndrome | Rotor Syndrome | Spinocerebellar Ataxia Type 1 | Spinocerebellar Ataxia Type 20 | Craniofrontonasal Syndrome | Lattice Corneal Dystrophy | Emery-Dreifuss Muscular Dystrophy | Apert Syndrome | Paroxysmal Nocturnal Hemoglobinuria | Tetraplegia | Agnathia-Otocephaly Complex | Keratitis | Rhabdoid Tumor | Optic Neuritis | Adenoma, Pituitary | Amyloidosis | Brachydactyly | Congenital Adrenal Hyperplasia 1 | Neural Tube Defect | Craniosynostosis | Primary Progressive Nonfluent Aphasia | Citrullinemia | Ichthyosis Hystrix, Curth-Macklin Type | Granular Corneal Dystrophy Type 1 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Odonto-onycho-dermal Dysplasia | Erysipelas | LRBA Deficiency | Cold Agglutinin Disease | Photosensitivity | Mucolipidosis Type III | Mast Cell Leukemia | Progressive Myoclonic Epilepsy | Melanoma, Uveal | Depression | Cerebrotendinous Xanthomatosis | Intermittent Claudication | Acute Generalized Exanthematous Pustulosis | Amenorrhea | Ovarian Hyperstimulation Syndrome | Congenital Bile Acid Synthesis Defect | Infertility, Male | Cockayne Syndrome | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Ovarian Sex Cord-stromal Tumor | Early Infantile Epileptic Encephalopathy | Pyruvate Carboxylase Deficiency Disease | Poikiloderma With Neutropenia | Hepatoblastoma | Multiple Sulfatase Deficiency | Autosomal Recessive Spastic Paraplegia Type 54 | Sturge-Weber Syndrome | Spinal And Bulbar Muscular Atrophy | Lesch-Nyhan Syndrome | Bipolar Disorder | CEDNIK Syndrome | Jalili Syndrome | Acromesomelic Dysplasia | Acute Anterior Uveitis | Optic Neuropathy, Anterior Ischemic | 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Amblyopia | Cyclic Vomiting Syndrome | Uterine Leiomyoma | T-cell Lymphoma, Subcutaneous Panniculitis-like | Primary Lateral Sclerosis | Proctitis | Hereditary Hemorrhagic Telangiectasia | Poirier-Bienvenu Neurodevelopmental Syndrome | Specific Granule Deficiency | Cholera | Silicosis | Chronic Granulomatous Disease | Hepatitis, Autoimmune | Proximal Symphalangism | Rhabdomyosarcoma, Embryonal | Methylmalonic Aciduria And Homocystinuria, CblC Type | Vitelliform Macular Dystrophy | Ebstein Anomaly | Cutaneous T-cell Lymphoma | Myocarditis | Colon Adenoma | Tinea | Van Der Knaap Disease | Duane Retraction Syndrome | Lymphoma, Follicular | Liver Failure | Lymphangiomatosis | Hypobetalipoproteinemias | Intestinal Hypomagnesemia 1 | Nephrosclerosis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Canavan Disease | Juvenile Xanthogranuloma | Hypoglycemia | Wiedemann-Steiner Syndrome | Charcot-Marie-Tooth Disease Type 4D | Kindler Syndrome | Chronic Beryllium Disease | Stuttering | Sick Sinus Syndrome 1 | Frank-ter Haar Syndrome | Cabezas Syndrome | Early Infantile Epileptic Encephalopathy 1 | Aicardi-Goutieres Syndrome | Chronic Periodontitis | Keratoconjunctivitis | Fibrosarcoma | Dementia | Hyperlipidemia, Familial Combined | Supravalvular Aortic Stenosis | Guttate Psoriasis | Pleural Tuberculosis | Plasma Cell Dyscrasia | Chorioretinitis | Fahr Disease | Angiosarcoma | Microphthalmia | Multisystemic Smooth Muscle Dysfunction Syndrome | Periventricular Nodular Heterotopia | Retinal Diseases | Hypolipoproteinemia | Sporadic Hemiplegic Migraine | Polymicrogyria | Meconium Ileus | Primary Aldosteronism | Carotid Artery Disease | Olmsted Syndrome | Hepatitis D | Chordoid Glioma | Pelvic Inflammatory Disease | Iron Deficiency Anemia | Glioblastoma | Blood Protein Disorders | Primrose Syndrome | Congenital Lipoid Adrenal Hyperplasia | Sarcoma, Ewing | Joubert Syndrome | Bacterial Meningitis | Wolff-Parkinson-White Syndrome | Molybdenum Cofactor 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