Disease

Fuchs Heterochromic Iridocyclitis

About the Disease
Fuchs' Heterochromic Uveitis, also known as fuchs heterochromic iridocyclitis, is related to retinal vasculitis and macular dystrophy, dominant cystoid. An important gene associated with Fuchs' Heterochromic Uveitis is TGFB2 (Transforming Growth Factor Beta 2), and among its related pathways/superpathways are ERK Signaling and MIF Mediated Glucocorticoid Regulation. Affiliated tissues include eye, endothelial and t cells, and related phenotypes are homeostasis/metabolism and neoplasm

Common Targets
WAKMAR2 | TNFAIP3

疾病靶点研报
Fuchs Heterochromic Iridocyclitis

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

Other Diseases

Gitelman Syndrome | Cyst | Acute Chest Syndrome | Primary Cutaneous Amyloidosis | Cataract | Werner's Syndrome | Tenosynovial Giant Cell Tumor | Erysipelas | Primary Pigmented Nodular Adrenocortical Disease | Lupus Erythematosus | Schizoaffective Disorder | Aldosterone Synthase Deficiency | Transient Bullous Dermolysis Of The Newborn | Niemann-Pick Disease, Type B | Congenital Fiber-type Disproportion Myopathy | Prolactinoma | Intermittent Claudication | Melanoma, Uveal | Subacute Sclerosing Panencephalitis | Dwarfism | Waardenburg Syndrome Type 2A | Focal Dermal Hypoplasia | Infantile Liver Failure Syndrome 1 | Bainbridge-Ropers Syndrome | Pituitary Dwarfism | Shprintzen-Goldberg Syndrome | Osteogenesis Imperfecta Type IV | Limb Girdle Muscular Dystrophy | Duchenne Muscular Dystrophy | Pitt-Hopkins Syndrome | Erdheim-Chester Disease | Kabuki Syndrome | Photosensitivity | Congenital Bilateral Absence Of Vas Deferens | Spinocerebellar Ataxia Type 8 | Pelizaeus-Merzbacher Disease | Ichthyosis, X-linked | Sick Sinus Syndrome 1 | Spinocerebellar Ataxia Type 13 | Cystinosis | Anemia | Thrombocytopenia | Sjogren Syndrome | Leprosy | Cholangiocarcinoma | Arthrogryposis | Thrombophlebitis | Urticaria | Saethre-Chotzen Syndrome | Vici Syndrome | Leri Pleonosteosis | Hoyeraal-Hreidarsson Syndrome | Vitreoretinopathy, Proliferative | Congenital Aniridia | Osteitis | Fucosidosis | Cholestasis | Goiter | Arthritis, Psoriatic | Charcot-Marie-Tooth Disease Type 3 | Celiac Disease | Endometriosis | Rhabdoid Tumor | Congenital Hereditary Endothelial Dystrophy Type II | Castleman Disease | Patent Foramen Ovale | Congenital Lipoid Adrenal Hyperplasia | Corneal Ulcer | Chronic Lymphocytic Leukemia | Scapuloperoneal Spinal Muscular Atrophy | Myotonia | X-linked Sideroblastic Anemia | Niemann-Pick Disease, Type C | Primary Hyperoxaluria | Renal-hepatic-pancreatic Dysplasia | Mountain Sickness | Adenoma, Villous | Multiple Myeloma | Insulin Resistance | Bethlem Myopathy | Aneurysm, Thoracic Aortic | Presbycusis | Pseudohermaphroditism | Graft-versus-host Disease | Cat Eye Syndrome | Heroin Dependence | Pre-eclampsia | Bardet-Biedl Syndrome | Hashimoto Thyroiditis | Rheumatoid Arthritis | Dermatitis Herpetiformis | Hydrocephalus | CEDNIK Syndrome | Leukocyte Adhesion Deficiency | Antisocial Personality Disorder | Atrial Septal Defect | Metaphyseal Chondrodysplasia, Schmid Type | Epidermolysis Bullosa Dystrophica | Familial Exudative Vitreoretinopathy | Intellectual Disability, Autosomal Dominant 5 | Blepharitis | Wolman Disease | Idiopathic Multicentric Castleman Disease | Blue Rubber Bleb Nevus Syndrome | Leber Hereditary Optic Neuropathy | Systemic Lupus Erythematosus | Central Pain Syndrome | Congenital Hypofibrinogenemia | Myotonic Disorders | Pontocerebellar Hypoplasia Type 7 | Seborrheic Dermatitis | Fahr Disease | Liebenberg Syndrome | Ghosal Syndrome | Thyrotoxic Periodic Paralysis | Hyperinsulinism-hyperammonemia Syndrome | Spinal Cord Diseases | Pycnodysostosis | Acral Lentiginous Melanoma | Japanese Encephalitis | Preaxial Polydactyly | Lassa Fever | Adenosine Deaminase Deficiency | Arteriovenous Malformations | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Lattice Corneal Dystrophy | Cutaneous T-cell Lymphoma | Hereditary Elliptocytosis | Tetraplegia | Sulfite Oxidase Deficiency | HELLP Syndrome | Myelomeningocele | Polycystic Ovary Syndrome | Chordoid Glioma | Hepatitis B, Chronic | Spinocerebellar Ataxia Type 1 | Necrobiosis Lipoidica | McKusick Type Metaphyseal Chondrodysplasia | Macrodactyly | Gyrate Atrophy Of The Choroid And Retina | Stomatitis | Asperger Syndrome | Alpha-1 Antitrypsin Deficiency | Renal Oncocytoma | Usher Syndrome Type IIC | Bone Marrow Necrosis | Hypertelorism | Anorexia Nervosa | Tay-Sachs Disease | Neuroectodermal Tumors, Primitive | Venous Insufficiency | Pure Autonomic Failure | Hemochromatosis Type 2 | Combined Pituitary Hormone Deficiency | Pseudohypoparathyroidism Type 1C | Cardiomyopathy, Hypertrophic | Congenital Generalized Lipodystrophy | Cutis Laxa | Proximal Symphalangism | Infantile Neuroaxonal Dystrophy | Pierson Syndrome | Myofibromatosis | Uterine Leiomyoma | ADNP Syndrome | Charcot-Marie-Tooth Disease Type 2T | Benign Hereditary Chorea | Tremor | Hypercholesterolemia, Familial | Hyperglycemia | Chondrodysplasia Punctata 1, X-linked Recessive | Multicentric Carpotarsal Osteolysis Syndrome | Carcinoma, Merkel Cell | Joubert Syndrome 2 | Cellulitis | Brugada Syndrome 1 | Rhizomelic Chondrodysplasia Punctata | Myhre Syndrome | Kaposiform Hemangioendothelioma | Neurofibromatosis Type 1 | Porphyria, Acute Intermittent | Urofacial Syndrome | Bronchiolitis | Chordoma | Impetigo | Ebstein Anomaly | Lymphoproliferative Disease, X-linked | Raine Syndrome | Myositis, Focal | Lymphoma | IgA Deficiency | Opisthorchiasis | Spinal Muscular Atrophy | Stroke, Ischemic | Pyruvate Carboxylase Deficiency Disease | Diabetic Nephropathy | Alpha-thalassemia Myelodysplasia Syndrome | Chanarin-Dorfman Syndrome | Acute Coronary Syndrome | Onchocerciasis | Coffin-Siris Syndrome | Lipoma | Optic Nerve Diseases | Esotropia | Angioedema, Hereditary | Primary Lateral Sclerosis | Vitelliform Macular Dystrophy | Hypereosinophilic Syndrome | Frank-ter Haar Syndrome | Hereditary Sensory And Autonomic Neuropathy | Allergic Contact Dermatitis | Progressive Familial Intrahepatic Cholestasis | Gastritis, Atrophic | Allan-Herndon-Dudley Syndrome | Hemangioendothelioma | Familial Glucocorticoid Deficiency | Neurofibroma, Plexiform | Benign Familial Neonatal Convulsions | Glycogen Storage Disease Type 4 | Keratoconus | Congenital Adrenal Hyperplasia | Kindler Syndrome | Pseudomyxoma Peritonei | Pearson Syndrome | Incontinentia Pigmenti | Congenital Dyserythropoietic Anemia | Plasmacytoma | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Erythema Multiforme | Parkinson's Disease | Endometrial Hyperplasia | Silver-Russell Syndrome | Spasticity | PASLI Disease | Primary Biliary Cholangitis | Greig Cephalopolysyndactyly Syndrome | Nasodigitoacoustic Syndrome | Hepatopulmonary Syndrome | Cervicitis | Achromatopsia | Kawasaki Disease | Guanidinoacetate Methyltransferase Deficiency | Carney Triad | Neurocutaneous Syndromes | Harlequin Ichthyosis | Infantile Refsum Disease | Varices | Keratosis | Ollier Disease | Aspergillosis | Progressive Familial Intrahepatic Cholestasis Type 2 | Cluster Headache | Glycogen Storage Disease Type 1a | Mucormycosis | Anosmia, Congenital | Fibromuscular Dysplasia | Distal Spinal Muscular Atrophy | Sarcoidosis | Netherton Syndrome | Congenital Hereditary Endothelial Dystrophy Type I | Splenomegaly | Noonan Syndrome | Guillain-Barre Syndrome | VACTERL/VATER Association | Usher Syndrome Type I | Retinoschisis | Hemorrhagic Disorders | Giant Axonal Neuropathy | Purpura, Thrombotic Thrombocytopenic | Myelodysplasia | Pituitary Stalk Interruption Syndrome | Melanoma | Dystonia-parkinsonism, X-linked | Blepharo-cheilo-odontic Syndrome | Meningioma | Schizotypal Personality Disorder | Abetalipoproteinemia | Camptocormia | Lateral Meningocele Syndrome | Osteogenesis Imperfecta Type III | Cancer, Kidney | Kidney Stones | Walker-Warburg Syndrome | Cholestasis, Intrahepatic | Diabetes Gestational | Gestational Trophoblastic Disease | Holoprosencephaly | Iron Overload | Ellis-Van Creveld Syndrome | Angiosarcoma Of The Breast | Hyperkalemic Periodic Paralysis | Encephalitis | Thromboembolism | Liver Failure, Acute Infantile | Meningeal Melanocytoma | Amelogenesis Imperfecta | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Hidradenitis Suppurativa | Hypohidrotic Ectodermal Dysplasia | Spinocerebellar Ataxia Type 5 | Hypermetropia | Rett Syndrome | Osteopetrosis | Crimean-Congo Hemorrhagic Fever | Hypersomnia | Fibrillation, Atrial | Mitochondrial Encephalomyopathy | Skin Papilloma | Mitochondrial DNA Depletion Syndrome | Benign Familial Infantile Seizures | Tinea Versicolor | Oculocutaneous Albinism Type 1 | Osteopathia Striata With Cranial Sclerosis | Transthyretin-related Amyloidosis | Empyema | Lymphoma, AIDS-related | Lymphopenia | Paget's Disease Of The Breast | Acute Lymphocytic Leukemia | Proteasome-associated Autoinflammatory Syndrome 2 | Batten Disease | Keratitis-ichthyosis-deafness Syndrome | Pemphigus | Arterial Tortuosity Syndrome | Glycogen Storage Disease Type 6 | Riboflavin Transporter Deficiency Neuronopathy | Leiomyoma | Encephalocele | Duane Retraction Syndrome | Acute Kidney Injury | Sepiapterin Reductase Deficiency | Babesiosis | Spinocerebellar Ataxia Type 20 | Lymphangiomatosis | Dyggve-Melchior-Clausen Disease | Fanconi Syndrome | Angiomyolipoma | Intracerebral Hemorrhage | Keratosis, Seborrheic | Sclerosteosis | Antithrombin III Deficiency | Galactosemia | Pyloric Stenosis, Infantile Hypertrophic | Adrenal Insufficiency | Metachromatic Leukodystrophy | Spinocerebellar Ataxia Type 2 | Pneumonia, Mycoplasma | Hennekam Lymphangiectasia-lymphedema Syndrome | Depression | GLUT1 Deficiency Syndrome | Aarskog-Scott Syndrome | Mitochondrial Myopathy | Hypermethioninemia | Peroxisomal Disorder | Uveitis | Neurodegeneration With Brain Iron Accumulation | Keratopathy | Panic Disorder | Peripheral T-cell Lymphoma | Lymphoma, Mantle Cell | Lyme Disease | Leukoplakia, Oral | Nephropathy | Spinocerebellar Ataxia Type 42 | Dental Caries | Spinocerebellar Ataxia Type 21 | Gastroenteritis, Eosinophilic | Pregnancy, Ectopic | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Hepatitis, Chronic | L-2-Hydroxyglutaric Aciduria | Bronchiectasis | Treacher Collins Syndrome | Chronic Granulomatous Disease, X-linked | Dysgerminoma | Parapsoriasis | Adenocarcinoma | Vogt-Koyanagi-Harada Syndrome | Angioedema, Acquired | Argininosuccinic Aciduria | Osteogenesis Imperfecta Type I | Ependymoma | Inflammatory Joint Disease | Tardive Dyskinesia | Fraser Syndrome | Thyroiditis | Cerebral Cavernous Malformations | Chromosome 5q Deletion Syndrome | Cranioectodermal Dysplasia | Meckel-Gruber Syndrome | Retinal Diseases | Mannosidase Deficiency Diseases | Lewy Body Dementia | Systemic Mastocytosis | Antley-Bixler Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Cone Dystrophy | Hypospadias | Arthropathy | Polyneuropathy | Paracoccidioidomycosis