Disease

Panuveitis

About the Disease
Panuveitis, also known as diffuse uveitis, is related to sympathetic ophthalmia and macular retinal edema. An important gene associated with Panuveitis is UACA (Uveal Autoantigen With Coiled-Coil Domains And Ankyrin Repeats), and among its related pathways/superpathways are Cytokine Signaling in Immune system and Innate Immune System. The drugs Adalimumab and Prednisone have been mentioned in the context of this disorder. Affiliated tissues include eye, retina and bone marrow, and related phenotypes are no effect and no effect

Common Targets
DHODH | HLA-DRB1 | G7124 | HLA-DQB1

疾病靶点研报
Panuveitis

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

Other Diseases

Feingold Syndrome | Acne | Gerodermia Osteodysplastica | Nestor-Guillermo Progeria Syndrome | Raine Syndrome | Dysferlinopathy | Lupus Erythematosus | Lymphangioma | Chronic Thromboembolic Pulmonary Hypertension | Congenital Dyserythropoietic Anemia Type 1 | Retinoblastoma | Headache | Transthyretin-related Amyloidosis | Homocystinuria | Anorexia Nervosa | Kearns-Sayre Syndrome | IgA Nephropathy | Ghosal Syndrome | Adenosine Deaminase Deficiency | Distal Myopathy | Spinocerebellar Ataxia Type 13 | Hyperkalemic Periodic Paralysis | Arterial Tortuosity Syndrome | Polymyositis | IMAGe Syndrome | Silver-Russell Syndrome | Rotor Syndrome | Nail-Patella Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Porencephaly | Cardiomyopathy, Dilated, 1L | Anti-glomerular Basement Membrane Disease | Fuchs Dystrophy | Senior-Loken Syndrome | Scleroderma | Alpha-thalassemia Myelodysplasia Syndrome | Lipodystrophy | Antisocial Personality Disorder | VACTERL/VATER Association | Chordoma | Schnyder Crystalline Corneal Dystrophy | Retinitis Pigmentosa 3 | Sialidosis Type I | Aphasia | Vitamin K Deficiency | Aarskog-Scott Syndrome | Diabetes Type 2 | Sleep Apnea, Central | Paracoccidioidomycosis | Isobutyryl-CoA Dehydrogenase Deficiency | Multiple Sclerosis | Leiomyoma | Coenzyme Q10 Deficiency | Loeys-Dietz Syndrome Type 4 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Chondromyxoid Fibroma | Liver Failure | Hyperbilirubinemia, Neonatal | Ichthyosis, X-linked | Bietti Crystalline Dystrophy | Infectious Diarrhea | Rubeosis Iridis | Diabetes | Lymphoma Lymphoblastic | Fundus Albipunctatus | Metatropic Dysplasia | Autoimmune Disease | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Botulism | Alopecia | Amelanotic Melanoma | Priapism | Kaposi Sarcoma | Blau Syndrome | Cleidocranial Dysplasia | Speech Disorders | Rett Syndrome | Necrobiosis Lipoidica | Pseudohypoparathyroidism Type 2 | Nance-Horan Syndrome | Renal Oncocytoma | Oculopharyngeal Muscular Dystrophy | X-linked Sideroblastic Anemia | Nail Disorder, Nonsyndromic Congenital | Meningioma | Tracheal Disorders | Epicondylitis | Congenital Nephrotic Syndrome | Familial Mediterranean Fever | Retinal Vasculitis | Hereditary Spherocytosis | Crimean-Congo Hemorrhagic Fever | Primary Progressive Aphasia | Kleine-Levin Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Myelodysplasia | Epiphyseal Chondrodysplasia, Miura Type | Hemangioblastoma | Aplasia Cutis Congenita | Vogt-Koyanagi-Harada Syndrome | Gardner Syndrome | Gray Platelet Syndrome | Tietze Syndrome | Congenital Bile Acid Synthesis Defect | Schuurs-Hoeijmakers Syndrome | C3 Glomerulopathy | Diffuse Palmoplantar Keratoderma | Cerebellar Ataxia, Cayman Type | Richter's Syndrome | Fibronectin Glomerulopathy | Guillain-Barre Syndrome | Leukemia-lymphoma, Adult T-cell | Endometritis | Arteriovenous Malformations | Angioimmunoblastic T-cell Lymphoma | Spinocerebellar Ataxia Type 20 | Schistosomiasis | Multiple System Atrophy | Wiskott-Aldrich Syndrome | Sotos Syndrome | Scapuloperoneal Spinal Muscular Atrophy | PASLI Disease | Yellow Fever | Rosacea | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Hepatic Steatosis | Vitamin A Deficiency | Familial Male-limited Precocious Puberty | Pineoblastoma | Nager Acrofacial Dysostosis | 5-oxoprolinase Deficiency | Stargardt Disease | Tumoral Calcinosis | Epidermolysis Bullosa Simplex, Localized | CHARGE Syndrome | Poikiloderma With Neutropenia | Myelitis, Transverse | Arthritis, Reactive | Congenital Hypofibrinogenemia | Chronic Myelomonocytic Leukemia | Leiomyosarcoma | X-linked Creatine Transporter Deficiency | Lattice Corneal Dystrophy | Central Core Disease | Malaria, Cerebral | Personality Disorders | Opisthorchiasis | Juvenile Xanthogranuloma | Acrodermatitis | Presbyopia | GAPO Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Astigmatism | Osteopetrosis | Diabetes Type 1 | Lassa Fever | Sengers Syndrome | Charcot-Marie-Tooth Disease Type 4E | Abetalipoproteinemia | Canavan Disease | Trismus-pseudocamptodactyly Syndrome | Primary Hyperoxaluria Type 1 | Osteosarcoma | Carcinoid Tumor | Exocrine Pancreatic Insufficiency | Cystitis | Synovitis | Pituitary Dwarfism | Lymphoma | Diffuse Intrinsic Pontine Glioma | Familial Hypobetalipoproteinemia | Tuberculosis | Situs Inversus | Spinocerebellar Ataxia Type 6 | Prune Belly Syndrome | Muscular Dystrophy | Behavioral Variant Of Frontotemporal Dementia | Nemaline Myopathy 10 | Hypercalciuria | Diverticulitis | Fragile X Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Ichthyosis Hystrix, Curth-Macklin Type | Anovulation | Alopecia Areata | Oguchi Disease-2 | Stomatitis | Hamartoma | Jacobsen Syndrome | Papulopustular Rosacea | Diabetic Encephalopathy | Pigment Dispersion Syndrome | Anterior Segment Dysgenesis | Lafora Disease | Krabbe Disease | Pseudohypoaldosteronism | Impulse Control Disorder | Hartsfield Syndrome | Cole-Carpenter Syndrome | Thrombosis | Neonatal Progeroid Syndrome | Cystinosis | HANAC Syndrome | Coronary Heart Disease | Carcinoma, Merkel Cell | Oculocutaneous Albinism Type 1 | Immunoproliferative Disorders | Retinal Diseases | Motion Sickness | Larsen Syndrome | Acute Tubular Necrosis | Cold Agglutinin Disease | Papillon-Lefevre Syndrome | Anencephaly | Corneal Neovascularization | Pseudoexfoliation Syndrome | Familial Episodic Pain Syndrome | Charcot-Marie-Tooth Disease Type 4 | Alveolar Capillary Dysplasia | Spinocerebellar Ataxia Type 1 | Acanthosis Nigricans | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Non-Hodgkin Lymphoma | Optic Neuropathy, Anterior Ischemic | Schindler Disease | Schaaf-Yang Syndrome | Polymyalgia Rheumatica | Thin Basement Membrane Disease | ICF Syndrome | Chronic Lymphocytic Leukemia | T-cell Leukemia | Paternal Uniparental Disomy Of Chromosome 14 | Mucolipidosis Type III | Persistent Mullerian Duct Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Campomelic Dysplasia | Takayasu's Arteritis | Pilomatrix Carcinoma | Chromosome 8q21.11 Deletion Syndrome | Cryoglobulinemia | Central Retinal Artery Occlusion | 3-methylglutaconic Aciduria | Congenital Central Hypoventilation Syndrome | Oligoastrocytoma | Glomerulonephritis | Danon Disease | Rhabdomyosarcoma, Embryonal | LMNA-related Congenital Muscular Dystrophy | Guanidinoacetate Methyltransferase Deficiency | Mastitis | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Paget's Disease Of The Breast | Primary Torsion Dystonia | Congenital Bilateral Absence Of Vas Deferens | Costello Syndrome | Glutathione Synthetase Deficiency | Pyelonephritis | Congenital Absence Of Vas Deferens | Disseminated Intravascular Coagulation | Tendinopathy | Pulverulent Zonular Cataract | Tay-Sachs Disease | Hypertension, Renovascular | Schizencephaly | Chloridorrhea, Congenital | Localized Scleroderma | Common Cold | Primary Cutaneous Amyloidosis | Neurofibromatosis Type 1 | Hyperammonemia | Sjogren Syndrome | Chromosome 9q34.3 Deletion Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Chudley-McCullough Syndrome | Microphthalmia, Syndromic 7 | Rickets | Ollier Disease | GNE Myopathy | Progressive Familial Intrahepatic Cholestasis Type 1 | Mannosidase Deficiency Diseases | Nephrotic Syndrome Type 1 | Antithrombin III Deficiency | Cutaneous T-cell Lymphoma | Hypohidrotic Ectodermal Dysplasia, X-linked | Alpha-1 Antitrypsin Deficiency | Corneal Dystrophy And Perceptive Deafness | Hypotrichosis Simplex | Fibromyalgia | Congenital Diaphragmatic Hernia | Renal Tubular Dysgenesis | Hartnup Disease | Pearson Syndrome | Keloid | Chondroma | Keratoacanthoma | Hemoglobinopathies | Charcot-Marie-Tooth Disease Type 2E | Meningococcal Meningitis | Netherton Syndrome | Glutaric Aciduria Type 2 | Rheumatic Heart Disease | Cavitary Optic Disc Anomalies | Congenital Heart Defects | Lymphangiomatosis | Juvenile Myelomonocytic Leukemia | Epilepsy Of Infancy With Migrating Focal Seizures | Hashimoto Thyroiditis | Neurofibromatosis | Neurodermatitis | Liver Diseases | Hyperhomocysteinemia | Nicotine Addiction | Carey-Fineman-Ziter Syndrome | Basal Ganglia Disease, Biotin-responsive | Allergic Contact Dermatitis | Polyneuropathy | Dent Disease | Congenital Muscular Dystrophy | Diabetic Neuropathy | Bloom Syndrome | Nephropathy | Primary Pigmented Nodular Adrenocortical Disease | Craniometaphyseal Dysplasia | Ependymoma | Hyperuricemia | Congenital Dyserythropoietic Anemia | Sick Sinus Syndrome | Lymphomatoid Granulomatosis | Androgenic Alopecia | Vascular Cognitive Impairment | Epidermolysis Bullosa | Klippel-Feil Syndrome | Lymphedema | 3-methylglutaconic Aciduria Type I | Amish Infantile Epilepsy Syndrome | Prurigo Nodularis | Pierson Syndrome | Spinocerebellar Ataxia Type 27 | Cat Eye Syndrome | Dysfibrinogenemia | Cardiofaciocutaneous Syndrome | Spinal Cord Diseases | Early Infantile Epileptic Encephalopathy 28 | Blepharospasm | Infertility, Male | Schwannomatosis | Oculocutaneous Albinism Type 4 | Hepatitis | Esophageal Carcinoma | Tibial Muscular Dystrophy | Holt-Oram Syndrome | Klinefelter Syndrome | Intestinal Obstruction | Ectrodactyly | Migraine | NDH Syndrome | Osteogenesis Imperfecta Type IV | Hyperbilirubinemia | Spondylocarpotarsal Synostosis Syndrome | Sleep Apnea | Primary Erythromelalgia | X-linked Myotubular Myopathy | Spinocerebellar Ataxia Type 16 | Prolymphocytic Leukemia | Basal Ganglia Disease | Hyperostosis | Rothmund-Thomson Syndrome | Diastrophic Dysplasia | Goiter | Thanatophoric Dysplasia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Pure Autonomic Failure | Eosinophilic Asthma | Hereditary Xerocytosis | Delirium | Pycnodysostosis | Benign Familial Infantile Seizures | Platelet Disorders | Pemphigoid | Cryptorchidism | Osteonecrosis Of The Jaw | Skin Fragility-woolly Hair Syndrome | Histiocytosis | Leukoplakia, Oral | Cutis Laxa | Ovarian Hyperstimulation Syndrome | Hereditary Coproporphyria | Bulimia Nervosa | Chronic Myeloid Leukemia | Familial Hyperaldosteronism | Renal Tubular Acidosis | HELLP Syndrome | Familial Advanced Sleep Phase Syndrome | Rhinitis | DOCK8 Immunodeficiency Syndrome | Malignant Peripheral Nerve Sheath Tumor | Amelogenesis Imperfecta | Adenomatoid Tumor | Sarcoidosis | Aplastic Anemia