Disease

Endophthalmitis

About the Disease
Endophthalmitis is related to acute endophthalmitis and purulent endophthalmitis, and has symptoms including redness or discharge of eye An important gene associated with Endophthalmitis is CARD9 (Caspase Recruitment Domain Family Member 9), and among its related pathways/superpathways are Innate Immune System and TGF-Beta Pathway. The drugs Cefazolin and Lidocaine have been mentioned in the context of this disorder. Affiliated tissues include eye, endothelial and liver, and related phenotypes are no effect and no effect

Common Targets
CARD9

疾病靶点研报
Endophthalmitis

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

Other Diseases

Usher Syndrome Type IIC | Teratozoospermia | Fetal Alcohol Syndrome | Gilbert Syndrome | Meningeal Melanocytoma | Sengers Syndrome | Thyroid Dyshormonogenesis | Granular Corneal Dystrophy Type 1 | X-linked Acrogigantism | Cousin Syndrome | Hepatitis | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Sarcoma | Asthma | Chronic Lymphocytic Leukemia | Pancytopenia | Pseudohypoparathyroidism Type 1B | Blepharoconjunctivitis | Kearns-Sayre Syndrome | Diverticulitis | Intestinal Tuberculosis | Sotos Syndrome | Larsen Syndrome | Lymphedema | Antithrombin III Deficiency | Birt-Hogg-Dube Syndrome | Malaria, Cerebral | HELLP Syndrome | Pearson Syndrome | Mitochondrial Disease | Pheochromocytoma | Polymyalgia Rheumatica | Infantile Liver Failure Syndrome 1 | T-cell Prolymphocytic Leukemia | Epidermal Nevus Syndrome | ADNP Syndrome | Parkinson's Disease | Crohn's Disease | Swine Influenza | Intracranial Hypertension | Spinocerebellar Ataxia Type 20 | Jalili Syndrome | Diabetic Encephalopathy | Migraine | ICF Syndrome | Crouzon Syndrome With Acanthosis Nigricans | Tuberculous Meningitis | Hypogammaglobulinemia | Optic Nerve Diseases | Liver Diseases | Gyrate Atrophy Of The Choroid And Retina | Primary Carnitine Deficiency | Bronchitis, Chronic | Polycystic Kidney, Autosomal Recessive | Loeys-Dietz Syndrome | Martsolf Syndrome | Marinesco-Sjogren Syndrome | Purpura, Thrombotic Thrombocytopenic | Kabuki Syndrome | Keratopathy | Prolymphocytic Leukemia | Congenital Dyserythropoietic Anemia Type 4 | Zimmermann-Laband Syndrome | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Pulmonary Vein Stenosis | Hereditary Spherocytosis | Vitreoretinal Degeneration, Snowflake Type | Antisocial Personality Disorder | Mitochondrial Cytopathy | Encephalopathy, Glycine | Hyperbilirubinemia | Subacute Sclerosing Panencephalitis | Rosacea | Distal Spinal Muscular Atrophy | Chronic Granulomatous Disease | Frank-ter Haar Syndrome | Melanoma, Uveal | Dermatitis Herpetiformis | Myotonic Disorders | Pigment Dispersion Syndrome | Filariasis | Hypermetropia | Cardiomyopathy, Hypertrophic | Peripheral Neuropathy | Temtamy Preaxial Brachydactyly Syndrome | Emery-Dreifuss Muscular Dystrophy | Poikiloderma With Neutropenia | Juvenile Hyaline Fibromatosis | Hidradenitis | Dementia, Vascular | Congenital Diaphragmatic Hernia | Cancer, Prostate | Harlequin Ichthyosis | Hashimoto Thyroiditis | Pelizaeus-Merzbacher Disease | Frontometaphyseal Dysplasia | Gangliosidosis, GM1 | Stromal Corneal Dystrophy | Acute Motor Axonal Neuropathy | Corneal Dystrophy | Sporadic Hemiplegic Migraine | Primary Familial Brain Calcification | Meniere's Disease | Choriocarcinoma | Myoclonus-dystonia Syndrome | Cardiospondylocarpofacial Syndrome | Brachydactyly | Androgen Insensitivity | Multiple Epiphyseal Dysplasia | Batten Disease | Meier-Gorlin Syndrome | Autosomal Recessive Spastic Paraplegia Type 75 | Hydrolethalus Syndrome | Dystonia Musculorum Deformans | Vertebrobasilar Insufficiency | Vaginitis | Osteoarthritis | Paroxysmal Nocturnal Hemoglobinuria | Blepharo-cheilo-odontic Syndrome | Language Disorders | Milk Allergy | Congenital Heart Defects | Pneumonia, Viral | Salla Disease | Aspartylglycosaminuria | Pemphigus | Osteopathia Striata With Cranial Sclerosis | Vertigo | Congenital Muscular Dystrophy | Lipid Storage Myopathy | Non-epidermolytic Palmoplantar Keratoderma | Epidermolysis Bullosa Acquisita | Cutaneous Mastocytosis | Early Infantile Epileptic Encephalopathy 1 | Familial Male-limited Precocious Puberty | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Mucolipidosis Type III | Lymphoma, AIDS-related | Fowler's Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Wilson's Disease | Chronic Granulomatous Disease, X-linked | Empyema | Neurogenic Bladder | Cyst | Dentinogenesis Imperfecta | Glycogen Storage Disease Type 0 | Ehlers-Danlos Syndrome | Pineoblastoma | Wolfram Syndrome 2 | Amyotrophic Lateral Sclerosis, Juvenile | Autoimmune Polyendocrine Syndrome | Tic Disorder | Hypertriglyceridemia | Cramp Fasciculation Syndrome | Spondylocostal Dysostosis | Tibial Muscular Dystrophy | Long QT Syndrome Type 2 | KBG Syndrome | Chronic Idiopathic Myelofibrosis | Lipodystrophy | Antenatal Bartter Syndrome Type 1 | Diabetes Insipidus, Nephrogenic | Adenomyosis | Cheilitis | Hereditary Sensory Neuropathy Type 1 | Congenital Hemolytic Anemia | Astrocytoma, Anaplastic | Pathological Gambling | Epilepsy, Generalized | Keratocystic Odontogenic Tumor | Amebiasis | Rubeosis Iridis | Wiedemann-Steiner Syndrome | Metabolic Diseases | Werner's Syndrome | Tinea Versicolor | Neutrophilia | Crigler-Najjar Syndrome | AIDS Dementia Complex | Chitayat Syndrome | Recurrent Respiratory Papillomatosis | Adenosine Deaminase Deficiency | Adult Polyglucosan Body Disease | Granular Corneal Dystrophy | Nicotine Addiction | Intestinal Obstruction | Creatine Deficiency Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Citrullinemia | Acanthosis Nigricans | GATA2 Deficiency | Panic Disorder | Periodontitis | Transient Bullous Dermolysis Of The Newborn | Acute Myeloid Leukemia | Spondylocarpotarsal Synostosis Syndrome | Astigmatism | Pupil Disorders | Hepatitis, Alcoholic | Inflammatory Joint Disease | Bulimia Nervosa | Thyroid Dysgenesis | Spondyloperipheral Dysplasia | Porphyria Cutanea Tarda | Narcolepsy | Spinocerebellar Ataxia Type 21 | Spinocerebellar Ataxia Type 15 | Myositis | Encephalitis | Facioscapulohumeral Muscular Dystrophy Type 2 | Diffuse Intrinsic Pontine Glioma | Meesmann Corneal Dystrophy | Inborn Errors Of Metabolism | Still Disease | Gangliosidosis | Renal Failure | Sclerosteosis | AIDS | Pulverulent Zonular Cataract | Seizures | Pneumonia, Bacterial | Snyder-Robinson Syndrome | Poretti-Boltshauser Syndrome | Hemorrhoids | Conduct Disorder | Addison Disease | Peripheral T-cell Lymphoma | Cryopyrin-associated Periodic Syndromes | Acrodysostosis | Tyrosinemia Type 2 | Cardiomyopathy, Peripartum | Keratoconus | Adrenal Insufficiency | Hepatic Adenomatosis | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Hyperparathyroidism, Secondary | Idiopathic Multicentric Castleman Disease | Takotsubo Cardiomyopathy | Niemann-Pick Disease, Type A | C3 Glomerulopathy | Juvenile Polyposis | Granuloma Annulare | VACTERL/VATER Association | Multiple Hamartoma Syndrome | Calcium Pyrophosphate Deposition Disease | Osteopetrosis | Pleomorphic Xanthoastrocytoma | Botulism | Localized Scleroderma | Atelosteogenesis Type 1 | Heterotaxy | Perry Syndrome | Hodgkin Lymphoma | Spinocerebellar Ataxia Type 40 | Rheumatoid Arthritis | Shprintzen-Goldberg Syndrome | Paroxysmal Kinesigenic Dyskinesia | Herpes Simplex Dermatitis | Spinocerebellar Ataxia Type 27 | Venous Insufficiency | Myosin Storage Myopathy | Pseudomyxoma Peritonei | Sarcosinemia | Canavan Disease | Ameloblastoma | Fukuyama Congenital Muscular Dystrophy | Meningioma, Benign | Dementia | Ophthalmia, Sympathetic | Osteonecrosis Of The Jaw | Geleophysic Dysplasia | Osteogenesis Imperfecta Type III | Leukemia | Progressive External Ophthalmoplegia | Sleep Apnea, Central | Hypoparathyroidism | Keratosis, Seborrheic | Neuroleptic Malignant Syndrome | Alazami Syndrome | Barrett Esophagus | Mucolipidosis Type IV | Transcobalamin Deficiency | Congenital Disorders Of Glycosylation | Lymphoma Lymphoblastic | Hyperuricemic Nephropathy, Familial Juvenile | Leukocyte Adhesion Deficiency Type 1 | Tetanus | Mitochondrial Myopathy | Thin Basement Membrane Disease | Vascular Calcification | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Celiac Disease | Myotonia | Temporal Lobe Epilepsy | COACH Syndrome | Sponastrime Dysplasia | Hereditary Neuropathy With Liability To Pressure Palsies | Goiter, Nodular | Olmsted Syndrome | Fibromyalgia | Autoimmune Disease | Sitosterolemia | Ornithine Transcarbamylase Deficiency | Carcinoma, Signet Ring Cell | Anal Fissure | Hyperuricemia | Gerstmann-Straussler-Scheinker Syndrome | Reye Syndrome | Carey-Fineman-Ziter Syndrome | Cerebrovascular Disorders | Syphilis | Tetraplegia | Pure Autonomic Failure | Wolfram Syndrome | Histoplasmosis | Oligodendroglioma | Creatine Deficiency Syndrome Due To AGAT Deficiency | Cystinosis | Best Macular Dystrophy | Familial Hypertrophic Cardiomyopathy | Epithelioid Hemangioma | Hepatitis, Chronic | Lung Diseases | Benign Familial Neonatal Convulsions | Chromosome 5q Deletion Syndrome | Carbohydrate Metabolism Disorders | Myelofibrosis | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Guanidinoacetate Methyltransferase Deficiency | Vitamin A Deficiency | Williams Syndrome | Cysticercosis | Hyperhomocysteinemia | Abetalipoproteinemia | SAPHO Syndrome | Spinocerebellar Ataxia Type 28 | Left Ventricular Noncompaction | Early Infantile Epileptic Encephalopathy 13 | Hepatitis C, Chronic | Pfeiffer Syndrome | GAPO Syndrome | Osteosclerosis | Dermatofibrosarcoma | Castleman Disease | Corneal Dystrophy And Perceptive Deafness | Waardenburg Syndrome Type 2E | Choroideremia | Achromatopsia | Graft-versus-host Disease | Polyomavirus Nephropathy | Systemic Mastocytosis | Carpal Tunnel Syndrome | Keratoconjunctivitis | Ventricular Septal Defect | Muscle Wasting | Atherosclerosis | Omenn Syndrome | Glomerulonephritis, Membranoproliferative | Hypotension, Orthostatic | Enterocolitis, Necrotizing | Tendinitis | Ocular Hypertension | Apert Syndrome | Infectious Diarrhea | Nephrotic Syndrome Type 1 | Gitelman Syndrome | Pneumoconiosis | Paraganglioma, Carotid Body | Vascular Cognitive Impairment | Erdheim-Chester Disease | Chordoid Glioma | Chondroma | Polymyositis | Hypotrichosis | Blepharitis | Bartsocas-Papas Syndrome | Hypertelorism | Renal Hypomagnesemia 3 | Apparent Mineralocorticoid Excess Syndrome | Methemoglobinemia | Diabetic Nephropathy | Myelomeningocele | Brachial Plexus Neuropathy | Vitelliform Macular Dystrophy | Arterial Tortuosity Syndrome | Bethlem Myopathy | Neurodevelopmental Disorders | Thrombosis | Holt-Oram Syndrome | Gastric Atrophy | Microphthalmia, Syndromic 7 | Lichen Sclerosus | Cholelithiasis | Eczema | CEDNIK Syndrome | Gastroenteritis | Early Infantile Epileptic Encephalopathy 4 | Parkinsonism