Disease

Coloboma

About the Disease
Coloboma of Macula, also known as coloboma, is related to papillorenal syndrome and coloboma of optic nerve. An important gene associated with Coloboma of Macula is FZD5 (Frizzled Class Receptor 5), and among its related pathways/superpathways are Ectoderm differentiation and Mesodermal commitment pathway. Affiliated tissues include eye, retina and heart, and related phenotypes are macular coloboma and nervous system

Common Targets
RARA | PUF60 | BMP4 | TWF1 | MAB21L2 | PAX2 | ABI3BP | BMP7 | SALL2 | BMP3 | MIR204 | ABCB6 | LARP4B | STAB2 | PACS1 | PTCH1 | RBP4 | CHD7 | TANC2 | KLHL22 | TFAP2A | LCP1 | RARB | FZD5 | CDON | ACTG1 | CYP1B1 | PPP1R15B | SOX11 | ALDH1A3 | G10413 | KAT2B | CLDN19

疾病靶点研报
Coloboma

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

Other Diseases

Dyslipidemia | Familial Episodic Pain Syndrome | Keratocystic Odontogenic Tumor | Scapuloperoneal Myopathy, X-linked Dominant | Burn-McKeown Syndrome | Enterocolitis, Necrotizing | Onchocerciasis | Psoriasis | Acne | Loeys-Dietz Syndrome | Diabetes Type 1 | Fukuyama Congenital Muscular Dystrophy | Prune Belly Syndrome | Anorectal Fistula | Cardiomyopathy, Hypertrophic | Empyema | Liebenberg Syndrome | Anorectal Malformations | Myocardial Infarction | Dysequilibrium Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Relapsing Polychondritis | Acral Lentiginous Melanoma | Fibronectin Glomerulopathy | Spinal And Bulbar Muscular Atrophy | Epidermolytic Palmoplantar Keratoderma | Nager Acrofacial Dysostosis | Bietti Crystalline Dystrophy | Chorioretinitis | Autoimmune Autonomic Ganglionopathy | Persistent Fetal Circulation | Pleurisy | Juvenile Xanthogranuloma | Arthropathy | Lymphangiomatosis | Takenouchi-Kosaki Syndrome | Dysferlinopathy | Retinopathy, Diabetic | Peeling Skin Syndrome, Acral Type | Osteitis | LEOPARD Syndrome | Narcolepsy | Autism Spectrum Disorders | Retinal Degeneration | Muscle Wasting | Rosacea | Growth Hormone Excess | Charcot-Marie-Tooth Disease Type 4B1 | Lymphoproliferative Disease, X-linked | Long QT Syndrome Type 3 | Hypercholesterolemia | Retinal Vasculitis | Charcot-Marie-Tooth Disease Type 3 | Homocystinuria | Atherosclerosis | Focal Dermal Hypoplasia | Multiple Epiphyseal Dysplasia | Papilloma | FG Syndrome | Pycnodysostosis | Infertility, Male | Ileitis | Sleep Apnea, Obstructive | Paraplegia | Early Infantile Epileptic Encephalopathy 1 | Olmsted Syndrome | Hereditary Folate Malabsorption | Neuromyelitis Optica | Protein S Deficiency | Stromal Corneal Dystrophy | Silver-Russell Syndrome | Membranous Nephropathy | Hepatoblastoma | Papilledema | Idiopathic Multicentric Castleman Disease | Cold Agglutinin Disease | Geleophysic Dysplasia | Diamond-Blackfan Anemia | Charcot-Marie-Tooth Disease, Type 6 | Chondrodysplasia Punctata 1, X-linked Recessive | Withdrawal Syndrome | Kindler Syndrome | Hyperoxaluria | Schnitzler Syndrome | Porphyria, Variegate | T-cell Chronic Lymphocytic Leukemia | Vulvovaginitis | Retinopathy Of Prematurity | Diabetic Encephalopathy | Warsaw Breakage Syndrome | Glycogen Storage Disease Type 5 | Cardiofaciocutaneous Syndrome | Amenorrhea | Endocarditis | Conjunctivitis, Allergic | Congenital Bilateral Absence Of Vas Deferens | Headache | Ectodermal Dysplasia | Pneumonia, Mycoplasma | Postpartum Depression | Vaginitis | IMAGe Syndrome | Charcot-Marie-Tooth Disease Type 2E | Diabetes Type 2 | Non-Hodgkin Lymphoma | Short-chain Acyl-CoA Dehydrogenase Deficiency | Multicentric Carpotarsal Osteolysis Syndrome | Bainbridge-Ropers Syndrome | Hoyeraal-Hreidarsson Syndrome | Mohr-Tranebjaerg Syndrome | Ocular Surface Squamous Neoplasia | Osteogenesis Imperfecta | Pyelonephritis | Craniolenticulosutural Dysplasia | Neurocutaneous Syndromes | Avian Influenza | Temporal Lobe Epilepsy | Choroideremia | Micro Syndrome | Aldosterone Deficiency | Myofibromatosis | Netherton Syndrome | Neuromuscular Disorders | Cancer, Bladder | Epilepsy, Generalized | Shprintzen-Goldberg Syndrome | Bone Marrow Necrosis | Bipolar Disorder | Heart Block | Dementia, Vascular | Cerebellofaciodental Syndrome | Mabry Syndrome | Fibromyalgia | WAGR Syndrome | Epidermolysis Bullosa Dystrophica | Glucagonoma | Arrhythmogenic Right Ventricular Cardiomyopathy | Waardenburg Syndrome | Generalized Epilepsy And Paroxysmal Dyskinesia | Otitis Externa | Eosinophilic Asthma | Kashin-Beck Disease | Pulverulent Zonular Cataract | Esotropia | Hepatitis D | Isobutyryl-CoA Dehydrogenase Deficiency | Uveitis | Blepharo-cheilo-odontic Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Urofacial Syndrome | Nemaline Myopathy 10 | Ameloblastic Carcinoma | Retinitis | Hemorrhage | Kabuki Syndrome | Waardenburg Syndrome Type 4 | Mucolipidosis Type IV | AIDS | Pseudomyxoma Peritonei | Pseudohypoparathyroidism Type 1A | Glomerulonephritis | Nephrosclerosis | Hypercholesterolemia, Familial | Benign Familial Pemphigus | Intestinal Pseudo-obstruction | Congenital Nephrotic Syndrome | Apparent Mineralocorticoid Excess Syndrome | DOCK8 Immunodeficiency Syndrome | Bronchitis | Oculopharyngeal Muscular Dystrophy | Osteogenesis Imperfecta Type III | Lateral Meningocele Syndrome | Whipple's Disease | Open-angle Glaucoma | Myopathy | Antisynthetase Syndrome | Retinitis Pigmentosa | Stroke, Ischemic | Ectopia Lentis, Isolated, Autosomal Recessive | Lymphangioleiomyomatosis | Li-Fraumeni Syndrome | Endometritis | Atrioventricular Septal Defect | Thyroiditis, Autoimmune | Carney Triad | Familial Cerebral Amyloid Angiopathy | Acute Leukemia | Photosensitivity | Peutz-Jeghers Syndrome | Peyronie's Disease | Sickle Cell Disease | Megaloblastic Anemia | Cerebral Cavernous Malformations | Rickets | Sensorineural Hearing Loss | Myotonic Disorders | Fibromuscular Dysplasia | Jacobsen Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Tyrosinemia | POEMS Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Hyperlipidemia, Familial Combined | Inflammatory Joint Disease | Meningeal Melanocytoma | X-linked Acrogigantism | Fucosidosis | Lymphoma, AIDS-related | Lymphoma Lymphoblastic | Liver Failure | Mycosis Fungoides | Polymyalgia Rheumatica | Keratosis, Seborrheic | X-linked Sideroblastic Anemia | Lipoma | Rhabdomyosarcoma | Sotos Syndrome | Chromosome 17q21.31 Deletion Syndrome | Cardiomyopathy, Restrictive | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Episodic Ataxia | Veno-occlusive Disease | Mitochondrial Cytopathy | Cramp Fasciculation Syndrome | Cardiomyopathy, Dilated, 1L | Gangliosidosis, GM1 | Pseudohypoparathyroidism Type 1C | Fetal Akinesia Deformation Sequence | Portal Vein Thrombosis | Spondylocostal Dysostosis | Rothmund-Thomson Syndrome | Glycogen Storage Disease Type 6 | Glycogen Storage Disease Type 4 | Hypoglycemia | Strabismus | Hypothyroidism | Primary Progressive Nonfluent Aphasia | Cataract | Emery-Dreifuss Muscular Dystrophy | Microphthalmia | Mast Cell Leukemia | Stomatitis | Carcinoma, Squamous Cell | Rash | Goiter, Nodular | DNA Ligase IV Deficiency | Multiple Sclerosis | Central Retinal Artery Occlusion | Spinocerebellar Ataxia Type 23 | Bruck Syndrome | Neurocysticercosis | Sengers Syndrome | Canavan Disease | Early Infantile Epileptic Encephalopathy 13 | Ollier Disease | Metabolic Diseases | Leiomyosarcoma | Hodgkin Lymphoma | Twin-to-twin Transfusion Syndrome | Tinea | Nail-Patella Syndrome | HUPRA Syndrome | Schizophrenia | Acrodermatitis Enteropathica | Nasodigitoacoustic Syndrome | Wiskott-Aldrich Syndrome | Asplenia | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Smoldering Myeloma | Bullous Pemphigoid | Hartsfield Syndrome | Obesity, Morbid | Dwarfism | REM Sleep Behavior Disorder | Keratoconus | Spinocerebellar Ataxia Type 14 | Measles | Syphilis | Bardet-Biedl Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Microphthalmia, Syndromic 7 | Robinow Syndrome | Cholangiocarcinoma | Hypospadias | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Neurofibromatosis | Corneal Dystrophies, Hereditary | Adrenal Insufficiency | Cancer, Brain | Facioscapulohumeral Muscular Dystrophy | Alopecia Areata | Hemolytic Anemia | Lissencephaly 2 | Werner's Syndrome | Anemia | Pigment Dispersion Syndrome | Hemolytic Uremic Syndrome | Hydrocephalus, Normal Pressure | Williams Syndrome | Hypoproteinemia, Hypercatabolic | Cystitis | Vitamin D Deficiency | Okihiro Syndrome | Granular Corneal Dystrophy Type 1 | Pterygium | Hepatitis, Alcoholic | Congenital Aniridia | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Blepharoconjunctivitis | Angioedema | Congenital Heart Block | Pulmonary Veno-occlusive Disease | Goldenhar Syndrome | Small Lymphocytic Lymphoma | Torticollis | Thromboembolism | Sick Sinus Syndrome 1 | Colorectal Adenoma | Cushing Syndrome | Epidermodysplasia Verruciformis | Trichuriasis | Haim-Munk Syndrome | Marfan Syndrome | Alopecia | Congenital Generalized Lipodystrophy | Sitosterolemia | Bethlem Myopathy | Amish Infantile Epilepsy Syndrome | Ghosal Syndrome | Sarcomatoid Carcinoma Of The Lung | Progressive External Ophthalmoplegia | HELLP Syndrome | Delirium | Hydrocephalus | Jawad Syndrome | Autonomic Neuropathy | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Priapism | Gaucher Disease | Carbohydrate Metabolism Disorders | Conjunctivitis | Hypodontia | Nephropathy | Primary Carnitine Deficiency | Kaposiform Hemangioendothelioma | Aplasia Cutis Congenita | Arthrogryposis | Centronuclear Myopathy | Congenital Primary Aphakia | Myasthenia | Dengue Hemorrhagic Fever | Fontaine Progeroid Syndrome | Cranioectodermal Dysplasia | Atopy | Schwartz-Jampel-Aberfeld Syndrome | Chronic Leukemia | X-linked Charcot-Marie-Tooth Disease | Renal Failure | Bone Giant Cell Tumor | Infectious Diarrhea | Glutaric Aciduria Type 3 | Anorexia Nervosa | Creutzfeldt-Jakob Disease | Basal Ganglia Disease, Biotin-responsive | Purpura | GLUT1 Deficiency Syndrome | Precocious Puberty | Pseudoachondroplasia | Hyperlipidemia Type V | Ventricular Septal Defect | Neurotoxicity | Multiple Sclerosis, Secondary Progressive | Bladder Exstrophy | Oligoasthenoteratozoospermia | Myopia | Periventricular Leukomalacia | Carpal Tunnel Syndrome | Coffin-Lowry Syndrome | Oligodendroglioma | Von Willebrand Disease | Microcephaly, Seizures, And Developmental Delay | Crouzon Syndrome With Acanthosis Nigricans | Androgenic Alopecia | Myositis, Focal | Chromosome 5q Deletion Syndrome | Camptocormia | Hepatitis, Autoimmune | Pyloric Stenosis, Infantile Hypertrophic | Oculocutaneous Albinism Type 4 | Congenital Bile Acid Synthesis Defect | Osteoglophonic Dysplasia | Hemochromatosis | Glioblastoma | Cystitis, Interstitial | 3-methylglutaconic Aciduria Type IV | Encephalopathy | Charcot-Marie-Tooth Disease Type 4E | Juvenile Hyaline Fibromatosis | Sclerosing Cholangitis