Disease

Cat Eye Syndrome

About the Disease
Cat Eye Syndrome, also known as ces, is related to cauda equina syndrome and major depressive disorder, and has symptoms including seizures An important gene associated with Cat Eye Syndrome is CECR (Cat Eye Syndrome Chromosome Region). Affiliated tissues include eye, heart and kidney, and related phenotypes are anal atresia and preauricular skin tag

Common Targets
ADA2

疾病靶点研报
Cat Eye Syndrome

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

Other Diseases

Tyrosine Hydroxylase Deficiency | Spondyloperipheral Dysplasia | Premenstrual Syndrome | Mast Cell Leukemia | Parvovirus B19 Infection | Congenital Dysfibrinogenemia | Anal Fissure | Chromosome 17q21.31 Deletion Syndrome | Syncope | Tietze Syndrome | Epidermolysis Bullosa Dystrophica | Autism Spectrum Disorders | Tetraplegia | Mesothelioma, Malignant | Syndactyly | Lattice Corneal Dystrophy | Lamellar Ichthyosis | Chondrodysplasia Punctata 1, X-linked Recessive | Actinomycetoma | Myasthenia Gravis | Microcephalic Primordial Dwarfism | Myelodysplasia | Leukoencephalopathy, Progressive Multifocal | Alveolar Capillary Dysplasia | Epidermal Nevus Syndrome | Impetigo | Lateral Meningocele Syndrome | Chronic Myelomonocytic Leukemia | Chronic Lymphocytic Leukemia | Spinocerebellar Ataxia Type 8 | Gyrate Atrophy Of The Choroid And Retina | Acne Vulgaris | Autoimmune Autonomic Ganglionopathy | Conduct Disorder | Thanatophoric Dysplasia | Familial Dysautonomia | Antithrombin III Deficiency | Chitayat Syndrome | Gaucher Disease | Sclerosteosis | Prolidase Deficiency | Motor Neuron Diseases | Oligoasthenoteratozoospermia | Gangliosidosis | Lipodystrophy | Depression | Autoimmune Polyendocrinopathy Syndrome Type I | Tuberculous Meningitis | Genee-Wiedemann Syndrome | Cataract | Hemoglobinopathies | Familial Hemiplegic Migraine | Microcephaly, Seizures, And Developmental Delay | Gastritis, Atrophic | Nephronophthisis | Neurofibroma | Ectodermal Dysplasia | Coloboma | Panniculitis | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Carcinoma In Situ | Iron Deficiency Anemia | Compartment Syndrome | Schindler Disease | Sjogren Syndrome | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Membranous Nephropathy | Influenza | Maternally Inherited Diabetes And Deafness | Acne | Familial Hypertrophic Cardiomyopathy | Chloridorrhea, Congenital | Wieacker-Wolff Syndrome | Cryptosporidiosis | Inborn Errors Of Metabolism | Hypothalamic Obesity | Cold-induced Sweating Syndrome | Blau Syndrome | Hypoglycemia | Hernia, Inguinal | Headache | Polycythemia Vera | Mumps | Xeroderma Pigmentosum | 3-hydroxy-3-methylglutaric Aciduria | Intestinal Pseudo-obstruction | Kashin-Beck Disease | Craniopharyngioma | Seminoma | Peroxisomal Disorder | Norrie Disease | Intestinal Tuberculosis | Methemoglobinemia | Erysipelas | Neuromuscular Disorders | Splenomegaly | Encephalopathy, Glycine | Malaria | MIRAGE Syndrome | Seborrheic Dermatitis | Cystitis | Nicotine Addiction | Cerebral Amyloid Angiopathy | Cranial Nerve Disease | Oligoastrocytoma | Kallmann Syndrome | Hypocalcemia | Duchenne Muscular Dystrophy | Niemann-Pick Disease, Type C | Agnathia-Otocephaly Complex | Osteopetrosis | Adrenoleukodystrophy, X-linked | Arterial Tortuosity Syndrome | Uremic Pruritus | Smith-Magenis Syndrome | Rhinitis | Takotsubo Cardiomyopathy | Anthrax | Adenocarcinoma | D-2-Hydroxyglutaric Aciduria | Arthritis, Gouty | Chromosome 16p11.2 Deletion Syndrome | MELAS Syndrome | Congenital Adrenal Hyperplasia | Scapuloperoneal Myopathy, X-linked Dominant | Mitochondrial Cytopathy | Scleroderma, Diffuse | Thyroid Dyshormonogenesis | H Syndrome | Osteonecrosis Of The Jaw | Patent Foramen Ovale | Alopecia | Cryopyrin-associated Periodic Syndromes | Immunoproliferative Disorders | Myotonia | Renpenning Syndrome | Neovascular Glaucoma | Fibromuscular Dysplasia | Pancreatitis | Focal Facial Dermal Dysplasia | Dysfibrinogenemia | COACH Syndrome | Cerebrovascular Disorders | Hyperprolactinemia | Acute Motor Axonal Neuropathy | Hemangioma | Thalassemia | Leri Pleonosteosis | Hypotrichosis Simplex | Purpura, Thrombotic Thrombocytopenic | Seizures-scoliosis-macrocephaly Syndrome | Hepatoblastoma | Multiple Myeloma | Botulism | Hypersensitivity | Ovarian Sex Cord-stromal Tumor | Pelvic Inflammatory Disease | Glutaric Aciduria Type 2 | Atopic Dermatitis | Polycystic Ovary Syndrome | Schnyder Crystalline Corneal Dystrophy | Pyoderma Gangrenosum | Okihiro Syndrome | Moyamoya Disease | Carcinoid Tumor | Pernicious Anemia | Mastitis | Antenatal Bartter Syndrome Type 1 | Retinitis Pigmentosa 3 | Schwannoma | Focal Cortical Dysplasia Type 2 | Hypoplastic Left Heart Syndrome | Coffin-Lowry Syndrome | Adams-Oliver Syndrome | Withdrawal Syndrome | TARP Syndrome | GM2-gangliosidosis AB Variant | Epidermolysis Bullosa Acquisita | Hemorrhoids | Sialidosis | Turner's Syndrome | Hypertensive Retinopathy | Niemann-Pick Disease, Type B | Hyperparathyroidism-jaw Tumor Syndrome | Congenital Bile Acid Synthesis Defect | Xeroderma Pigmentosum Variant Type | Adenosine Deaminase 2 Deficiency | Loeys-Dietz Syndrome | Sulfite Oxidase Deficiency | B-cell Chronic Lymphocytic Leukemia | Gastroenteritis | Kidney Stones | Discoid Lupus Erythematosus | Sensorineural Hearing Loss | Hyperbilirubinemia, Neonatal | Cysticercosis | Poirier-Bienvenu Neurodevelopmental Syndrome | Neural Tube Defect | Neutrophilia | VACTERL Association | Non-proliferative Diabetic Retinopathy | Congenital Dyserythropoietic Anemia Type 4 | Mucormycosis | Pericarditis | Progressive Familial Intrahepatic Cholestasis | Atherosclerosis | Spina Bifida | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | X-linked Acrogigantism | Nasodigitoacoustic Syndrome | Amish Infantile Epilepsy Syndrome | Gallstones | Carotid Artery Disease | Cardiomyopathy, Restrictive | Melanoma, Uveal | Hydrolethalus Syndrome | Carcinoma, Signet Ring Cell | Leukoplakia | Schizophrenia | Dowling-Degos Disease | Paracoccidioidomycosis | Trichuriasis | Schwannomatosis | Pituitary Stalk Interruption Syndrome | Papillorenal Syndrome | Low Tension Glaucoma | Cenani-Lenz Syndactyly Syndrome | Familial Cerebral Amyloid Angiopathy | Gingivitis | Neutropenia | Nanophthalmos | Ulcerative Colitis | Palmoplantar Keratoderma | Tatton-Brown-Rahman Syndrome | Milk Allergy | POEMS Syndrome | Malaria, Cerebral | Vitamin A Deficiency | Basan Syndrome | Chylothorax, Congenital | Delayed Sleep Phase Syndrome | Plasma Cell Leukemia | Liebenberg Syndrome | Pantothenate Kinase-associated Neurodegeneration | Amyotrophic Lateral Sclerosis | Saethre-Chotzen Syndrome | Azoospermia | Sclerosing Cholangitis | Congenital Ichthyosiform Erythroderma | Anti-glomerular Basement Membrane Disease | Cancer, Kidney | Cholangitis | Asthma, Exercise-induced | Anencephaly | Carney Triad | Blepharospasm | Hereditary Sensory And Autonomic Neuropathy | Rhabdomyosarcoma | Epidermolytic Ichthyosis, Annular | Fibronectin Glomerulopathy | Low Phospholipid Associated Cholelithiasis | Meniere's Disease | Autosomal Recessive Bestrophinopathy | Postpartum Depression | Precocious Puberty | Congenital Muscular Dystrophy | Urticaria | Leber Hereditary Optic Neuropathy | Epicondylitis | Bernard-Soulier Syndrome | Hemimegalencephaly | Cancer, Colon | Familial Hypobetalipoproteinemia | Cutaneous Angiosarcoma | Parapsoriasis | Optic Neuritis | Peripheral Neuropathy | Lissencephaly 2 | Rift Valley Fever | Spitz Nevus | Generalized Epilepsy With Febrile Seizures Plus | Cancer, Prostate | Infantile Refsum Disease | Bladder Exstrophy | Myositis, Focal | Diamond-Blackfan Anemia | Central Pain Syndrome | Rubinstein-Taybi Syndrome | Arrhythmogenic Right Ventricular Cardiomyopathy | Alzheimer Disease, Late Onset | Encephalocele | Arteriosclerosis | Warsaw Breakage Syndrome | Neurocutaneous Melanocytosis | Charcot-Marie-Tooth Disease Type 4 | Cavitary Optic Disc Anomalies | Peters-plus Syndrome | Heroin Dependence | Christianson Syndrome | Hypokalemic Periodic Paralysis | Iron Metabolism Disorders | Congenital Heart Block | Osteomalacia | Diabetes Insipidus, Neurogenic | Lentigo | Kleine-Levin Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Uveitis, Anterior | Neurofibrosarcoma | Centronuclear Myopathy | Pre-eclampsia | Learning Disability | Hepatitis, Autoimmune | Heterotopic Ossification | Mycosis Fungoides | Fuchs Dystrophy | Strabismus | Ectopia Lentis, Isolated, Autosomal Recessive | N-acetylglutamate Synthase Deficiency | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Oligodendroglioma | Primary Sclerosing Cholangitis | Multicystic Renal Dysplasia | Diarrhea | Homocystinuria | Papulopustular Rosacea | Bursitis | Keratosis | Prune Belly Syndrome | Intracerebral Hemorrhage | Dental Caries | Sitosterolemia | Menetrier Disease | Autoimmune Polyendocrine Syndrome | Granular Corneal Dystrophy | Progressive Encephalopathy-optic Atrophy Syndrome | Cryptococcal Meningitis | Charcot-Marie-Tooth Disease Axonal Type 2N | IgA Nephropathy | Congenital Torticollis | Pouchitis | Encephalitis, Tick-borne | Vaginitis | Varicocele | Tracheal Disorders | Stomatitis | Dengue Shock Syndrome | Congenital Absence Of Vas Deferens | Tylosis With Esophageal Cancer | Combined Malonic And Methylmalonic Acidemia | Cornelia De Lange Syndrome | Corneal Edema | Angiodysplasia | Cancer, Skin | Blastoma, Pleuropulmonary | Hypotrichosis | Tinea | Heavy Chain Disease | Intermittent Claudication | Acrodermatitis Enteropathica | Pneumothorax | Primary Erythromelalgia | Sarcoidosis, Pulmonary | Swine Influenza | Epidermolytic Palmoplantar Keratoderma | Alstrom Syndrome | Paronychia | Hypersomnia | Sensory Neuropathy | Sarcoidosis | Takayasu's Arteritis | Language Disorders | Bacterial Meningitis | Ocular Hypertension | Hepatic Veno-occlusive Disease | Benign Recurrent Intrahepatic Cholestasis 1 | Communication Disorders | Clouston Hidrotic Ectodermal Dysplasia | Alexander Disease | Pancytopenia | Encephalitis | Ovarian Hyperstimulation Syndrome | Stargardt Disease | Globozoospermia | Sotos Syndrome | Cardiomyopathy, Peripartum | Poikiloderma With Neutropenia | Meningococcal Meningitis | Vestibular Disease | Lichen Sclerosus | Inflammatory Bowel Disease | Graves Disease | Esophagitis | Acquired Partial Lipodystrophy | Pituitary Dwarfism | Spinocerebellar Ataxia Type 16 | Congenital Myopathy | Progressive External Ophthalmoplegia | Dermatomyositis | Werner's Syndrome