Disease

Choroideremia

About the Disease
Choroideremia, also known as chm, is related to peripheral retinal degeneration and retinitis. An important gene associated with Choroideremia is CHM (CHM Rab Escort Protein), and among its related pathways/superpathways are Metabolism of proteins and Vesicle-mediated transport. The drugs Simvastatin and Lipid Regulating Agents have been mentioned in the context of this disorder. Affiliated tissues include eye, retina and bone, and related phenotypes are abnormality of retinal pigmentation and abnormal electroretinogram

Common Targets
DNTTIP2 | CHM | PCDH11X | CPXCR1 | MPZ | PABPC5 | LTBP2 | DACH2 | RPE65 | KLHL4

疾病靶点研报
Choroideremia

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

Other Diseases

Diffuse Palmoplantar Keratoderma | Myelitis | Peeling Skin Syndrome Type B | Birk-Barel Syndrome | Incontinentia Pigmenti | Pleurisy | McKusick Type Metaphyseal Chondrodysplasia | Jalili Syndrome | Arthritis, Psoriatic | Borderline Personality Disorder | Scapuloperoneal Myopathy, X-linked Dominant | Histiocytic Sarcoma | Von Willebrand Disease | D-2-Hydroxyglutaric Aciduria | Cat Eye Syndrome | Myopathy | Hepatitis B, Chronic | Borjeson-Forssman-Lehmann Syndrome | Hypoplastic Left Heart Syndrome | Cluster Headache | Crohn's Disease | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Lentigo | Rickets | Hyperbilirubinemia, Neonatal | Duodenal Atresia | Antenatal Bartter Syndrome Type 1 | Focal Segmental Glomerulosclerosis | Cheilitis | Myoclonic Atonic Epilepsy | Basal Cell Nevus Syndrome | Dysplastic Nevus | Fuchs Heterochromic Iridocyclitis | Primary Progressive Nonfluent Aphasia | Leprosy | Coronary Heart Disease | Polycythemia | Xeroderma Pigmentosum | Hemochromatosis Type 1 | Microcephalic Primordial Dwarfism | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Periodic Limb Movement Disorder | Dystrophy, Cone-rod | Mucormycosis | Adenocarcinoma | Richter's Syndrome | Muir-Torre Syndrome | IgA Deficiency | Progressive Familial Intrahepatic Cholestasis Type 3 | Pouchitis | Intestinal Pseudo-obstruction | Meningococcal Infections | Central Pain Syndrome | Papillon-Lefevre Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Hepatic Adenomatosis | X-linked Myotubular Myopathy | Multiple Myeloma | Carpenter Syndrome | Macular Corneal Dystrophy | Myoclonus-dystonia Syndrome | Hyperandrogenemia | Schistosomiasis Mansoni | Hemorrhagic Disorders | Autosomal Recessive Bestrophinopathy | Neurodermatitis | Lateral Meningocele Syndrome | Pyruvate Decarboxylase Deficiency | Autoimmune Hemolytic Anemia | Anemia | Neurocutaneous Melanocytosis | Situs Inversus | Prostatitis | Hereditary Multiple Exostoses | Vasculitis | Charcot-Marie-Tooth Disease Type 4B1 | Leber Hereditary Optic Neuropathy | Osteogenesis Imperfecta Type VI | Myoclonus | Malignant Peripheral Nerve Sheath Tumor | Metabolic Syndrome | Cutaneous T-cell Lymphoma | Giant Cell Arteritis | Diabetes Gestational | Fetal Akinesia Deformation Sequence | Pontocerebellar Hypoplasia Type 7 | Chediak-Higashi Syndrome | Spinocerebellar Ataxia Type 42 | Esophageal Motility Disorders | Lipodystrophy | Hypercalcemia | Stickler Syndrome | Desbuquois Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Tuberculosis | Generalized Epilepsy With Febrile Seizures Plus | Noonan Syndrome-like Disorder With Loose Anagen Hair | Acute Leukemia | Impulse Control Disorder | Perivascular Epithelioid Cell Tumor | Bartter Syndrome | Bethlem Myopathy | Multicentric Carpotarsal Osteolysis Syndrome | Isovaleric Acidemia | Cousin Syndrome | Menetrier Disease | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Hypophosphatasia | Zimmermann-Laband Syndrome | Early Infantile Epileptic Encephalopathy 13 | Torticollis | Non-Hodgkin Lymphoma | Renal-hepatic-pancreatic Dysplasia | Erythropoietic Protoporphyria | Diabetes Insipidus, Nephrogenic | Peripheral T-cell Lymphoma | Polymyositis | Lysosomal Acid Lipase Deficiency | Sleep Disorder | Nemaline Myopathy 10 | Membranous Nephropathy | Paraganglioma | Hyperacusis | Ichthyosis Hystrix, Curth-Macklin Type | Scabies | Chronic Granulomatous Disease | Multiple Sclerosis, Relapsing-remitting | Fibrosis | Microphthalmia | Cardiac Sarcoidosis | Adenylosuccinate Lyase Deficiency | Hashimoto Thyroiditis | Primary Hyperoxaluria Type 3 | Dengue Hemorrhagic Fever | Ameloblastoma | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Carcinoma, Small Cell | Lipid Metabolism Disorders | Androgenic Alopecia | Gerstmann-Straussler-Scheinker Syndrome | Myotonia | DICER1 Syndrome | Pancreatitis, Chronic | Kidney Stones | Cannabis Abuse | Wilson's Disease | Glanzmann Thrombasthenia | Axenfeld-Rieger Syndrome | Familial Mediterranean Fever | Multisystemic Smooth Muscle Dysfunction Syndrome | Myocarditis | Williams Syndrome | Choroideremia | Benign Familial Neonatal Convulsions | Colitis, Lymphocytic | Skin Fragility-woolly Hair Syndrome | Pure Red Cell Aplasia | Ovarian Sex Cord-stromal Tumor | Amenorrhea | 3-hydroxy-3-methylglutaric Aciduria | Mevalonate Kinase Deficiency | Extramammary Paget's Disease | Primary Pigmented Nodular Adrenocortical Disease | Osteoporosis | Chronic Mucocutaneous Candidiasis | Osteochondrosis | Acral Lentiginous Melanoma | Keratosis, Seborrheic | Spinocerebellar Ataxia Type 21 | Lymphoma, Follicular | Language Disorders | Heterotaxy | Atelosteogenesis Type 1 | Atrial Septal Defect | Chanarin-Dorfman Syndrome | Cramp Fasciculation Syndrome | Fibrillation, Atrial | Mixed Connective Tissue Disease | Conduct Disorder | Pompe Disease | Lassa Fever | Epithelioid Hemangioma | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Dubin-Johnson Syndrome | Gastroschisis | Chordoma | Hyperkeratosis | Cholelithiasis | Inflammatory Myofibroblastic Tumor | Hernia, Inguinal | Epidermolytic Palmoplantar Keratoderma | Ichthyosis | Mountain Sickness | NDH Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Nager Acrofacial Dysostosis | Hyperparathyroidism | Lymphangioma | Retinal Dystrophy | Kaposiform Hemangioendothelioma | Christianson Syndrome | Alpers Syndrome | Weill-Marchesani Syndrome | Pure Autonomic Failure | Inflammatory Joint Disease | Atopy | Acute Coronary Syndrome | Lymphopenia | Van Der Knaap Disease | Coffin-Lowry Syndrome | Congenital Dyserythropoietic Anemia Type 4 | Apraxia | Wolcott-Rallison Syndrome | Cholera | Proctitis | Spastic Paraplegia Type 7 | Tangier Disease | Anencephaly | Hepatic Veno-occlusive Disease | Angioedema, Hereditary | CREST Syndrome | Microvillus Inclusion Disease | Abetalipoproteinemia | Meleda Disease | Chronic Enteropathy Associated With SLCO2A1 Gene | Growth Hormone Excess | Pilomatrix Carcinoma | Polydactyly | Tyrosine Hydroxylase Deficiency | Marfan Syndrome | Psoriasis | Hemorrhoids | Bone Giant Cell Tumor | Familial Hypertrophic Cardiomyopathy | Charcot-Marie-Tooth Disease, Type 1A | Lathosterolosis | Chromosome 8q21.11 Deletion Syndrome | Juvenile Polyposis | Tenosynovial Giant Cell Tumor | Hyperinsulinemic Hypoglycemia | Autonomic Nervous System Disorders | Cardiac Arrest | Corneal Edema | Pycnodysostosis | Inflammatory Linear Verrucous Epidermal Nevus | Milk Allergy | Cenani-Lenz Syndactyly Syndrome | CEDNIK Syndrome | VEXAS Syndrome | Myeloid Leukemia | Juvenile Xanthogranuloma | Hyperferritinemia-cataract Syndrome | Fuchs Dystrophy | Mast Cell Leukemia | Galactosialidosis | Ocular Surface Squamous Neoplasia | Pulmonary Sclerosing Hemangioma | Pain | Juvenile Myelomonocytic Leukemia | Rash | Acute Myeloid Leukemia | Combined Pituitary Hormone Deficiency | Molybdenum Cofactor Deficiency | Scapuloperoneal Spinal Muscular Atrophy | Charcot-Marie-Tooth Disease Type 2T | Congenital Sodium Diarrhea | Glycogen Storage Disease Type 5 | Alazami Syndrome | Leigh Syndrome | Amelogenesis Imperfecta | Primary Hyperoxaluria Type 1 | Avellino Corneal Dystrophy | Cholecystitis | Blepharoconjunctivitis | Nestor-Guillermo Progeria Syndrome | Chronic Myeloid Leukemia | Skin Papilloma | Autosomal Recessive Spastic Paraplegia Type 35 | Thyroid Dysgenesis | Oculocutaneous Albinism Type 2 | CHOPS Syndrome | Osteoarthritis | Facioscapulohumeral Muscular Dystrophy Type 2 | Pneumococcal Meningitis | Cryptorchidism | Hereditary Sensory And Autonomic Neuropathy | Pseudohypoparathyroidism Type 1C | Amish Infantile Epilepsy Syndrome | Johanson-Blizzard Syndrome | Thrombophlebitis | Avian Influenza | Cholangitis | Persistent Truncus Arteriosus | 3-methylglutaconic Aciduria Type I | Cirrhosis | Agranulocytosis | Hypertrophy | Neurofibrosarcoma | Cardiomyopathy, Dilated, 1L | Apparent Mineralocorticoid Excess Syndrome | Reye Syndrome | Renal Oncocytoma | Charcot-Marie-Tooth Disease, Type 2 | Congenital Absence Of Vas Deferens | Tinea | Tuberculous Meningitis | Lamellar Ichthyosis | Low Phospholipid Associated Cholelithiasis | Blastoma, Pleuropulmonary | Gyrate Atrophy Of The Choroid And Retina | Macrodactyly | Sotos Syndrome | Nephronophthisis | Woodhouse-Sakati Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Ichthyosis Bullosa Of Siemens | Aplastic Anemia | Diastrophic Dysplasia | Dysmorphophobia | Seborrheic Dermatitis | Myasthenia | Erythematotelangiectatic Rosacea | Chronic Lymphocytic Leukemia | Episodic Ataxia Type 2 | Glaucomatocyclitic Crisis | Glomerulonephritis | Spina Bifida | Gynecomastia | Vogt-Koyanagi-Harada Syndrome | Pineoblastoma | Wiskott-Aldrich Syndrome | Microphthalmia, Syndromic 7 | Intracerebral Hemorrhage | Spinocerebellar Ataxia Type 1 | Episodic Ataxia Type 1 | Dyskeratosis Congenita | Hypercholesterolemia | Hereditary Sensory Neuropathy Type 1 | Thrombosis | Idiopathic Pulmonary Fibrosis | Auriculocondylar Syndrome | Benign Hereditary Chorea | Vitamin B12 Deficiency | Renal Hypomagnesemia 3 | Gangliosidosis, GM1 | Uremic Pruritus | Bietti Crystalline Dystrophy | Blepharitis | Pierson Syndrome | Transthyretin-related Amyloidosis | Thalassemia, Beta | DRESS Syndrome | Warsaw Breakage Syndrome | Klippel-Feil Syndrome | Erythrokeratodermia Variabilis | Behavioral Variant Of Frontotemporal Dementia | Metachondromatosis | Long QT Syndrome Type 3 | Lipid Storage Myopathy | Joubert Syndrome | Strabismus | Ectopia Lentis, Isolated, Autosomal Recessive | Goiter, Nodular | Syphilis | Alpha-thalassemia Myelodysplasia Syndrome | Takotsubo Cardiomyopathy | Hypervalinemia | Craniofrontonasal Syndrome | Imerslund-Grasbeck Syndrome | Temtamy Preaxial Brachydactyly Syndrome | Esophagitis | Waardenburg Syndrome Type 2E | Antiphospholipid Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Sarcoma, Alveolar Soft Part | Glioblastoma Multiforme | Hyperoxaluria | Fibromyalgia | Superficial Spreading Melanoma | Noonan Syndrome | Bartsocas-Papas Syndrome | Graves Disease | Absence Epilepsy | Gangliosidosis | Retinal Coloboma | Spinocerebellar Ataxia Type 7 | Schindler Disease | Acute Tubular Necrosis | Duane Retraction Syndrome | Spinocerebellar Ataxia Type 14 | Jaundice, Obstructive | Cyst | Diabetes Mellitus, Transient Neonatal | Oculocutaneous Albinism Type 4 | Histoplasmosis | Keratocystic Odontogenic Tumor | Pneumoconiosis | Anorectal Malformations | Nance-Horan Syndrome | Polyradiculopathy