Disease

Bietti Crystalline Dystrophy

About the Disease
Bietti Crystalline Corneoretinal Dystrophy, also known as bietti crystalline dystrophy, is related to scotoma and progressive cone dystrophy. An important gene associated with Bietti Crystalline Corneoretinal Dystrophy is CYP4V2 (Cytochrome P450 Family 4 Subfamily V Member 2), and among its related pathways/superpathways are Fatty acid metabolism and Metapathway biotransformation Phase I and II. Affiliated tissues include eye, retina and skin, and related phenotypes are nyctalopia and constriction of peripheral visual field

Common Targets
CYP4V2

疾病靶点研报
Bietti Crystalline Dystrophy

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

Other Diseases

Tendinopathy | Dwarfism | 3C Syndrome | Meconium Ileus | Infertility | Behcet's Disease | Polycystic Liver | Osteogenesis Imperfecta Type I | Acquired Partial Lipodystrophy | Biotinidase Deficiency | Insulinoma | Hepatitis A | Bronchiolitis | Saul-Wilson Syndrome | X-linked Creatine Transporter Deficiency | Chronic Periodontitis | Congenital Dysfibrinogenemia | Stomatitis | Trichuriasis | Pemphigus | Central Retinal Artery Occlusion | Thanatophoric Dysplasia Type 1 | Lymphoma, Follicular | Schizophrenia, Paranoid | Gastric Atrophy | Gerstmann-Straussler-Scheinker Syndrome | Gray Platelet Syndrome | Bruck Syndrome | Neurotoxicity | Asphyxia Neonatorum | Depression | Antenatal Bartter Syndrome Type 1 | Postpartum Depression | Stevens-Johnson Syndrome | Primary Biliary Cholangitis | Riboflavin Transporter Deficiency Neuronopathy | Hemophagocytic Lymphohistiocytosis | Rhizomelic Chondrodysplasia Punctata | LRBA Deficiency | Pontocerebellar Hypoplasia Type 7 | Diffuse Mesangial Sclerosis | Agranulocytosis | Chondrosarcoma | Irritable Bowel Syndrome | Thrombophlebitis | Liebenberg Syndrome | Bronchitis, Chronic | Palmoplantar Keratoderma | Takotsubo Cardiomyopathy | Crouzon Syndrome With Acanthosis Nigricans | Transthyretin-related Amyloidosis | Distal Spinal Muscular Atrophy | Thyroiditis | Lymphoma | N-acetylglutamate Synthase Deficiency | Anemia | Bone Giant Cell Tumor | Chorea-acanthocytosis | Cryptosporidiosis | Motor Neuron Diseases | Thanatophoric Dysplasia | Neuromuscular Disorders | Vertebrobasilar Insufficiency | Carcinoma, Merkel Cell | Bacterial Meningitis | Kaposi Sarcoma | Antisynthetase Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Rubinstein-Taybi Syndrome | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Rubeosis Iridis | Chronic Mucocutaneous Candidiasis | Hamartoma | Eczema | Stickler Syndrome | Cutaneous Mastocytosis | DICER1 Syndrome | Epidermolytic Palmoplantar Keratoderma | Mannosidase Deficiency Diseases | Nephritis, Interstitial | Cellulitis | Chanarin-Dorfman Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Methylmalonic Acidemia | Glycogen Storage Disease Type 1b | Hairy Cell Leukemia | Porokeratosis | Vitamin A Deficiency | Batten Disease | Fibrillation, Atrial | Tremor | Congenital Tufting Enteropathy | Compartment Syndrome | Pendred Syndrome | Coloboma | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Progressive Familial Intrahepatic Cholestasis | Gingivitis | Tinea | Dysfibrinogenemia | Intestinal Tuberculosis | Primary Hyperoxaluria | Oguchi Disease-2 | Arrhythmogenic Right Ventricular Cardiomyopathy | Netherton Syndrome | Peeling Skin Syndrome Type B | Otopalatodigital Syndrome Type 2 | Myoclonus-dystonia Syndrome | Paget's Disease Of The Breast | Rash | Proximal Symphalangism | Low Phospholipid Associated Cholelithiasis | Endometritis | Maple Syrup Urine Disease | Congenital Dyserythropoietic Anemia Type 4 | Melanoma, Uveal | Spinocerebellar Ataxia Type 6 | Pure Red Cell Aplasia | Clouston Hidrotic Ectodermal Dysplasia | Pyruvate Kinase Deficiency | Ulcerative Colitis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Micro Syndrome | Renal Dysplasia | Gnathodiaphyseal Dysplasia | Speech Disorders | Common Cold | Spinal Muscular Atrophy Type 2 | Mitochondrial Disease | Familial Pheochromocytoma-paraganglioma | Kindler Syndrome | Multiple Sclerosis, Primary Progressive | Dermatomyositis | Cystinosis | Blau Syndrome | Poirier-Bienvenu Neurodevelopmental Syndrome | Liver Failure | Cardiac Sarcoidosis | Tuberculous Meningitis | Ellis-Van Creveld Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Aspergillosis | Fanconi Syndrome | Pontocerebellar Hypoplasia Type 2 | Fragile X Syndrome | Paraplegia | Tricho-hepato-enteric Syndrome | Sertoli Cell-only Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Meckel-Gruber Syndrome | Pycnodysostosis | Periodic Limb Movement Disorder | Brugada Syndrome 1 | Robinow Syndrome | Acral Lentiginous Melanoma | Dysgerminoma | Limb Girdle Muscular Dystrophy | Genee-Wiedemann Syndrome | Liddle Syndrome | Greenberg Dysplasia | Gastroenteritis, Eosinophilic | Dermatofibrosarcoma | HELLP Syndrome | Preaxial Polydactyly | Rheumatoid Arthritis | Pulmonary Alveolar Proteinosis | Pompe Disease | Neurofibrosarcoma | Porphyria, Acute Intermittent | Veno-occlusive Disease | Renal Hypouricemia | Androgenic Alopecia | Systemic Lupus Erythematosus | Persistent Hyperplastic Primary Vitreous | Bicuspid Aortic Valve | Gaucher Disease | Nutrition Disorders | Lymphangiomatosis | Carcinoma In Situ | Johanson-Blizzard Syndrome | Hypoglycemia | Waardenburg Syndrome Type 2E | ICF Syndrome | Adrenoleukodystrophy, X-linked | Tendinitis | Microcephaly | Echinococcosis | Traboulsi Syndrome | Tenosynovial Giant Cell Tumor | Progressive Familial Intrahepatic Cholestasis Type 1 | Cartilage Disorders | Mucolipidosis Type IV | Nicotine Addiction | Lipid Storage Myopathy | Disseminated Superficial Actinic Porokeratosis | Pneumonia, Bacterial | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Parkinson's Disease | Pneumonia, Viral | Papilledema | Lassa Fever | Crohn's Disease | Orthostatic Intolerance | Jacobsen Syndrome | Weill-Marchesani Syndrome | Malignant Fibrous Histiocytoma | Autism Spectrum Disorders | Mast Cell Leukemia | Leprosy | Sleep Apnea | Hypertensive Nephropathy | Non-Hodgkin Lymphoma | Sarcoma | Glycogen Storage Disease Type 1a | Left Ventricular Noncompaction | Juvenile Myelomonocytic Leukemia | Sleep Apnea, Central | Early Infantile Epileptic Encephalopathy 13 | Hepatic Adenomatosis | Congenital Generalized Lipodystrophy | Neurocysticercosis | Blastoma, Pleuropulmonary | Language Disorders | Thyroid Dysgenesis | Dupuytren Disease | Nephronophthisis | Paroxysmal Kinesigenic Dyskinesia | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Cluster Headache | Retinal Vasculitis | Cutaneous Lupus Erythematosus | Torticollis | Avian Influenza | Carney Triad | Acute Myeloid Leukemia | Mitochondrial Myopathy | Carcinoid Syndrome | Autosomal Recessive Congenital Ichthyosis | Usher Syndrome Type II | Multiple Sclerosis, Relapsing-remitting | Neuroleptic Malignant Syndrome | Carey-Fineman-Ziter Syndrome | Menetrier Disease | Uveitis, Anterior | Lactose Intolerance | Neurofibroma, Plexiform | Sarcoma, Ewing | Congenital Heart Block | Dysmorphophobia | Pulmonary Capillary Hemangiomatosis | Arterial Tortuosity Syndrome | Gynecomastia | Martsolf Syndrome | Syndactyly | Scoliosis | Nemaline Myopathy 8 | Autonomic Nervous System Disorders | Erythromelalgia | Supravalvular Aortic Stenosis | Genitopatellar Syndrome | Enterocolitis, Necrotizing | Angina Pectoris | Fraser Syndrome | Lichen Sclerosus | Blepharophimosis Syndrome | Loeys-Dietz Syndrome | Anodontia | Histiocytic Sarcoma | Birt-Hogg-Dube Syndrome | Spinocerebellar Ataxia Type 1 | Sarcoidosis | Blue Rubber Bleb Nevus Syndrome | Tularemia | Hereditary Coproporphyria | Cryptorchidism | Chordoid Glioma | Oligoasthenoteratozoospermia | Hepatitis, Alcoholic | Varices | Epilepsy | Hyperekplexia | Gout | Anencephaly | Mesothelioma, Malignant | Acute Anterior Uveitis | Juvenile Hyaline Fibromatosis | Lymphoma, Mantle Cell | Infertility, Male | Colitis, Collagenous | Gitelman Syndrome | Premenstrual Syndrome | Behavioral Variant Of Frontotemporal Dementia | Hyperprolactinemia | Osteosarcoma | Glycogen Storage Disease Type 3 | Metatropic Dysplasia | Angioedema | Polymyositis | Conn Syndrome | Hepatitis C, Chronic | Oral Lichen Planus | Rothmund-Thomson Syndrome | Macrophage Activation Syndrome | Huntington's Disease | Albinism | Scleroderma | Emery-Dreifuss Muscular Dystrophy | Pantothenate Kinase-associated Neurodegeneration | Hemorrhage | Spitz Nevus | Corneal Edema | Double Outlet Right Ventricle | IMAGe Syndrome | Posterior Polar Cataract | Spinocerebellar Ataxia Type 2 | Neutropenia | Moyamoya Disease | Retinitis | Polycythemia | Tay-Sachs Disease | Conduct Disorder | Localized Scleroderma | Sick Sinus Syndrome | Isobutyryl-CoA Dehydrogenase Deficiency | Progressive External Ophthalmoplegia | Gastritis | Cutaneous T-cell Lymphoma | Asperger Syndrome | Pemphigus Foliaceus | Gestational Trophoblastic Disease | Heart Block | Geleophysic Dysplasia | Scapuloperoneal Myopathy, X-linked Dominant | Primary Hyperoxaluria Type 1 | Constipation | Hypersensitivity Pneumonitis | Cold-induced Sweating Syndrome | Spermatocele | Congenital Hypofibrinogenemia | Macrophagic Myofasciitis | Learning Disability | Erectile Dysfunction | Cardiomyopathy, Dilated, 1L | Gangliosidosis, GM1 | Hemorrhagic Disorders | Myopia | Spinocerebellar Ataxia Type 15 | Congenital Stromal Corneal Dystrophy | Generalized Epilepsy With Febrile Seizures Plus | Osteogenesis Imperfecta | Encephalopathy, Glycine | Iron Metabolism Disorders | 3-methylglutaconic Aciduria | Chitayat Syndrome | Ectrodactyly | Hemochromatosis Type 2 | Neurodermatitis | Synovitis | Spinocerebellar Ataxia Type 8 | Neurofibromatosis-Noonan Syndrome | Polyneuropathy | Globozoospermia | Beckwith-Wiedemann Syndrome | Portal Vein Thrombosis | Conjunctivitis, Allergic | Carpenter Syndrome | Primary Progressive Aphasia | Adenocarcinoma | Chiari Malformation Type I | Dentinogenesis Imperfecta | Pancytopenia | Dysferlinopathy | Leukocyte Adhesion Deficiency Type 1 | Heroin Dependence | Anosmia, Congenital | Trichothiodystrophy | Astrocytoma, Anaplastic | Hemolytic Uremic Syndrome | Progressive Osseous Heteroplasia | MIRAGE Syndrome | Charcot-Marie-Tooth Disease Type 4D | Fabry's Disease | Silver-Russell Syndrome | Esophageal Motility Disorders | Epidermolysis Bullosa Simplex, Localized | Osteoglophonic Dysplasia | Fibronectin Glomerulopathy | Chondrodysplasia Punctata | Spinocerebellar Ataxia Type 21 | Arthropathy | Blepharitis | Optic Nerve Diseases | Hyperparathyroidism-jaw Tumor Syndrome | Anorectal Fistula | Pneumococcal Meningitis | Cole-Carpenter Syndrome | Epidermodysplasia Verruciformis | Spinocerebellar Ataxia Type 14 | Spondylolisthesis | Hypotension, Orthostatic