Congenital Dyserythropoietic Anemia Type 4

About the Disease
Anemia, Congenital Dyserythropoietic, Type Iv, also known as congenital dyserythropoietic anemia type iv, is related to fetal hemoglobin quantitative trait locus 1 and congenital dyserythropoietic anemia. An important gene associated with Anemia, Congenital Dyserythropoietic, Type Iv is KLF1 (KLF Transcription Factor 1). Affiliated tissues include bone marrow, bone and blood and bone marrow, and related phenotypes are frontal bossing and hypothyroidism

Common Targets
KLF1

Note: If you'd like to get a target analysis report for Congenital Dyserythropoietic Anemia Type 4, 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 Congenital Dyserythropoietic Anemia Type 4 at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.

Other Diseases

Heart Failure | Juvenile Polyposis | Apraxia | Tetraplegia | Blomstrand Osteochondrodysplasia | Macular Corneal Dystrophy Type 1 | Arthropathy | HELLP Syndrome | Klinefelter Syndrome | Megaloblastic Anemia | Familial Pheochromocytoma-paraganglioma | Infantile Nephropathic Cystinosis | Sickle Cell Anemia | Bacterial Meningitis | Uremia | Encephalitis | DNA Ligase IV Deficiency | Congenital Adrenal Hyperplasia 1 | Cataplexy | Myeloid Leukemia | Hypospadias | Silicosis | Osteoporosis-pseudoglioma Syndrome | Diabetes Mellitus, Transient Neonatal | Esophageal Carcinoma | Melanoma, Uveal | Sensory Neuropathy | Infantile Spasm | Bethlem Myopathy | Opisthorchiasis | Progressive Familial Intrahepatic Cholestasis Type 3 | Cardiac Sarcoidosis | Leishmaniasis, Cutaneous | Renal Tubular Acidosis | Meningeal Melanocytoma | Lipoma | Hyperthyroidism | Palsy, Cerebral | Leri-Weill Dyschondrosteosis | Silver-Russell Syndrome | Carbamoyl Phosphate Synthetase I Deficiency | Disseminated Intravascular Coagulation | Mitochondrial Cytopathy | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Periodic Limb Movement Disorder | Autoimmune Hemolytic Anemia | Retinal Diseases | Scoliosis | Tyrosinemia Type 1 | Congenital Stationary Night Blindness | Blastoma, Pleuropulmonary | Pierson Syndrome | Hypotonia-cystinuria Syndrome | Malnutrition | Pantothenate Kinase-associated Neurodegeneration | Hydrolethalus Syndrome | Autoimmune Disease | Ectodermal Dysplasia | Torticollis | Spitzoid Melanoma | Hidradenitis | Majeed Syndrome | Tietze Syndrome | Gastroenteritis | Meniere's Disease | Goiter, Nodular | Meningococcal Meningitis | IMAGe Syndrome | Craniofacial Dysostosis | Metaphyseal Chondrodysplasia, Schmid Type | Spasticity | Myasthenia | Nemaline Myopathy 8 | Pulmonary Stenosis | Inborn Errors Of Metabolism | Multifocal Motor Neuropathy | Stuttering | Hepatitis | Seizures | Mastitis | Chronic Leukemia | Juvenile Xanthogranuloma | Esophagitis | Hypoproteinemia, Hypercatabolic | Myoclonus-dystonia Syndrome | Lymphomatoid Granulomatosis | Parapsoriasis | Cancer, Prostate | Bullous Pemphigoid | Familial Cerebral Amyloid Angiopathy | Atrioventricular Septal Defect | Spinocerebellar Ataxia Type 7 | Infectious Diarrhea | Cranioectodermal Dysplasia | Aldosteronism | Hyperammonemia | Pseudohermaphroditism | Vertebrobasilar Insufficiency | Dystonia-parkinsonism, X-linked | Traboulsi Syndrome | Presbycusis | Dermatomyositis | Centronuclear Myopathy | Hereditary Mixed Polyposis Syndrome | Sclerosteosis 2 | Spinocerebellar Ataxia Type 12 | Barrett Esophagus | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Inflammatory Joint Disease | Stiff-man Syndrome | Biotinidase Deficiency | Lissencephaly 2 | Premature Ejaculation | Gynecomastia | Cutis Laxa | Ventricular Septal Defect | Episodic Ataxia | IgA Deficiency | Congenital Heart Block | KBG Syndrome | Hypobetalipoproteinemias | Primary Ovarian Insufficiency | Hyperhomocysteinemia | ACTH-independent Macronodular Adrenal Hyperplasia | Carbohydrate Metabolism Disorders | Carey-Fineman-Ziter Syndrome | Nephrosclerosis | Smith-Kingsmore Syndrome | Pycnodysostosis | Hereditary Multiple Exostoses | Hypertension, Renal | Anti-NMDA Receptor Encephalitis | Uveitis | Aplastic Anemia | Charcot-Marie-Tooth Disease Type 3 | Allan-Herndon-Dudley Syndrome | Nephritis, Interstitial | Gyrate Atrophy Of The Choroid And Retina | Autoimmune Autonomic Ganglionopathy | Rotor Syndrome | Keratocystic Odontogenic Tumor | Hyperprolactinemia | Mosaic Variegated Aneuploidy Syndrome 2 | Purpura | Myhre Syndrome | Gray Platelet Syndrome | Ameloblastic Carcinoma | Cystitis | T-cell Lymphoma, Subcutaneous Panniculitis-like | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Lymphoma, AIDS-related | Light Chain Amyloidosis | Ichthyosis, X-linked | Epithelial-myoepithelial Carcinoma | Filariasis | Central Retinal Artery Occlusion | Jaundice, Obstructive | Tuberculous Meningitis | Farber Disease | Glycogen Storage Disease Type 1 | Urethritis | Kernicterus | Compartment Syndrome | Myotonia | Charcot-Marie-Tooth Disease Axonal Type 2N | Amenorrhea | Hypertelorism | Charcot-Marie-Tooth Disease, Type 2C | Mohr-Tranebjaerg Syndrome | Costello Syndrome | AIDS Dementia Complex | Tularemia | Pneumonia, Bacterial | Sleep Apnea | LRBA Deficiency | Proximal Symphalangism | Borjeson-Forssman-Lehmann Syndrome | Gaucher Disease | Nephroblastoma | Thanatophoric Dysplasia Type 1 | Fucosidosis | Malaria, Cerebral | Progressive External Ophthalmoplegia | Acute Motor Axonal Neuropathy | Prediabetes | Oral Lichen Planus | Hartsfield Syndrome | Spinocerebellar Ataxia Type 5 | Sensorineural Hearing Loss | Optic Nerve Diseases | Hypoalbuminemia | Autism | Macrodactyly | Acromesomelic Dysplasia | Beckwith-Wiedemann Syndrome | Motor Neuron Diseases | Hypercholesterolemia | Lennox-Gastaut Syndrome | Asthma, Nocturnal | Thalassemia | Multiple Sclerosis, Secondary Progressive | Frontometaphyseal Dysplasia | Hypocalcemia | Varices | Congestive Heart Failure | Schamberg Disease | Cole-Carpenter Syndrome | Megalencephaly | Charcot-Marie-Tooth Disease, Type 2 | COACH Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Allergic Contact Dermatitis | Bardet-Biedl Syndrome | Myofibrillar Myopathy | Sarcoma | Cone Dystrophy | Hereditary Spastic Paraplegia | Impetigo | Meningitis | Achromatopsia | Heterotopic Ossification | Pemphigus Foliaceus | Histiocytic Sarcoma | Ectopia Lentis, Isolated, Autosomal Recessive | Osteonecrosis Of The Jaw | Hyperuricemic Nephropathy, Familial Juvenile | Lymphoma, Mantle Cell | Asphyxia Neonatorum | Spinocerebellar Ataxia Type 28 | Metachondromatosis | Tyrosinemia Type 2 | Congenital Nephrotic Syndrome | Dengue Hemorrhagic Fever | Hydrops Fetalis | Pituitary Dwarfism | Myoclonic Atonic Epilepsy | Uremic Pruritus | Coenzyme Q10 Deficiency | Multiple Myeloma | Optic Neuropathy, Anterior Ischemic | Congenital Sodium Diarrhea | Chronic Beryllium Disease | Eosinophilic Asthma | Hemorrhoids | Chorea-acanthocytosis | Chondrodysplasia Punctata 2, X-linked Dominant | Dysmorphophobia | Nijmegen Breakage Syndrome | Thyrotoxic Periodic Paralysis | Methylmalonic Aciduria And Homocystinuria, CblC Type | Agnathia-Otocephaly Complex | Cleidocranial Dysplasia | Rash | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Loeys-Dietz Syndrome | Dystonia Musculorum Deformans | D-2-Hydroxyglutaric Aciduria | Cockayne Syndrome | Atopy | Hypopigmentation | Camurati-Engelmann Disease | Micropenis | Meconium Ileus | Central Pain Syndrome | CEDNIK Syndrome | Patent Foramen Ovale | Maple Syrup Urine Disease | Polyomavirus Nephropathy | Polyradiculopathy | Endometriosis | Chitayat Syndrome | Coronary Artery Disease | Hemophagocytic Lymphohistiocytosis | Chylothorax, Congenital | Nephrotic Syndrome Type 1 | Infertility | Angioimmunoblastic T-cell Lymphoma | Congenital Hemolytic Anemia | Retinitis | Hypolipoproteinemia | Gerstmann-Straussler-Scheinker Syndrome | Fukuyama Congenital Muscular Dystrophy | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Cancer, Brain | Hereditary Coproporphyria | Craniometaphyseal Dysplasia | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Congenital Bilateral Absence Of Vas Deferens | Glutaric Aciduria Type 1 | Twin-to-twin Transfusion Syndrome | Cerebellofaciodental Syndrome | Congenital Heart Defects | Ileitis | Thrombosis | Leri Pleonosteosis | Ichthyosis Hystrix, Curth-Macklin Type | Apert Syndrome | Gitelman Syndrome | Thrombophlebitis | Dementia, Vascular | Pulmonary Capillary Hemangiomatosis | Fibrodysplasia Ossificans Progressiva | Endometritis | Salla Disease | X-linked Sideroblastic Anemia | Hodgkin Lymphoma | Lymphangioma | Bronchiectasis | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Bare Lymphocyte Syndrome | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Familial Digital Arthropathy-brachydactyly | Cavitary Optic Disc Anomalies | Intracerebral Hemorrhage | Castleman Disease | Hypertensive Retinopathy | Wolfram Syndrome | Microcephalic Primordial Dwarfism | Episodic Ataxia Type 2 | Autoimmune Polyendocrinopathy Syndrome Type I | Sarcoma, Alveolar Soft Part | Panniculitis | Myosin Storage Myopathy | Glycogen Storage Disease Type 0, Muscle | Vitelliform Macular Dystrophy | Niemann-Pick Disease, Type B | Whipple's Disease | Babesiosis | Keratoconus | Protein S Deficiency | Lung Diseases | Cystitis, Interstitial | Melanocytic Nevus | Encephalocele | Rickets | Dupuytren Disease | Myelitis, Transverse | Familial Hyperaldosteronism | Hemangioblastoma | Familial Episodic Pain Syndrome | Neurogenic Bladder | Infantile Refsum Disease | Lafora Disease | Combined Malonic And Methylmalonic Acidemia | Ocular Albinism Type 1 | Pain | Glutathione Synthetase Deficiency | Bronchitis, Chronic | Large Granular Lymphocytic Leukemia | Papilledema | Alstrom Syndrome | Peters-plus Syndrome | Vitamin D Deficiency | Thyroid Dyshormonogenesis | Fraser Syndrome | Hartnup Disease | DEND Syndrome | Meningioma | Pontocerebellar Hypoplasia Type 7 | Tylosis With Esophageal Cancer | Hyperphenylalaninemia | Thrombasthenia | Christianson Syndrome | Adams-Oliver Syndrome | Autosomal Recessive Congenital Ichthyosis | Adrenal Insufficiency | Fascioliasis | Acute Generalized Exanthematous Pustulosis | Familial Exudative Vitreoretinopathy | Beare-Stevenson Syndrome | Spinocerebellar Ataxia Type 27 | Neurocutaneous Melanocytosis | Rhabdomyosarcoma, Alveolar | Impulse Control Disorder | Obesity | Retinal Vasculitis | Sialoadenitis | Mood Disorder | Postpartum Depression | NGLY1 Deficiency | Noonan Syndrome-like Disorder With Loose Anagen Hair | Thrombotic Microangiopathy | Paroxysmal Kinesigenic Dyskinesia | AIDS | Pemphigus Vulgaris | Fanconi Anemia | Hyperinsulinemic Hypoglycemia | ICF Syndrome | X-linked Acrogigantism | Carney Triad | Multiple Sulfatase Deficiency | Carcinoid Syndrome | Tonsillitis | Postpoliomyelitis Syndrome | 3C Syndrome | Neuronal Ceroid Lipofuscinosis | Pyruvate Decarboxylase Deficiency | Sponastrime Dysplasia | Lichen Sclerosus | Fibrosis