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.ai.

Other Diseases

Cholestasis | Fontaine Progeroid Syndrome | Neuropathy | Paroxysmal Nocturnal Hemoglobinuria | Sensory Neuropathy | Neurofibrosarcoma | Haim-Munk Syndrome | Leukemia | Spinocerebellar Ataxia | Binge Eating Disorder | Epithelioid Hemangioma | Spinocerebellar Ataxia Type 20 | Chronic Kidney Disease | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Spinocerebellar Ataxia Type 8 | Autosomal Recessive Spastic Paraplegia Type 35 | Hydrops Fetalis | Fibrosis | Tatton-Brown-Rahman Syndrome | Sweet Syndrome | Pulmonary Tuberculosis | Epiphyseal Chondrodysplasia, Miura Type | Osteoporosis | Varicocele | Carotid Artery Disease | Pre-eclampsia | Kabuki Syndrome 2 | Myotonia | Low Phospholipid Associated Cholelithiasis | Cornelia De Lange Syndrome | Schizophrenia | Frank-ter Haar Syndrome | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Carpal Tunnel Syndrome | Loeys-Dietz Syndrome Type 4 | Meesmann Corneal Dystrophy | Carbohydrate Metabolism Disorders | Nijmegen Breakage Syndrome | Dementia | Blomstrand Osteochondrodysplasia | Corneal Dystrophy And Perceptive Deafness | Emery-Dreifuss Muscular Dystrophy | Pierpont Syndrome | Gnathodiaphyseal Dysplasia | Postpoliomyelitis Syndrome | Combined Pituitary Hormone Deficiency | Glutathione Synthetase Deficiency | Congenital Bile Acid Synthesis Defect | Hypogonadism | Stevens-Johnson Syndrome | Spinocerebellar Ataxia Type 16 | Glucagonoma | Van Der Knaap Disease | Autism Spectrum Disorders | Hyperekplexia | Charcot-Marie-Tooth Disease Axonal Type 2N | Charcot-Marie-Tooth Disease Type 4B1 | Nevus | Subacute Sclerosing Panencephalitis | Atelosteogenesis Type 2 | Diabetes Mellitus, Transient Neonatal | Hemochromatosis Type 2 | Epidermolysis Bullosa Simplex, Generalized | Addison Disease | Waardenburg Syndrome Type 2E | Disseminated Superficial Actinic Porokeratosis | Chorea | Huntington's Disease | Becker Muscular Dystrophy | Brooke-Spiegler Syndrome | Actinomycetoma | Fundus Albipunctatus | Hermansky-Pudlak Syndrome | Congenital Absence Of Vas Deferens | Proopiomelanocortin Deficiency | Roberts Syndrome | Thyroid Dysgenesis | Leukoencephalopathy, Progressive Multifocal | Spina Bifida | Aneurysm, Abdominal Aortic | Meier-Gorlin Syndrome | Pain | Achondrogenesis | Sandhoff Disease | Charcot-Marie-Tooth Disease, Type 1A | Multiple Sclerosis, Secondary Progressive | Angiosarcoma Of The Breast | Lassa Fever | Tylosis With Esophageal Cancer | Arthrogryposis | T-cell Leukemia | Lactose Intolerance | Nemaline Myopathy 10 | Walker-Warburg Syndrome | Guttate Psoriasis | Omenn Syndrome | Huntington's Disease-like 2 | 3-methylglutaconic Aciduria | 3-hydroxy-3-methylglutaric Aciduria | Alopecia Totalis | Aldosteronism | Turner's Syndrome | Meconium Ileus | Necrobiosis Lipoidica | Guillain-Barre Syndrome | Congenital Fiber-type Disproportion Myopathy | Onchocerciasis | Botulism | Mitochondrial Cytopathy | Ophthalmia, Sympathetic | Pseudoachondroplasia | Pneumonia, Viral | Osteomalacia | Hepatic Veno-occlusive Disease | Glaucoma, Congenital | Multicystic Renal Dysplasia | Citrullinemia | Leber Hereditary Optic Neuropathy | DICER1 Syndrome | Woodhouse-Sakati Syndrome | Mucormycosis | Lateral Meningocele Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | Jalili Syndrome | Carcinoma, Small Cell | Sickle Cell Disease | Benign Familial Infantile Seizures | Hypoplastic Left Heart Syndrome | Asthma, Nocturnal | 3C Syndrome | GM2-gangliosidosis AB Variant | Pseudohermaphroditism | Osteomyelitis | Vasculitis | Cellulitis | Schnitzler Syndrome | Corneal Dystrophies, Hereditary | Non-Langerhans Cell Histiocytosis | Lipid Storage Myopathy | Adenylosuccinate Lyase Deficiency | Leukocyte Adhesion Deficiency | Spinocerebellar Ataxia Type 1 | Glycogen Storage Disease Type 5 | Ureteropelvic Junction Obstruction | Alpha-mannosidosis | Migraine | Megalencephaly | Coffin-Lowry Syndrome | Phenylketonuria | Acute Anterior Uveitis | Cirrhosis | Pemphigoid | Hypercalciuria | Malignant Fibrous Histiocytoma | Hyperphenylalaninemia | Budd-Chiari Syndrome | Schistosomiasis Mansoni | Cutis Laxa | Chronic Neutrophilic Leukemia | Liver Failure | Schamberg Disease | Familial Advanced Sleep Phase Syndrome | Martsolf Syndrome | Myotonic Disorders | Fanconi Syndrome | Congenital Primary Aphakia | Periventricular Nodular Heterotopia | Cerebellofaciodental Syndrome | Hodgkin Lymphoma | Opisthorchiasis | Oligoasthenoteratozoospermia | Pancytopenia | Contact Dermatitis | Leukemia-lymphoma, Adult T-cell | Bruck Syndrome | Sepiapterin Reductase Deficiency | Follicular Dendritic Cell Sarcoma | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Chronic Mucocutaneous Candidiasis | Colon Adenoma | Papilloma | Usher Syndrome Type I | Juvenile Polyposis | Paraganglioma, Carotid Body | Waldenstrom Macroglobulinemia | Temtamy Preaxial Brachydactyly Syndrome | Trismus-pseudocamptodactyly Syndrome | Ectrodactyly | Primary Torsion Dystonia | Immunoproliferative Disorders | Malonyl-CoA Decarboxylase Deficiency | Cyst | Colorectal Adenoma | Syncope | Uterine Leiomyoma | Parkinson's Disease | Lymphomatoid Granulomatosis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Hemimegalencephaly | Carcinoma, Squamous Cell | Hyperparathyroidism | Low Tension Glaucoma | Autoimmune Disease | Oral Lichen Planus | Malnutrition | Cholera | Sick Sinus Syndrome | Hemolytic Uremic Syndrome | Uremia | Neurofibroma | Episodic Ataxia Type 2 | Hypertension, Renovascular | Pituitary Stalk Interruption Syndrome | Hypoglycemia | Encephalitis, Tick-borne | Myoclonus-dystonia Syndrome | Azoospermia | Smith-Magenis Syndrome | Juvenile Xanthogranuloma | Preaxial Polydactyly | Colitis, Collagenous | Gallstones | Tuberculosis | Cardiac Arrest | Influenza | Borjeson-Forssman-Lehmann Syndrome | Schuurs-Hoeijmakers Syndrome | Peeling Skin Syndrome, Acral Type | Trichomegaly | Pitt-Hopkins Syndrome | Anorchia | Osteoporosis-pseudoglioma Syndrome | Papillon-Lefevre Syndrome | Dysgerminoma | Pendred Syndrome | Primary Hyperoxaluria Type 1 | Purpura, Thrombotic Thrombocytopenic | Tumoral Calcinosis | Mabry Syndrome | Babesiosis | Ghosal Syndrome | Adenosine Deaminase 2 Deficiency | Paronychia | Melanoma | Eosinophilia | Raine Syndrome | Pelizaeus-Merzbacher Disease | Charcot-Marie-Tooth Disease, Type 2 | Long QT Syndrome Type 1 | Niemann-Pick Disease, Type B | Pycnodysostosis | Keratosis | Scabies | Long QT Syndrome Type 3 | Mosaic Variegated Aneuploidy Syndrome 2 | Avellino Corneal Dystrophy | Agammaglobulinemia | Pneumothorax | Esophagitis | Holt-Oram Syndrome | Chondrodysplasia Punctata 2, X-linked Dominant | Ataxia-ocular Apraxia 2 | Conjunctivitis | Micro Syndrome | Aneurysm, Thoracic Aortic | Depression | Rothmund-Thomson Syndrome | Polymicrogyria | Rift Valley Fever | Rhabdomyosarcoma | Intracerebral Hemorrhage | Personality Disorders | Cardiac Sarcoidosis | Hypertelorism | Galactosemia | C3 Glomerulopathy | Cramp Fasciculation Syndrome | Currarino Syndrome | Zygomycosis | Hyperparathyroidism-jaw Tumor Syndrome | Proximal Symphalangism | Hemochromatosis | Mycosis Fungoides | Dwarfism | Polymyalgia Rheumatica | Traboulsi Syndrome | Trigonocephaly | Gingivitis | Carcinoid Tumor | Gastrointestinal Disorders | Oculocutaneous Albinism Type 1 | Combined Malonic And Methylmalonic Acidemia | Smith-Lemli-Opitz Syndrome | Familial Partial Lipodystrophy | Meningioma, Benign | Nephritis, Interstitial | Erysipelas | Porphyria, Acute Intermittent | Leukoplakia | Dyslipidemia | Prolymphocytic Leukemia | Schaaf-Yang Syndrome | Crimean-Congo Hemorrhagic Fever | Chromosome 17q21.31 Deletion Syndrome | Juvenile Hyaline Fibromatosis | Metatropic Dysplasia | Distal Myopathy 2 | Hyperacusis | Charcot-Marie-Tooth Disease Type 4D | Demyelinating Diseases | Kindler Syndrome | Urea Cycle Disorder | Campomelic Dysplasia | Schindler Disease | Neonatal Progeroid Syndrome | COACH Syndrome | Intestinal Obstruction | Pulmonary Sclerosing Hemangioma | Colitis, Microscopic | Cryptorchidism | Basal Cell Nevus Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Hypertensive Nephropathy | Hypertension, Pulmonary | Splenomegaly | Agranulocytosis | Presbyopia | Cutaneous Lupus Erythematosus | Schizencephaly | Hepatic Steatosis | Dyslexia | Congenital Myasthenic Syndrome | Delirium | Pseudohypoparathyroidism Type 1C | Myositis | Encephalopathy, Ethylmalonic | Postpartum Depression | Spinocerebellar Ataxia Type 28 | Macular Corneal Dystrophy | Sezary Syndrome | Neurogenic Bladder | Episodic Ataxia | Ovarian Sex Cord-stromal Tumor | Endometritis | Neuroendocrine Cancer | Subcortical Band Heterotopia | Hepatitis E | Retinal Detachment | Congenital Heart Block | Hyperkalemic Periodic Paralysis | Glutaric Aciduria Type 2 | Hyperglycemia | X-linked Acrogigantism | Bernard-Soulier Syndrome | Anodontia | Prediabetes | Warsaw Breakage Syndrome | Cabezas Syndrome | Renpenning Syndrome | Facioscapulohumeral Muscular Dystrophy Type 1 | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Cannabis Abuse | Spinocerebellar Ataxia Type 31 | Prolidase Deficiency | Vitreoretinopathy, Proliferative | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Cystinuria | Sialidosis | McLeod Syndrome | Cluster Headache | Sleep Apnea, Obstructive | Muscular Dystrophy | Sialoadenitis | Absence Epilepsy | Systemic Mastocytosis | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Aicardi-Goutieres Syndrome | Kaposi Sarcoma | Myelofibrosis | Heimler Syndrome | Constipation | Cerebral Cavernous Malformations | Lyme Disease | Interstitial Lung Diseases | Myeloid Leukemia | Choroideremia | Blastoma, Pleuropulmonary | Molybdenum Cofactor Deficiency | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Bulimia Nervosa | Epidermolysis Bullosa Dystrophica | LEOPARD Syndrome | Lipoma | GATA2 Deficiency | MELAS Syndrome | Periodic Limb Movement Disorder | Metabolic Syndrome | Erythromelalgia | Angiosarcoma | Hypocalcemia