Disease

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

疾病靶点研报
Congenital Dyserythropoietic Anemia Type 4

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

Hyperammonemia | Lymphoma, AIDS-related | Cardiac Sarcoidosis | McLeod Syndrome | Spinocerebellar Ataxia Type 38 | Intracerebral Hemorrhage | Papilloma | 3-hydroxy-3-methylglutaric Aciduria | Oligospermia | Familial Hypertrophic Cardiomyopathy | Cryptococcal Meningitis | Rothmund-Thomson Syndrome | Spinocerebellar Ataxia Type 21 | Kawasaki Disease | Arrhythmogenic Right Ventricular Cardiomyopathy | Epidermolysis Bullosa Simplex | Hypopituitarism | Constipation | Granuloma Annulare | Reflex Epilepsy | Craniofacial Dysostosis | Fukuyama Congenital Muscular Dystrophy | Prune Belly Syndrome | Leishmaniasis, Cutaneous | Hereditary Sensory And Autonomic Neuropathy | Raine Syndrome | Microcephalic Primordial Dwarfism | Schizoaffective Disorder | Early Infantile Epileptic Encephalopathy 1 | VACTERL Association | Hypercholesterolemia | H Syndrome | Early Infantile Epileptic Encephalopathy 28 | Tyrosine Hydroxylase Deficiency | Dyslipidemia | Optic Nerve Diseases | Hyperuricemic Nephropathy, Familial Juvenile | Trichotillomania | Amebiasis | Personality Disorders | Tendinitis | Glycogen Storage Disease Type 0 | Mitochondrial Encephalomyopathy | Keratosis | Vitamin A Deficiency | Cold-induced Sweating Syndrome | Ophthalmoplegia | Barakat Syndrome | McKusick Type Metaphyseal Chondrodysplasia | Osteosclerosis | Ovarian Hyperstimulation Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Anorchia | Recurrent Respiratory Papillomatosis | Otosclerosis | Early Infantile Epileptic Encephalopathy 4 | Contact Dermatitis | Glycogen Storage Disease Type 6 | MIRAGE Syndrome | Hyperparathyroidism, Primary | Dental Caries | Gastritis | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Skin Carcinoma | Encephalopathy, Hepatic | Blepharitis | Hypertension, Portal | Metaphyseal Chondrodysplasia, Schmid Type | Malignant Fibrous Histiocytoma | Vertigo | Cholera | Acromegaly | Chronic Leukemia | Hoyeraal-Hreidarsson Syndrome | Histiocytic Sarcoma | GM2-gangliosidosis AB Variant | Prader-Willi Syndrome | Blue Nevus | Xeroderma Pigmentosum | Charcot-Marie-Tooth Disease Type 4B1 | Loeys-Dietz Syndrome | Chorioretinitis | Cardiomyopathy, Restrictive | Diabetes Insipidus, Nephrogenic | Spinocerebellar Ataxia Type 7 | Nephrotic Syndrome Type 1 | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Anti-glomerular Basement Membrane Disease | Pyelonephritis | Meesmann Corneal Dystrophy | GAPO Syndrome | Bardet-Biedl Syndrome | Retinitis Pigmentosa | Desmosterolosis | Aldosterone Deficiency | Schistosomiasis | Cancer, Breast | Incontinentia Pigmenti | Systemic Lupus Erythematosus | Vascular Calcification | Waardenburg Syndrome Type 1 | Acute Generalized Exanthematous Pustulosis | Myoclonic Atonic Epilepsy | Warsaw Breakage Syndrome | Acute Tubular Necrosis | Antley-Bixler Syndrome | Muscular Dystrophy | B-cell Prolymphocytic Leukemia | Tinea | Infectious Diarrhea | Muir-Torre Syndrome | Genitopatellar Syndrome | Precocious Puberty | Dermatitis Herpetiformis | Gray Platelet Syndrome | Niemann-Pick Disease | Stroke | Astrocytoma | Cervicitis | T-cell Chronic Lymphocytic Leukemia | Raynaud Phenomenon | Fuchs Heterochromic Iridocyclitis | Lipid Storage Myopathy | Cholelithiasis | Metatropic Dysplasia | Osteopetrosis | Fibromuscular Dysplasia | Spinal Muscular Atrophy | Vestibular Disease | Congenital Torticollis | Leishmaniasis, Visceral | Glycogen Storage Disease Type 1a | Adenomyosis | Stargardt Disease | Uveitis, Anterior | Congenital Dyserythropoietic Anemia Type 1 | Melanocytic Nevus | Charcot-Marie-Tooth Disease Type 4D | Chronic Enteropathy Associated With SLCO2A1 Gene | Papulopustular Rosacea | Hypoproteinemia, Hypercatabolic | Uremia | Thrombosis | Lesch-Nyhan Syndrome | Thyroid Dyshormonogenesis | Lassa Fever | Cenani-Lenz Syndactyly Syndrome | Hepatitis A | Wieacker-Wolff Syndrome | Hypotrichosis Simplex | Carbonic Anhydrase VA Deficiency | LMNA-related Congenital Muscular Dystrophy | Stevens-Johnson Syndrome | Intellectual Disability, Autosomal Dominant 5 | Dyggve-Melchior-Clausen Disease | Tylosis With Esophageal Cancer | Multiple Sclerosis | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Hyperinsulinism-hyperammonemia Syndrome | Glutaric Aciduria Type 3 | Eosinophilic Asthma | Temporal Lobe Epilepsy | Creatine Deficiency Syndrome | Chiari Malformation Type I | Dominant Optic Atrophy | Hereditary Sensory Neuropathy Type 1 | Neural Tube Defect | Uterine Leiomyoma | Lymphangioma | Eclampsia | Retinal Degeneration | Encephalocele | Rhabdoid Tumor | Phenylketonuria | Reticular Dysgenesis | Impulse Control Disorder | Osteomalacia | Iron Deficiency Anemia | Polyneuropathy | Encephalopathy | Retinitis Pigmentosa 3 | Multiple Epiphyseal Dysplasia | Arthritis, Reactive | Nemaline Myopathy | Cheilitis | Tic Disorder | Bulimia Nervosa | Coffin-Siris Syndrome | NDH Syndrome | Focal Dermal Hypoplasia | Neuroendocrine Cancer | Multiple Sclerosis, Secondary Progressive | Thalassemia | Ureteropelvic Junction Obstruction | Congenital Stromal Corneal Dystrophy | Leukoencephalopathy, Progressive Multifocal | CDKL5 Deficiency Disorder | Cancer, Skin | Multifocal Motor Neuropathy | Premature Ejaculation | Agnathia-Otocephaly Complex | Neurofibrosarcoma | Myelomeningocele | Goiter | Still Disease | Spinocerebellar Ataxia Type 20 | Intracranial Hypertension | Anal Fissure | Blastomycosis | Crohn's Disease | Plasma Cell Leukemia | Hypokalemic Periodic Paralysis | Pyruvate Kinase Deficiency | Parkinson Disease 6, Autosomal Recessive Early-onset | Hepatic Veno-occlusive Disease | Craniopharyngioma | Tularemia | Malignant Peripheral Nerve Sheath Tumor | Communication Disorders | X-linked Creatine Transporter Deficiency | Palmoplantar Keratoderma | Liver Failure | Marinesco-Sjogren Syndrome | Usher Syndrome Type IIC | Microcephaly, Seizures, And Developmental Delay | Cat Eye Syndrome | Spinocerebellar Ataxia Type 12 | Keratopathy | Pituitary Dwarfism | Compartment Syndrome | Autosomal Recessive Congenital Ichthyosis | Zollinger-Ellison Syndrome | Polycystic Liver | Thin Basement Membrane Disease | Venous Insufficiency | Williams Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Sarcoidosis | Phenylketonuria II | Glycogen Storage Disease | Mosaic Variegated Aneuploidy Syndrome 2 | Bursitis | Anorexia Nervosa | Apraxia | Aspergillosis | Sporadic Hemiplegic Migraine | Odonto-onycho-dermal Dysplasia | Keratoconjunctivitis | Corneal Dystrophy And Perceptive Deafness | Urea Cycle Disorder | Encephalitis, Tick-borne | Neuroblastoma | Pemphigus Foliaceus | Infantile Liver Failure Syndrome 1 | Ataxia-ocular Apraxia 2 | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Premenstrual Syndrome | Pneumonia, Bacterial | Lichen Planus | Bernard-Soulier Syndrome | Nicolaides-Baraitser Syndrome | Retinopathy, Diabetic | Sleep Apnea, Central | Fascioliasis | Retinal Dystrophy, Early-onset Severe | Esophagitis | Congenital Central Hypoventilation Syndrome | Dwarfism | Osteoporosis | Mucolipidosis | Exotropia | Noonan Syndrome-like Disorder With Loose Anagen Hair | Nephrocalcinosis | Agoraphobia | Unverricht-Lundborg Syndrome | Glycogen Storage Disease Type 4 | Hyperparathyroidism-jaw Tumor Syndrome | MELAS Syndrome | Hypogonadism | Ovarian Sex Cord-stromal Tumor | Hypervalinemia | Tyrosinemia Type 1 | Bronchiolitis | Greig Cephalopolysyndactyly Syndrome | Esophagitis, Eosinophilic | Panniculitis | Epidermodysplasia Verruciformis | Hereditary Folate Malabsorption | Trichuriasis | Cutaneous T-cell Lymphoma | Cancer, Colon | Short-chain Acyl-CoA Dehydrogenase Deficiency | Osteogenesis Imperfecta Type I | Aphasia | Angiosarcoma | Huntington's Disease | Von Willebrand Disease | Overactive Bladder | Osteogenesis Imperfecta Type VI | Steel Syndrome | Renal Failure | Costello Syndrome | Hereditary Hemorrhagic Telangiectasia Type 2 | Waardenburg Syndrome Type 2E | Chronic Granulomatous Disease, X-linked | Pseudohypoparathyroidism Type 1A | Urofacial Syndrome | Distal Myopathy 2 | Oculopharyngeal Muscular Dystrophy | Congenital Myopathy | Infertility | Congenital Stationary Night Blindness | Conjunctivitis | Anemia | Lyme Disease | Anovulation | Microphthalmia | Cryoglobulinemia | Chronic Idiopathic Myelofibrosis | Primary Hyperoxaluria | Bladder Exstrophy | Spinocerebellar Ataxia Type 27 | Behavioral Variant Of Frontotemporal Dementia | Congenital Sodium Diarrhea | Dubin-Johnson Syndrome | Hyperparathyroidism | Progressive Osseous Heteroplasia | Chromosome 9q34.3 Deletion Syndrome | Acrodermatitis | Hepatitis, Alcoholic | Heart Failure | Nevus | Tyrosinemia | Polycythemia Vera | Glomerulonephritis, Membranoproliferative | Lymphopenia | Nanophthalmos | Hyperthermia, Malignant | Angelman Syndrome | Walker-Warburg Syndrome | Non-Langerhans Cell Histiocytosis | Analgesia | Trimethylaminuria | Alazami Syndrome | Congenital Dysfibrinogenemia | Endocarditis | Spinocerebellar Ataxia Type 6 | Chromosome 5q Deletion Syndrome | Congenital Muscular Dystrophy | Emery-Dreifuss Muscular Dystrophy | REM Sleep Behavior Disorder | Hypogammaglobulinemia | Silver-Russell Syndrome | Nephronophthisis | Guillain-Barre Syndrome | High Molecular Weight Kininogen Deficiency | Li-Fraumeni Syndrome | Asplenia | Enterocolitis, Necrotizing | Blepharospasm | Lipodystrophy | Porphyria, Variegate | Intermittent Explosive Disorder | Roberts Syndrome | Asthma, Nocturnal | Neurofibromatosis Type 2 | Benign Hereditary Chorea | Carotid Artery Disease | Angiosarcoma Of The Breast | Strabismus | Metabolic Diseases | Narcolepsy | Otitis Externa | Chronic Lymphocytic Leukemia | Tyrosinemia Type 2 | Hereditary Coproporphyria | Chondrodysplasia Punctata 2, X-linked Dominant | Craniometaphyseal Dysplasia | Platelet Disorders | Thalassemia, Beta | Bronchitis, Chronic | Charcot-Marie-Tooth Disease, Type 2C | Autonomic Nervous System Disorders | Swine Influenza | Eccrine Porocarcinoma | Congenital Ichthyosiform Erythroderma | Familial Male-limited Precocious Puberty | Pyoderma Gangrenosum | CREST Syndrome | Polycystic Kidney, Autosomal Recessive | Molybdenum Cofactor Deficiency | Glaucoma, Congenital | Vici Syndrome | Rhinitis | Low Phospholipid Associated Cholelithiasis | Sialoadenitis | HIBCH Deficiency | Cramp Fasciculation Syndrome | Spinal Muscular Atrophy Type 2 | Tuberculosis