Tatton-Brown-Rahman Syndrome
Tatton-Brown-Rahman Syndrome
About the Disease
Tatton-Brown-Rahman Syndrome, also known as dnmt3a overgrowth syndrome, is related to overgrowth syndrome and adult syndrome. An important gene associated with Tatton-Brown-Rahman Syndrome is DNMT3A (DNA Methyltransferase 3 Alpha), and among its related pathways/superpathways are One-carbon metabolism and related pathways and Chromatin Regulation / Acetylation. The drugs Dasatinib and Teicoplanin have been mentioned in the context of this disorder. Affiliated tissues include myeloid, bone marrow and prostate, and related phenotypes are macrocephaly and proportionate tall stature
Common Targets
DNMT3A | H1-4

Note: If you'd like to get a target analysis report for Tatton-Brown-Rahman Syndrome, 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 Tatton-Brown-Rahman Syndrome at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.tech.
Other Diseases
Craniolenticulosutural Dysplasia | Supravalvular Aortic Stenosis | Lafora Disease | Hemophagocytic Lymphohistiocytosis | Coloboma | Porokeratosis | Schizencephaly | DNA Ligase IV Deficiency | 3-hydroxy-3-methylglutaric Aciduria | Hepatitis C, Chronic | Toxoplasmosis | Cholera | Pyoderma Gangrenosum | Hyperparathyroidism, Primary | Pigment Dispersion Syndrome | Alcoholism | Cancer, Skin | Micro Syndrome | Dystonia | Sleep Apnea, Central | Blepharospasm | Dysferlinopathy | Patent Foramen Ovale | Spinocerebellar Ataxia Type 12 | Osteogenesis Imperfecta Type II | Pierpont Syndrome | Spinocerebellar Ataxia Type 16 | Cavitary Optic Disc Anomalies | Fraser Syndrome | Urea Cycle Disorder | Anodontia | Riboflavin Transporter Deficiency Neuronopathy | Infertility, Male | Pleurisy | Martsolf Syndrome | Nemaline Myopathy | Craniofacial Dysostosis | Atherosclerosis | Charcot-Marie-Tooth Disease Axonal Type 2N | Otitis Media | Heart Septal Defects | Choroideremia | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Chordoid Glioma | Membranous Nephropathy | Bone Giant Cell Tumor | Headache | Postpoliomyelitis Syndrome | Platelet Disorders | Hyperlipidemia | Epilepsy, Generalized | Spinocerebellar Ataxia Type 7 | Papilloma | Tuberculosis | Tyrosinemia Type 1 | Spermatocele | Spinal And Bulbar Muscular Atrophy | Cancer, Bladder | Migraine | Geleophysic Dysplasia | Retinal Dystrophy, Early-onset Severe | Infantile Spasm | Cleidocranial Dysplasia | Tay-Sachs Disease | Allergic Contact Dermatitis | Metatropic Dysplasia | Thyroiditis, Autoimmune | Japanese Encephalitis | NGLY1 Deficiency | Spondylolisthesis | Mohr-Tranebjaerg Syndrome | Lymphoproliferative Disease, X-linked | Robinow Syndrome | C3 Glomerulopathy | Pachyonychia Congenita | Sickle Cell Anemia | Pulmonary Stenosis | FG Syndrome | Hydrolethalus Syndrome | Necrobiosis Lipoidica | Varicocele | Biotinidase Deficiency | X-linked Charcot-Marie-Tooth Disease | Pernicious Anemia | Triphalangeal Thumb-polysyndactyly Syndrome | Clouston Hidrotic Ectodermal Dysplasia | Glucagonoma | Aldosteronism | Sweet Syndrome | Cardiomyopathy, Hypertrophic | Ventricular Septal Defect | Synpolydactyly | Hyperthermia, Malignant | Anterior Segment Dysgenesis | Sandhoff Disease | Early Infantile Epileptic Encephalopathy 28 | Hyperlipidemia Type V | Familial Cerebral Amyloid Angiopathy | Panic Disorder | Hypotension, Orthostatic | Trigonocephaly | Hepatitis, Autoimmune | Cousin Syndrome | Hypertension | Focal Facial Dermal Dysplasia | Polycystic Kidney, Autosomal Dominant | Arthrogryposis | Ichthyosis Bullosa Of Siemens | Carey-Fineman-Ziter Syndrome | Osteitis | Exotropia | Oculocutaneous Albinism Type 1 | Rhabdoid Tumor | Psoriasis | Enlarged Vestibular Aqueduct | Retinitis Pigmentosa 3 | Anovulation | Pycnodysostosis | Seminoma | Pompe Disease | Keratocystic Odontogenic Tumor | Nephrosclerosis | Nutrition Disorders | Traboulsi Syndrome | Camptocormia | Hydrocephalus | Sponastrime Dysplasia | Waardenburg Syndrome Type 2 | Lamellar Ichthyosis | Donnai-Barrow Syndrome | Bulimia Nervosa | Microvillus Inclusion Disease | Swine Influenza | Anthrax | Lymphoma, AIDS-related | Hyperandrogenemia | Neurofibromatosis | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Epidermolysis Bullosa Dystrophica | Silicosis | Stomatitis | Hyperferritinemia-cataract Syndrome | Multiple Sclerosis, Secondary Progressive | Larsen Syndrome | Acute Generalized Exanthematous Pustulosis | Guanidinoacetate Methyltransferase Deficiency | Autoimmune Disease | Chylothorax, Congenital | Osteoporosis, Postmenopausal | Prolactinoma | Multisystemic Smooth Muscle Dysfunction Syndrome | Recurrent Respiratory Papillomatosis | Usher Syndrome | Optic Nerve Diseases | Asthma | Lennox-Gastaut Syndrome | Familial Hemiplegic Migraine | Non-bullous Congenital Ichthyosiform Erythroderma | Facioscapulohumeral Muscular Dystrophy Type 2 | Shock, Cardiogenic | Pulmonary Veno-occlusive Disease | Hyperbilirubinemia, Neonatal | Lymphoma | Danon Disease | Familial Episodic Pain Syndrome | Hereditary Elliptocytosis | Dubin-Johnson Syndrome | Cohen Syndrome | Partington Syndrome | Sturge-Weber Syndrome | Anti-NMDA Receptor Encephalitis | 3-methylglutaconic Aciduria Type IV | Pfeiffer Syndrome | Hereditary Xerocytosis | Lymphopenia | Temporal Lobe Epilepsy | Creutzfeldt-Jakob Disease | Sorsby Fundus Dystrophy | Reflex Epilepsy | Mitochondrial DNA Depletion Syndrome | Osteogenesis Imperfecta Type I | Familial Hyperaldosteronism | Glomerulonephritis, Membranoproliferative | Cutaneous Lupus Erythematosus | Epilepsy | Tularemia | Lymphoma, B-cell | Charcot-Marie-Tooth Disease, Type 2C | Waardenburg Syndrome Type 2A | Gerstmann-Straussler-Scheinker Syndrome | Achromatopsia | Acute Tubular Necrosis | Rett Syndrome | Lesch-Nyhan Syndrome | Twin-to-twin Transfusion Syndrome | Dowling-Degos Disease | Macular Corneal Dystrophy | Stromal Corneal Dystrophy | Hyperglycemia | Retinopathy Of Prematurity | Hepatitis, Chronic | Fahr Disease | Leukoencephalopathy, Progressive Multifocal | Chronic Granulomatous Disease, X-linked | Angelman Syndrome | CEDNIK Syndrome | Conn Syndrome | Gastroschisis | Delayed Sleep Phase Syndrome | Vitreoretinal Degeneration, Snowflake Type | Osteoglophonic Dysplasia | Mosaic Variegated Aneuploidy Syndrome 2 | Tatton-Brown-Rahman Syndrome | Lichen Sclerosus | Metanephric Adenoma | Cystitis | Neurocutaneous Melanocytosis | Spinocerebellar Ataxia Type 3 | Lymphoproliferative Disorders | Pure Autonomic Failure | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Giant Cell Glioblastoma | Parkinson Disease 6, Autosomal Recessive Early-onset | Relapsing Polychondritis | Spondylometaphyseal Dysplasia | Antenatal Bartter Syndrome Type 1 | Chudley-McCullough Syndrome | Palsy, Cerebral | Glycogen Storage Disease | Loeys-Dietz Syndrome Type 4 | Hypereosinophilic Syndrome | Niemann-Pick Disease, Type C | Retinal Vasculitis | Tyrosine Hydroxylase Deficiency | Corneal Edema | Hepatic Veno-occlusive Disease | Cherubism | Erysipelas | Vogt-Koyanagi-Harada Syndrome | Gyrate Atrophy Of The Choroid And Retina | Amebiasis | Tyrosinemia Type 2 | Pierson Syndrome | Encephalopathy, Glycine | Juvenile Xanthogranuloma | Brachydactyly | Anencephaly | Vascular Calcification | Hemolytic Anemia | Familial Partial Lipodystrophy | Atopic Dermatitis | Borderline Personality Disorder | Protein S Deficiency | Multicentric Carpotarsal Osteolysis Syndrome | Myelitis | Exfoliative Dermatitis | Meniere's Disease | Left Ventricular Noncompaction | Wilson's Disease | Subacute Sclerosing Panencephalitis | Rash | Diffuse Intrinsic Pontine Glioma | Transcobalamin Deficiency | Norrie Disease | Tricho-hepato-enteric Syndrome | Hypertension, Portal | Gastric Atrophy | Colorectal Adenoma | Tibial Muscular Dystrophy | Cholestasis, Intrahepatic | Cold-induced Sweating Syndrome | Juvenile Myoclonic Epilepsy | Kernicterus | HANAC Syndrome | Genee-Wiedemann Syndrome | Leukoplakia | Sarcosinemia | McKusick Type Metaphyseal Chondrodysplasia | Marfan Syndrome | Nicotine Dependence | Pontocerebellar Hypoplasia Type 2 | Omenn Syndrome | Hereditary Inclusion Body Myopathy | Urofacial Syndrome | Hypophosphatasia | Primary Familial Brain Calcification | Bardet-Biedl Syndrome | Polymicrogyria | Ileitis | Smith-Magenis Syndrome | Bone Marrow Necrosis | Schizophrenia, Paranoid | Cirrhosis | Proteasome-associated Autoinflammatory Syndrome 2 | Bronchiolitis | Irritable Bowel Syndrome | Pathological Gambling | Autosomal Recessive Spastic Paraplegia Type 75 | Amenorrhea | MIRAGE Syndrome | Brugada Syndrome 1 | Molybdenum Cofactor Deficiency | Meningeal Melanocytoma | Prune Belly Syndrome | Arteriosclerosis | Chorioretinitis | Pituitary Disorders | Glioma | Scapuloperoneal Spinal Muscular Atrophy | Williams Syndrome | Aspartylglycosaminuria | Benign Hereditary Chorea | Mitochondrial DNA Depletion Syndrome 13 | Meningococcal Infections | Coenzyme Q10 Deficiency | Raynaud Phenomenon | Blomstrand Osteochondrodysplasia | Histiocytosis | Hyperinsulinism-hyperammonemia Syndrome | Fanconi Anemia | Lupus Erythematosus | Beckwith-Wiedemann Syndrome | Tetraplegia | Spitz Nevus | Carbonic Anhydrase VA Deficiency | Acquired Partial Lipodystrophy | Ichthyosis Hystrix, Curth-Macklin Type | Antisocial Personality Disorder | Stargardt Disease | Hypolipoproteinemia | Scleritis | Cannabis Abuse | Weill-Marchesani Syndrome | Carcinoma, Signet Ring Cell | Congenital Disorders Of Glycosylation Type II | Charcot-Marie-Tooth Disease Type 2D | ADNP Syndrome | Connective Tissue Disorders | Mast Cell Leukemia | Progressive Osseous Heteroplasia | Chondroma | Hereditary Multiple Exostoses | Neurofibrosarcoma | Lymphangiomatosis | Neurofibromatosis Type 1 | Porphyria Cutanea Tarda | Muir-Torre Syndrome | Diffuse Palmoplantar Keratoderma | Blepharoconjunctivitis | Hypercalciuria | Nicotine Addiction | Cyclic Vomiting Syndrome | Carcinoma, Transitional Cell | Carcinoma In Situ | Acute Kidney Injury | Persistent Mullerian Duct Syndrome | Cardiomyopathy, Peripartum | Cheilitis | Van Der Knaap Disease | Familial Retinal Arterial Macroaneurysm | Sarcoma, Ewing | Best Macular Dystrophy | Pulmonary Alveolar Proteinosis | Epidermolysis Bullosa Simplex, Localized | Glycogen Storage Disease Type 6 | Myasthenia Gravis | Encephalopathy, Ethylmalonic | Spina Bifida | Scabies | Spinocerebellar Ataxia Type 13 | Tendinitis | Adenylosuccinate Lyase Deficiency | Congenital Muscular Dystrophy | Juvenile Polyposis | Silver-Russell Syndrome | Phenylketonuria II | Fundus Albipunctatus | Glycogen Storage Disease Type 1b | Arthropathy | Mycosis Fungoides | Primary Torsion Dystonia | Whipple's Disease | Rubeosis Iridis | Sezary Syndrome | POEMS Syndrome | Infertility | Meleda Disease | Osteopetrosis | Bronchitis | Narcolepsy | Renal Hypouricemia | Osteoarthritis | Aarskog-Scott Syndrome | Familial Exudative Vitreoretinopathy | Craniometaphyseal Dysplasia | Distal Myopathy | Intellectual Disability, Autosomal Dominant 5 | Osteogenesis Imperfecta | Ligneous Conjunctivitis | Yellow Fever