Disease

Branchiootorenal Syndrome

About the Disease
Branchiootorenal Syndrome, also known as branchio-oto-renal syndrome, is related to branchiootorenal syndrome 1 and branchiootic syndrome 1. An important gene associated with Branchiootorenal Syndrome is EYA1 (EYA Transcriptional Coactivator And Phosphatase 1), and among its related pathways/superpathways are Genes controlling nephrogenesis and Development of ureteric collection system. Affiliated tissues include tonsil, kidney and bone, and related phenotypes are hearing impairment and external ear malformation

Common Targets
SALL1 | EYA1 | SIX5 | SIX1

疾病靶点研报
Branchiootorenal Syndrome

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

Other Diseases

Disseminated Intravascular Coagulation | Diffuse Mesangial Sclerosis | Aphasia | Patent Ductus Arteriosus | Pemphigus | Conjunctivitis | Microcephalic Primordial Dwarfism | Facioscapulohumeral Muscular Dystrophy | Thyrotoxic Periodic Paralysis | Dystonia | Familial Isolated Hyperparathyroidism | Beare-Stevenson Syndrome | Peyronie's Disease | Thyroid Hormone Resistance | Astrocytoma, Anaplastic | Cerebrotendinous Xanthomatosis | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Colitis, Collagenous | Glycogen Storage Disease Type 1a | Nephroblastoma | Otitis Media | Cardiofaciocutaneous Syndrome | Tuberculous Meningitis | Spina Bifida | Lipid Storage Diseases | Trismus-pseudocamptodactyly Syndrome | Loeys-Dietz Syndrome Type 4 | Withdrawal Syndrome | Keratoconjunctivitis | Asthma, Nocturnal | Persistent Truncus Arteriosus | Coenzyme Q10 Deficiency | Lymphoma, AIDS-related | Pancytopenia | Primary Carnitine Deficiency | Optic Atrophy 2 | Protein S Deficiency | Hypotonia-cystinuria Syndrome | Thyroid Dyshormonogenesis | Cataract | Adenoid Cystic Carcinoma | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Retinal Diseases | Cryptosporidiosis | Scleroderma | 3-M Syndrome | Blue Rubber Bleb Nevus Syndrome | Carbonic Anhydrase VA Deficiency | Macular Degeneration | Cholera | Mucormycosis | Osteopathia Striata With Cranial Sclerosis | Renal Hypouricemia | Familial Dysautonomia | X-linked Acrogigantism | Raine Syndrome | Heart Block | Open-angle Glaucoma | Nail Disorder, Nonsyndromic Congenital | Coffin-Lowry Syndrome | Acquired Partial Lipodystrophy | Osteoporosis | Fukuyama Congenital Muscular Dystrophy | Incontinentia Pigmenti | Muir-Torre Syndrome | Chronic Granulomatous Disease, X-linked | Borderline Personality Disorder | Johanson-Blizzard Syndrome | Japanese Encephalitis | Dengue Hemorrhagic Fever | Primary Pigmented Nodular Adrenocortical Disease | Carotid Artery Disease | Spitzoid Melanoma | Chorea | Diastrophic Dysplasia | Allan-Herndon-Dudley Syndrome | Paget's Disease Of The Breast | Intermittent Claudication | Postpoliomyelitis Syndrome | Cysticercosis | Cholesteryl Ester Storage Disease | Carcinoma In Situ | Wiskott-Aldrich Syndrome | Nephrotic Syndrome Type 1 | Familial Partial Lipodystrophy | Larsen Syndrome | Heart Septal Defects | Bardet-Biedl Syndrome | Citrullinemia | Platelet Disorders | Vitreoretinal Degeneration, Snowflake Type | Congenital Disorders Of Glycosylation Type II | Mesothelioma, Malignant | Amyotrophic Lateral Sclerosis, Juvenile | Frontotemporal Dementia | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Adenoma, Pleomorphic | Infertility | GLUT1 Deficiency Syndrome | Mitochondrial DNA Depletion Syndrome 13 | Cryptorchidism | Familial Thoracic Aortic Aneurysm | Charcot-Marie-Tooth Disease, Type 2C | VEXAS Syndrome | Spinocerebellar Ataxia Type 5 | Thromboembolism | Cleidocranial Dysplasia | Werner's Syndrome | Gallstones | Osteogenesis Imperfecta Type II | Hepatitis A | Chondrodysplasia Punctata | Speech Disorders | Neural Tube Defect | Unverricht-Lundborg Syndrome | Compartment Syndrome | Esophagitis | Traboulsi Syndrome | Keratosis | Peeling Skin Syndrome Type B | Generalized Epilepsy With Febrile Seizures Plus | Fibrosarcoma | Congenital Absence Of Vas Deferens | Eclampsia | Medulloblastoma | Anthrax | Aneurysm, Thoracic Aortic | Lung Diseases | Frontometaphyseal Dysplasia | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hyperinsulinemic Hypoglycemia | Fontaine Progeroid Syndrome | Pycnodysostosis | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Polycystic Ovary Syndrome | Lymphangioleiomyomatosis | Neurogenic Bladder | Deafness, Dystonia, And Cerebral Hypomyelination | Primary Familial Brain Calcification | Hereditary Sensory And Autonomic Neuropathy | Fibrosis | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Alcoholism | Goldenhar Syndrome | Hydronephrosis | Intracranial Hypertension | Schwartz-Jampel-Aberfeld Syndrome | Cholestasis | Torticollis | Hypolipoproteinemia | Waardenburg Syndrome Type 2 | Basal Cell Nevus Syndrome | Birt-Hogg-Dube Syndrome | Becker Muscular Dystrophy | Pontocerebellar Hypoplasia | Chromosome 9q34.3 Deletion Syndrome | Thyroiditis | Behcet's Disease | VACTERL/VATER Association | Lesch-Nyhan Syndrome | Ichthyosis, X-linked | Colorectal Adenoma | Meniere's Disease | Syphilis | Cutaneous Lupus Erythematosus | Hyperinsulinism-hyperammonemia Syndrome | Angiosarcoma | Rickets | Atrioventricular Septal Defect | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Pontocerebellar Hypoplasia Type 7 | Charcot-Marie-Tooth Disease, Type 2 | Early Infantile Epileptic Encephalopathy 1 | Eating Disorder | Hemophagocytic Lymphohistiocytosis | Exostoses | Auriculocondylar Syndrome | Cryoglobulinemia | Stroke, Hemorrhagic | Actinomycetoma | Genee-Wiedemann Syndrome | Narcolepsy | Early Infantile Epileptic Encephalopathy 4 | Rubeosis Iridis | Mandibuloacral Dysplasia With Type A Lipodystrophy | Oligoasthenoteratozoospermia | Congenital Sodium Diarrhea | Hyperekplexia | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Polycythemia Vera | Tracheal Disorders | Craniosynostosis | Scapuloperoneal Spinal Muscular Atrophy | Myhre Syndrome | Behavioral Variant Of Frontotemporal Dementia | Hyperprolactinemia | Lipodystrophy | Osteogenesis Imperfecta Type III | Dysferlinopathy | Rotor Syndrome | Retinal Coloboma | Malignant Fibrous Histiocytoma | Pseudoachondroplasia | Spinocerebellar Ataxia Type 8 | Goiter, Nodular | Usher Syndrome | Fibromuscular Dysplasia | Cramp Fasciculation Syndrome | Mountain Sickness | Spitz Nevus | Uterine Leiomyoma | Leiomyosarcoma | Uremia | Spinocerebellar Ataxia Type 38 | Fanconi Anemia | Leukocyte Adhesion Deficiency | Low Tension Glaucoma | Vitiligo | Common Cold | Esophageal Motility Disorders | Obesity | Erythematotelangiectatic Rosacea | Adenosine Deaminase 2 Deficiency | Early Infantile Epileptic Encephalopathy 28 | Prolactinoma | Meningeal Melanocytoma | Small Lymphocytic Lymphoma | Triphalangeal Thumb-polysyndactyly Syndrome | Seasonal Mood Disorder | Teratozoospermia | Neovascular Glaucoma | Sick Sinus Syndrome | L-2-Hydroxyglutaric Aciduria | Aicardi-Goutieres Syndrome | POEMS Syndrome | DICER1 Syndrome | Stomatitis | Neurofibromatosis-Noonan Syndrome | Exocrine Pancreatic Insufficiency | Dent Disease | Iron Deficiency Anemia | Adenosine Deaminase Deficiency | Crimean-Congo Hemorrhagic Fever | Primrose Syndrome | Interstitial Lung Diseases | Pleural Tuberculosis | Donnai-Barrow Syndrome | Adult Polyglucosan Body Disease | Acrodermatitis Enteropathica | Pendred Syndrome | Infertility, Male | Blepharospasm | Adenomatoid Tumor | Choroideremia | Corneal Dystrophy | Pierre Robin Syndrome | Hypocalcemia | Erythropoietic Protoporphyria | Autism Spectrum Disorders | Pheochromocytoma | Persistent Hyperplastic Primary Vitreous | Endophthalmitis | Renpenning Syndrome | Aplasia Cutis Congenita | Proteasome-associated Autoinflammatory Syndrome 2 | Wilson's Disease | Atrial Septal Defect | Greig Cephalopolysyndactyly Syndrome | Malaria, Cerebral | Microcephaly | Porphyria | Autosomal Recessive Spastic Paraplegia Type 54 | Transcobalamin Deficiency | Perivascular Epithelioid Cell Tumor | Chromosome 8q21.11 Deletion Syndrome | Hypoproteinemia, Hypercatabolic | Currarino Syndrome | Pneumonia, Mycoplasma | Corneal Neovascularization | Alzheimer Disease, Late Onset | Placenta Previa | Sarcosinemia | Benign Familial Infantile Seizures | B-cell Chronic Lymphocytic Leukemia | Hereditary Pyropoikilocytosis | Hemorrhagic Disorders | Pseudohypoparathyroidism Type 2 | Warsaw Breakage Syndrome | Babesiosis | Sotos Syndrome | Blepharoconjunctivitis | Chronic Neutrophilic Leukemia | Hemochromatosis Type 1 | Keratopathy | Lymphoproliferative Disorders | Chylomicron Retention Disease | Hyperandrogenemia | Retinal Vasculitis | Porphyria, Variegate | Dental Caries | Vitamin K Deficiency | Amyloidosis | Pupil Disorders | Cerebellofaciodental Syndrome | Urethritis | Veno-occlusive Disease | Heavy Chain Disease | Snyder-Robinson Syndrome | Split Hand-foot Malformation | Cole-Carpenter Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Early Infantile Epileptic Encephalopathy 13 | Budd-Chiari Syndrome | Hypercholesterolemia, Familial | Microphthalmia, Syndromic 7 | Cervical Dystonia | Central Retinal Artery Occlusion | Bronchiectasis | Juvenile Xanthogranuloma | Brugada Syndrome 1 | Rheumatic Heart Disease | Renal Oncocytoma | Ophthalmia, Sympathetic | Phosphoglycerate Dehydrogenase Deficiency | Chylothorax, Congenital | Sclerocornea | Mood Disorder | Parapsoriasis | 3-methylglutaconic Aciduria Type I | Asphyxia Neonatorum | Bursitis | Hydrolethalus Syndrome | Blomstrand Osteochondrodysplasia | Erdheim-Chester Disease | Atelosteogenesis Type 1 | Gigantism | Spinocerebellar Ataxia | Fabry's Disease | Charcot-Marie-Tooth Disease Type 2E | Pulmonary Sclerosing Hemangioma | Pseudohypoaldosteronism | H Syndrome | Pulmonary Vein Stenosis | Discoid Lupus Erythematosus | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Paraganglioma | Polycythemia | Diffuse Palmoplantar Keratoderma | Osteogenesis Imperfecta Type IV | Hypodontia | Hydrocephalus, Normal Pressure | Hemochromatosis | Fucosidosis | Anemia | Costello Syndrome | Oculocutaneous Albinism | Pseudomyxoma Peritonei | Eosinophilic Asthma | Osteoglophonic Dysplasia | Cranial Nerve Disease | Familial Advanced Sleep Phase Syndrome | Tardive Dyskinesia | Castleman Disease | Headache | X-linked Creatine Transporter Deficiency | Plasma Cell Dyscrasia | Blastoma, Pleuropulmonary | Papillon-Lefevre Syndrome | Spondyloperipheral Dysplasia | Anovulation | Stevens-Johnson Syndrome | Craniometaphyseal Dysplasia | Premature Ejaculation | Hyperkalemic Periodic Paralysis | Corneal Dystrophy And Perceptive Deafness | 3C Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Systemic Lupus Erythematosus | Long QT Syndrome Type 3 | Sarcoidosis, Pulmonary | Bicuspid Aortic Valve | Intracerebral Hemorrhage | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Osteogenesis Imperfecta Type I | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | CHARGE Syndrome | Fahr Disease | Hyper IgE Syndrome | Nephrocalcinosis | Nicotine Addiction | Meningococcal Infections | Epidermolysis Bullosa Simplex, Localized | Sleep Apnea, Central | Ebstein Anomaly | Fibronectin Glomerulopathy | DOCK8 Immunodeficiency Syndrome | Hyperhomocysteinemia | Sponastrime Dysplasia | Inflammatory Bowel Disease | Transthyretin-related Amyloidosis