Duodenal Atresia

About the Disease
Duodenal Atresia, also known as duodenal stenosis, is related to feingold syndrome 1 and pancreas, annular. An important gene associated with Duodenal Atresia is GUCY2C (Guanylate Cyclase 2C), and among its related pathways/superpathways are Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers and Pluripotent stem cell differentiation pathway. Affiliated tissues include small intestine, pancreas and heart, and related phenotypes are polyhydramnios and duodenal atresia

Common Targets
ITGA2 | SERPINE1 | NPPA | ADRB2 | RFX6

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

Other Diseases

Cockayne Syndrome | COACH Syndrome | Osteosarcoma | Hereditary Neuropathy With Liability To Pressure Palsies | Gestational Trophoblastic Disease | Hypopigmentation | Carcinoid Tumor | T-cell Leukemia | Angiosarcoma Of The Breast | Persistent Truncus Arteriosus | Paternal Uniparental Disomy Of Chromosome 14 | Hermansky-Pudlak Syndrome | Esophageal Adenocarcinoma | Vertigo | Spinocerebellar Ataxia Type 40 | VACTERL/VATER Association | Asperger Syndrome | Dermatomyositis | Dystrophy, Cone-rod | Atrial Septal Defect | Cerebral Amyloid Angiopathy | Basal Ganglia Cerebrovascular Disease | Malnutrition | Spinocerebellar Ataxia Type 17 | Sclerosing Cholangitis | Multiple Sclerosis, Chronic Progressive | KBG Syndrome | Gallstones | Genee-Wiedemann Syndrome | Long QT Syndrome Type 2 | Distal Myopathy 2 | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Presbycusis | Orotic Aciduria | Adenylosuccinate Lyase Deficiency | Thyroiditis, Autoimmune | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Retinal Detachment | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Lennox-Gastaut Syndrome | Teratozoospermia | Chronic Granulomatous Disease | Bicuspid Aortic Valve | Metabolic Syndrome | Gastroschisis | Galactosialidosis | Desmosterolosis | Ameloblastoma | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Gliosarcoma | Bone Marrow Necrosis | Aspartylglycosaminuria | Sarcosinemia | Familial Isolated Hyperparathyroidism | Optic Neuropathy | Macular Corneal Dystrophy Type 1 | Blood Protein Disorders | Cerebellofaciodental Syndrome | Craniofrontonasal Syndrome | Lymphangiomatosis | Choroideremia | Takenouchi-Kosaki Syndrome | Torticollis | Low Tension Glaucoma | Hepatic Steatosis | Primary Aldosteronism | Peeling Skin Syndrome, Acral Type | Bethlem Myopathy | Haim-Munk Syndrome | Muir-Torre Syndrome | Leiomyosarcoma | Infantile Refsum Disease | Angina Pectoris | Epidermolysis Bullosa Simplex, Localized | Chronic Beryllium Disease | Genitopatellar Syndrome | Becker Muscular Dystrophy | Trimethylaminuria | Spondylocarpotarsal Synostosis Syndrome | Histiocytic Sarcoma | Light Chain Amyloidosis | Antithrombin III Deficiency | Wolfram Syndrome | Myofibrillar Myopathy | Liver Failure, Acute Infantile | Leber Hereditary Optic Neuropathy | Chronic Enteropathy Associated With SLCO2A1 Gene | Nephrotic Syndrome | Antisynthetase Syndrome | Papilloma | Spondylocostal Dysostosis | Lymphedema | Multiple Sclerosis, Secondary Progressive | Triple A Syndrome | Multiple Sclerosis | Diabetes Insipidus, Neurogenic | Glanzmann Thrombasthenia | Primary Familial Brain Calcification | Stevens-Johnson Syndrome | Infectious Diarrhea | Nanophthalmos | Acute Tubular Necrosis | Hidradenitis | Glutathione Synthetase Deficiency | Atelosteogenesis Type 1 | Unverricht-Lundborg Syndrome | Spinocerebellar Ataxia Type 28 | Filariasis | Anthrax | Multiple Sulfatase Deficiency | Palmoplantar Keratoderma | Heart Block | Primary Progressive Aphasia | Rotor Syndrome | X-linked Creatine Transporter Deficiency | Barrett Esophagus | Arthrogryposis | Subcortical Band Heterotopia | Graves Disease | Idiopathic Pulmonary Fibrosis | Hypertension, Renovascular | Gilbert Syndrome | Twin-to-twin Transfusion Syndrome | GATA2 Deficiency | Aplastic Anemia | Snyder-Robinson Syndrome | Ellis-Van Creveld Syndrome | Ehlers-Danlos Syndrome | Nemaline Myopathy | Aneurysm, Abdominal Aortic | Nager Acrofacial Dysostosis | Situs Inversus | Cramp Fasciculation Syndrome | Trichomegaly | Atherosclerosis | Absence Epilepsy | Dengue Shock Syndrome | Spinal Muscular Atrophy Type 3 | Familial Exudative Vitreoretinopathy | Auriculocondylar Syndrome | Lactose Intolerance | Multicystic Renal Dysplasia | Geleophysic Dysplasia | Carbohydrate Metabolism Disorders | Nicotine Addiction | Angiomyolipoma | Retinoschisis | Gingivitis | Partington Syndrome | Scleroderma, Diffuse | Keratopathy | Gynecomastia | Plasmacytoma | Cocaine-Related Disorders | Retinopathy Of Prematurity | Pupil Disorders | Optic Atrophy 2 | Corticobasal Syndrome | Sleep Apnea, Obstructive | Nephronophthisis | X-linked Charcot-Marie-Tooth Disease | Cold Agglutinin Disease | Glucagonoma | Spinocerebellar Ataxia Type 2 | Axenfeld-Rieger Syndrome | Carcinoid Syndrome | Familial Partial Lipodystrophy | Incontinentia Pigmenti | Behavioral Variant Of Frontotemporal Dementia | Metachromatic Leukodystrophy | Proteus Syndrome | Nicotine Dependence | Hypogammaglobulinemia | Waardenburg Syndrome Type 4A | Cyclic Vomiting Syndrome | Pituitary Disorders | Dysfibrinogenemia | Amelanotic Melanoma | Pneumonia, Bacterial | Adult Polyglucosan Body Disease | Glaucoma, Congenital | Gastritis, Atrophic | Retinitis Pigmentosa 3 | Tricho-hepato-enteric Syndrome | Sarcomatoid Carcinoma Of The Lung | Cholelithiasis | Left Ventricular Noncompaction | Nasodigitoacoustic Syndrome | Lymphoma, Follicular | Nevus | Anorectal Fistula | Hodgkin Lymphoma | Herpes Genitalis | Coenzyme Q10 Deficiency | Alopecia Totalis | Neurodevelopmental Disorders | Loeys-Dietz Syndrome Type 4 | Dermatofibrosarcoma | Iron Overload | Obsessive-compulsive Disorder | Hyperbilirubinemia, Neonatal | Benign Familial Pemphigus | Combined Pituitary Hormone Deficiency | Spinal Cord Diseases | Juvenile Polyposis | Holoprosencephaly | Thyroid Hormone Resistance | Ischemia | Cholera | Colitis, Lymphocytic | Antiphospholipid Syndrome | Hypersensitivity | Hemorrhoids | Maternally Inherited Diabetes And Deafness | Eccrine Porocarcinoma | Noonan Syndrome | Cutaneous Mastocytosis | Netherton Syndrome | Warsaw Breakage Syndrome | VEXAS Syndrome | Xeroderma Pigmentosum Variant Type | Hyperammonemia | Milk Allergy | Johanson-Blizzard Syndrome | Aldosterone Synthase Deficiency | Varices | Acute Motor Axonal Neuropathy | Cancer, Bladder | Diabetes Insipidus | Calcium Pyrophosphate Deposition Disease | 3-methylglutaconic Aciduria Type I | Epidermolysis Bullosa Dystrophica | Scabies | Giant Cell Glioblastoma | Nicolaides-Baraitser Syndrome | Congenital Diaphragmatic Hernia | NDH Syndrome | Glomerulonephritis | Large Granular Lymphocytic Leukemia | Borjeson-Forssman-Lehmann Syndrome | Endophthalmitis | Relapsing Polychondritis | L-2-Hydroxyglutaric Aciduria | Varicocele | Steel Syndrome | Pituitary Stalk Interruption Syndrome | Bulimia Nervosa | Iron Metabolism Disorders | Cousin Syndrome | Familial Hyperaldosteronism | Congenital Afibrinogenemia | Cutaneous Lupus Erythematosus | Myoclonus-dystonia Syndrome | Hemolytic Uremic Syndrome, Atypical | Addison Disease | Blomstrand Osteochondrodysplasia | Hypobetalipoproteinemias | Kaposi Sarcoma | Smith-Magenis Syndrome | Spinocerebellar Ataxia Type 10 | Malaria, Cerebral | Fontaine Progeroid Syndrome | DNA Ligase IV Deficiency | Hypertension | Hemochromatosis | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Hartnup Disease | Primary Hyperoxaluria Type 1 | Carey-Fineman-Ziter Syndrome | Carbonic Anhydrase VA Deficiency | Hyperkeratosis | Dyskeratosis Congenita | Multifocal Motor Neuropathy | Chromosome 16p11.2 Deletion Syndrome | Hemochromatosis Type 1 | Galactosemia | Familial Glucocorticoid Deficiency | Meesmann Corneal Dystrophy | Whipple's Disease | Pfeiffer Syndrome | Discoid Lupus Erythematosus | Benign Familial Neonatal Convulsions | Vasculitis | Sweet Syndrome | Congenital Disorders Of Glycosylation | Astigmatism | Sleep Apnea | CREST Syndrome | Congenital Bile Acid Synthesis Defect | Diffuse Mesangial Sclerosis | Oculodentodigital Dysplasia | Leishmaniasis, Cutaneous | Tonsillitis | Familial Cerebral Amyloid Angiopathy | Amyotrophic Lateral Sclerosis | Pneumoconiosis | Strabismus | Sarcoidosis | Primary Carnitine Deficiency | PASLI Disease | Osteoporosis, Postmenopausal | Synovitis | Mixed Connective Tissue Disease | Tyrosine Hydroxylase Deficiency | Congenital Hereditary Endothelial Dystrophy Type II | Primary Torsion Dystonia | Celiac Disease | Congenital Hemolytic Anemia | Congenital Heart Block | Acute Leukemia | Blastoma, Pleuropulmonary | Pleural Tuberculosis | Carbamoyl Phosphate Synthetase I Deficiency | Glycogen Storage Disease Type 3 | Heroin Dependence | Asplenia | Cranioectodermal Dysplasia | Schuurs-Hoeijmakers Syndrome | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Cancer, Prostate | Harlequin Ichthyosis | Acromicric Dysplasia | Smith-Lemli-Opitz Syndrome | Bipolar Disorder | Hypophosphatasia | Holt-Oram Syndrome | Neuronal Ceroid Lipofuscinosis | Pontocerebellar Hypoplasia Type 7 | Persistent Hyperplastic Primary Vitreous | Niemann-Pick Disease, Type B | Neurofibroma | Acrodermatitis | Glycogen Storage Disease Type 1a | Infantile Neuroaxonal Dystrophy | Nail-Patella Syndrome | Nemaline Myopathy 10 | Adams-Oliver Syndrome | Encephalopathy, Glycine | Cheilitis | Cysticercosis | Hypertensive Nephropathy | Citrullinemia | Rolandic Epilepsy | Chronic Mucocutaneous Candidiasis | Cerebellar Ataxia, Cayman Type | Hereditary Pyropoikilocytosis | Kidney Stones | Carney-Stratakis Syndrome | Wiskott-Aldrich Syndrome | Thrombosis | Oculopharyngeal Muscular Dystrophy | Ventricular Septal Defect | Basal Cell Nevus Syndrome | Chediak-Higashi Syndrome | Chitayat Syndrome | Arthritis, Psoriatic | Lichen Sclerosus | Glutaric Aciduria Type 3 | Panniculitis | Hyperinsulinism-hyperammonemia Syndrome | Hyperhomocysteinemia | Inflammatory Bowel Disease | Creatine Deficiency Syndrome Due To AGAT Deficiency | Ghosal Syndrome | Chronic Neutrophilic Leukemia | 3-methylcrotonyl-CoA Carboxylase Deficiency | Paroxysmal Kinesigenic Dyskinesia | Hereditary Sensory And Autonomic Neuropathy | Obesity | Polymyositis | Fukuyama Congenital Muscular Dystrophy | Necrotizing Autoimmune Myopathy | Spinal And Bulbar Muscular Atrophy | Polycystic Kidney, Autosomal Recessive | Localized Scleroderma | CHARGE Syndrome | Neuromyelitis Optica | Hepatoblastoma | Hyperlipidemia | Spinal Muscular Atrophy | Spinocerebellar Ataxia Type 23 | Mucormycosis | Dyslexia | Language Disorders | Priapism | Cardiospondylocarpofacial Syndrome | Sialoadenitis | Heimler Syndrome | Cushing Syndrome | Cancer, Colon | Ocular Hypertension | Polyradiculopathy | Weill-Marchesani Syndrome | Retinitis | Ornithine Transcarbamylase Deficiency | Epiphyseal Chondrodysplasia, Miura Type | Shock, Cardiogenic | Liver Diseases | Peroxisomal Disorder | Vici Syndrome