Disease

Intestinal Obstruction

About the Disease
Intestinal Obstruction, also known as inspissated milk syndrome, is related to hirschsprung disease 1 and ileus, and has symptoms including abdominal pain, constipation and diarrhea. An important gene associated with Intestinal Obstruction is SLC26A3 (Solute Carrier Family 26 Member 3), and among its related pathways/superpathways are Signal Transduction and Cytoskeletal Signaling. The drugs Benzocaine and Tannic acid have been mentioned in the context of this disorder. Affiliated tissues include kidney, small intestine and colon, and related phenotypes are no effect and no effect

Common Targets
FLNA

疾病靶点研报
Intestinal Obstruction

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

Other Diseases

6-pyruvoyl-tetrahydropterin Synthase Deficiency | Osteoglophonic Dysplasia | Ganglioglioma | Nager Acrofacial Dysostosis | Histiocytic Sarcoma | Juvenile Myoclonic Epilepsy | Encephalopathy, Ethylmalonic | Apert Syndrome | Hemoglobinopathies | Parkinsonism | Hydronephrosis | Sensory Neuropathy | POEMS Syndrome | Tylosis With Esophageal Cancer | Early Infantile Epileptic Encephalopathy 1 | Alopecia Totalis | Obesity | Angiomyolipoma | Juvenile Xanthogranuloma | Tay-Sachs Disease | Stomatitis | Neurofibroma, Plexiform | Multicentric Carpotarsal Osteolysis Syndrome | Progressive Osseous Heteroplasia | Infantile Nephropathic Cystinosis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Alstrom Syndrome | Spinocerebellar Ataxia Type 40 | Adrenal Insufficiency | Thalassemia | Alzheimer Disease, Late Onset | Congenital Central Hypoventilation Syndrome | Hypertension, Essential | Coronary Restenosis | Achondrogenesis | Venous Insufficiency | Pyelonephritis | Schizophrenia | Porphyria, Variegate | Arthropathy | Congenital Bilateral Absence Of Vas Deferens | Cholesteryl Ester Storage Disease | Autosomal Recessive Congenital Ichthyosis | Hyperferritinemia-cataract Syndrome | Cirrhosis | Aneurysm, Thoracic Aortic | Primary Erythromelalgia | Metaphyseal Chondrodysplasia, Schmid Type | Hypotension, Orthostatic | Cardiac Sarcoidosis | Pneumothorax | Localized Scleroderma | Ventricular Septal Defect | Ebstein Anomaly | Poirier-Bienvenu Neurodevelopmental Syndrome | Aphasia | Spinocerebellar Ataxia Type 2 | Spinocerebellar Ataxia Type 27 | Kleine-Levin Syndrome | Epidermolysis Bullosa | Holt-Oram Syndrome | Melanoma | Branchiootorenal Syndrome | Hypospadias | Toxoplasmosis | Antiphospholipid Syndrome | Hepatitis C, Chronic | Long QT Syndrome Type 1 | Keratitis | Amenorrhea | Epidermodysplasia Verruciformis | Crisponi Syndrome | Turner's Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Osteonecrosis Of The Jaw | Crohn's Disease | Transient Bullous Dermolysis Of The Newborn | Binge Eating Disorder | Hypocalcemia | Pitt-Hopkins Syndrome | Hypotrichosis | Astrocytoma, Anaplastic | Cardiomyopathy, Peripartum | Exostoses | Cushing Syndrome | Hypertension, Renovascular | Hyperekplexia | Phosphoglycerate Dehydrogenase Deficiency | Hypohidrotic Ectodermal Dysplasia, X-linked | Hypotrichosis Simplex | Rheumatic Heart Disease | Oligoastrocytoma | Ophthalmia, Sympathetic | Mucolipidosis Type III | Spinocerebellar Ataxia Type 10 | Pulmonary Stenosis | Still Disease | Autoimmune Autonomic Ganglionopathy | Beare-Stevenson Syndrome | Primary Pigmented Nodular Adrenocortical Disease | Charcot-Marie-Tooth Disease Type 3 | Clouston Hidrotic Ectodermal Dysplasia | Duane Retraction Syndrome | 3-methylglutaconic Aciduria Type IV | Agoraphobia | Epilepsy Of Infancy With Migrating Focal Seizures | Dermatofibrosarcoma | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Cysticercosis | Chordoma | Hypohidrotic Ectodermal Dysplasia | Multiple Sclerosis | Oculocutaneous Albinism Type 1 | Polycystic Kidney, Autosomal Recessive | Coma | Sandhoff Disease | Hemochromatosis Type 2 | Neurofibromatosis Type 1 | DRESS Syndrome | LMNA-related Congenital Muscular Dystrophy | Waardenburg Syndrome Type 2E | Dyggve-Melchior-Clausen Disease | Vertigo | Keratoconjunctivitis | Microcephaly | Tardive Dyskinesia | Histoplasmosis | Cryopyrin-associated Periodic Syndromes | Biotinidase Deficiency | Coenzyme Q10 Deficiency | Chronic Leukemia | Oguchi Disease-2 | Homocystinuria | Hemorrhagic Disorders | Van Der Knaap Disease | Amelanotic Melanoma | Malonyl-CoA Decarboxylase Deficiency | Familial Episodic Pain Syndrome | Necrotizing Autoimmune Myopathy | Klippel-Feil Syndrome | Pelvic Inflammatory Disease | Multifocal Motor Neuropathy | Congenital Hemolytic Anemia | Arthritis | Choriocarcinoma | Idiopathic Pulmonary Fibrosis | Prediabetes | Glycogen Storage Disease Type 9 | VEXAS Syndrome | Hyperparathyroidism | Hereditary Sensory Neuropathy Type 1 | Cancer, Lung | Varices | Hypertensive Retinopathy | Malaria | Pseudohypoparathyroidism Type 1A | Corneal Dystrophies, Hereditary | Spondyloepiphyseal Dysplasia Tarda, X-linked | Agnathia-Otocephaly Complex | Early Infantile Epileptic Encephalopathy 13 | Familial Isolated Hyperparathyroidism | Proteasome-associated Autoinflammatory Syndrome 2 | Christianson Syndrome | Tyrosinemia Type 2 | Neurodermatitis | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Encephalopathy, Hepatic | Anorectal Malformations | Pheochromocytoma | Jaundice, Obstructive | Mitochondrial Encephalomyopathy | Dystonia | Hepatic Adenomatosis | Perivascular Epithelioid Cell Tumor | Epilepsy | Common Cold | Spondylo-ocular Syndrome | Depression | Juvenile Polyposis | Autosomal Recessive Bestrophinopathy | Klinefelter Syndrome | Retinal Diseases | Kallmann Syndrome | Inborn Errors Of Metabolism | Early Infantile Epileptic Encephalopathy 4 | Sengers Syndrome | Anodontia | Hartnup Disease | Leukoplakia, Oral | Metabolic Syndrome | Primary Lateral Sclerosis | Cabezas Syndrome | Pyruvate Dehydrogenase Deficiency | Smoldering Myeloma | Asplenia | Kawasaki Disease | Noonan Syndrome-like Disorder With Loose Anagen Hair | Familial Male-limited Precocious Puberty | Schizotypal Personality Disorder | Saethre-Chotzen Syndrome | Dysequilibrium Syndrome | Thromboembolism | Carbamoyl Phosphate Synthetase I Deficiency | Chromosome 9q34.3 Deletion Syndrome | Trigonocephaly | Cutaneous Angiosarcoma | Growth Hormone Excess | Abetalipoproteinemia | Gynecomastia | Lymphoma, B-cell | Waardenburg Syndrome | Birk-Barel Syndrome | Trichorhinophalangeal Syndrome | Glaucomatocyclitic Crisis | Ependymoma | Tremor | Autism | Tendinitis | Encephalocele | Gilbert Syndrome | Oculodentodigital Dysplasia | X-linked Acrogigantism | Spinocerebellar Ataxia Type 38 | Peripheral Neuropathy | Lateral Meningocele Syndrome | Trismus-pseudocamptodactyly Syndrome | LEOPARD Syndrome | Myosin Storage Myopathy | Schamberg Disease | Congenital Adrenal Hyperplasia | Renal Hypomagnesemia 3 | Endometrial Hyperplasia | Cohen Syndrome | Exocrine Pancreatic Insufficiency | Glycogen Storage Disease Type 1 | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Macrophage Activation Syndrome | Dysfibrinogenemia | Spinal Cord Diseases | Urticaria | Chylomicron Retention Disease | Chromosome 16p11.2 Deletion Syndrome | Obsessive-compulsive Disorder | Bursitis | Dwarfism | Delirium | IgA Nephropathy | DEND Syndrome | Neurodevelopmental Disorders | Persistent Truncus Arteriosus | Borjeson-Forssman-Lehmann Syndrome | Acute Tubular Necrosis | Fundus Albipunctatus | Trachoma | Usher Syndrome Type I | Stiff-man Syndrome | 3-methylglutaconic Aciduria Type I | Epidermolysis Bullosa Simplex, Generalized | Addison Disease | Atrial Septal Defect | Nephronophthisis | Heimler Syndrome | Centronuclear Myopathy | Congenital Absence Of Vas Deferens | Corneal Edema | Hyperglycemia | Proctitis | Alagille Syndrome | Anti-NMDA Receptor Encephalitis | Hemolytic Uremic Syndrome | Kabuki Syndrome | Wolfram Syndrome 2 | Colitis, Microscopic | Combined Malonic And Methylmalonic Acidemia | Thyrotoxic Periodic Paralysis | Meningeal Melanocytoma | Osteitis | Cerebrovascular Disorders | Angiodysplasia | Paraganglioma | Colitis, Lymphocytic | Congenital Disorders Of Glycosylation Type II | Nephroblastoma | Peutz-Jeghers Syndrome | Metachondromatosis | Apraxia | Joubert Syndrome | GAPO Syndrome | Congenital Muscular Dystrophy | Pre-eclampsia | Usher Syndrome Type II | Evans Syndrome | Osteoporosis | Familial Cerebral Amyloid Angiopathy | Poretti-Boltshauser Syndrome | Isovaleric Acidemia | Sturge-Weber Syndrome | Arthritis, Reactive | Mixed Connective Tissue Disease | Antisocial Personality Disorder | Lymphangioma | Chediak-Higashi Syndrome | Eosinophilia | Fraser Syndrome | Oligodendroglioma | Pontocerebellar Hypoplasia Type 7 | Oculopharyngeal Muscular Dystrophy | Epicondylitis | Pleural Tuberculosis | Stickler Syndrome | Retinopathy Of Prematurity | Rothmund-Thomson Syndrome | Schaaf-Yang Syndrome | Inflammatory Bowel Disease | Proximal Symphalangism | Congenital Adrenal Hyperplasia 1 | Esotropia | Neurocutaneous Melanocytosis | Chitayat Syndrome | Nephrotic Syndrome Type 1 | Liver Failure | Hypertension | CDKL5 Deficiency Disorder | Angiosarcoma Of The Breast | Spermatocele | Lafora Disease | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Uveitis, Anterior | Gerstmann-Straussler-Scheinker Syndrome | Fetal Alcohol Syndrome | 5-oxoprolinase Deficiency | Pernicious Anemia | Charcot-Marie-Tooth Disease Type 4B1 | Pyruvate Decarboxylase Deficiency | Lymphoma | Osteogenesis Imperfecta Type VI | Motor Neuron Diseases | Hyperinsulinism-hyperammonemia Syndrome | Hypermethioninemia | Acute Motor Axonal Neuropathy | Vitelliform Macular Dystrophy | Uveitis | Anemia | Charcot-Marie-Tooth Disease Axonal Type 2N | Pregnancy, Ectopic | REM Sleep Behavior Disorder | Alexander Disease | Motion Sickness | Charcot-Marie-Tooth Disease, Type 2C | Renal-hepatic-pancreatic Dysplasia | Congenital Stromal Corneal Dystrophy | Gliosarcoma | Spinocerebellar Ataxia Type 21 | Infantile Neuroaxonal Dystrophy | HELLP Syndrome | 3C Syndrome | Rubinstein-Taybi Syndrome | Sarcoma, Endometrial Stromal | Carbohydrate Metabolism Disorders | Limb Girdle Muscular Dystrophy | Infertility, Male | Eczema | Premenstrual Syndrome | Recurrent Respiratory Papillomatosis | Lymphopenia | Aicardi-Goutieres Syndrome | Alpha-1 Antitrypsin Deficiency | Scleroderma, Diffuse | Keratosis, Actinic | Spinocerebellar Ataxia Type 12 | Progressive Encephalopathy-optic Atrophy Syndrome | Mast Cell Leukemia | Spinocerebellar Ataxia Type 3 | Stroke, Hemorrhagic | X-linked Charcot-Marie-Tooth Disease | Congenital Diaphragmatic Hernia | Chronic Idiopathic Myelofibrosis | Lymphedema-distichiasis Syndrome | Cystinuria | Pityriasis Rubra Pilaris | Meningioma, Benign | Opisthorchiasis | Myofibrillar Myopathy | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Thalassemia, Beta | Multiple Sulfatase Deficiency | Sleep Apnea, Obstructive | Colorectal Adenoma | Hypoplastic Left Heart Syndrome | Hyperthyroidism | Congenital Aniridia | Scapuloperoneal Spinal Muscular Atrophy | Erysipelas | X-linked Creatine Transporter Deficiency | Polycythemia Vera | Patent Ductus Arteriosus | Congenital Myopathy | Cavitary Optic Disc Anomalies | Intestinal Obstruction