Intestinal Pseudo-obstruction

About the Disease
Congenital Short Bowel Syndrome, also known as congenital short bowel, is related to intestinal pseudo-obstruction and short bowel syndrome. An important gene associated with Congenital Short Bowel Syndrome is CLMP (CXADR Like Membrane Protein). The drugs Prucalopride and Gastrointestinal Agents have been mentioned in the context of this disorder. Affiliated tissues include small intestine, liver and kidney, and related phenotypes are intestinal hypoplasia and short stature

Common Targets
MYH11 | HTR4 | FLNA | TFAP2B | ACTG2 | MLNR | LMOD1

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

Other Diseases

Congenital Hereditary Endothelial Dystrophy Type I | Burn-McKeown Syndrome | Polycythemia | Diffuse Palmoplantar Keratoderma | Congenital Diaphragmatic Hernia | Leigh Syndrome | Neuropathy | Metabolic Syndrome | Diabetes Insipidus, Nephrogenic | Basal Ganglia Cerebrovascular Disease | Prader-Willi Syndrome | Delayed Sleep Phase Syndrome | Oligodendroglioma | Intellectual Disability, Autosomal Dominant 5 | Empyema | Nephropathy | Lesch-Nyhan Syndrome | Cellulitis | Intestinal Obstruction | Inborn Errors Of Metabolism | DEND Syndrome | Cutis Laxa | GLUT1 Deficiency Syndrome | Carney-Stratakis Syndrome | Autosomal Recessive Congenital Ichthyosis | Angina Pectoris | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Polymyositis | Leukoplakia | Ameloblastoma | Inflammatory Myofibroblastic Tumor | Renal-hepatic-pancreatic Dysplasia | Loeys-Dietz Syndrome Type 4 | Polymyalgia Rheumatica | Vitreoretinal Degeneration, Snowflake Type | Bladder Exstrophy | Intestinal Hypomagnesemia 1 | Benign Familial Infantile Seizures | PHARC Syndrome | Camptocormia | Inflammatory Bowel Disease | Trichorhinophalangeal Syndrome | Still Disease | Weill-Marchesani Syndrome | Malnutrition | Osteomalacia | Hydrocephalus, Normal Pressure | Insulinoma | Vertigo | Macrodactyly | Hyperparathyroidism, Secondary | Basal Ganglia Disease | Allergic Contact Dermatitis | Fanconi Anemia | Temtamy Preaxial Brachydactyly Syndrome | Hypermethioninemia | Liver Failure, Acute Infantile | Sleep Disorder | Vasculitis | Panniculitis | Olmsted Syndrome | Autoimmune Polyendocrinopathy Syndrome Type I | Lyme Disease | Liebenberg Syndrome | Werner's Syndrome | Primary Biliary Cholangitis | Pulmonary Tuberculosis | Schizophrenia | LRBA Deficiency | Micropenis | Cholestasis, Intrahepatic | Thanatophoric Dysplasia Type 1 | Large Granular Lymphocytic Leukemia | Multiple Sulfatase Deficiency | Epithelial-myoepithelial Carcinoma | Spinocerebellar Ataxia Type 31 | Microtia | Extramammary Paget's Disease | Sleep Apnea | HUPRA Syndrome | Choriocarcinoma | Frontotemporal Dementia | Chronic Granulomatous Disease, X-linked | Proctitis | Osteoglophonic Dysplasia | Scabies | Dengue Shock Syndrome | Hypothalamic Obesity | Spinocerebellar Ataxia Type 3 | Proteasome-associated Autoinflammatory Syndrome 2 | Motor Neuron Diseases | X-linked Sideroblastic Anemia | Glaucoma | Conduct Disorder | Pelizaeus-Merzbacher Disease | VEXAS Syndrome | Multiple Sclerosis, Secondary Progressive | Spitz Nevus | Myocardial Infarction | Thalassemia | Spinocerebellar Ataxia Type 2 | Herpes Simplex Dermatitis | Iron Overload | Liddle Syndrome | Temporal Lobe Epilepsy | Dermatitis | Hairy Cell Leukemia | Richter's Syndrome | Facioscapulohumeral Muscular Dystrophy | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Sensorineural Hearing Loss | Muir-Torre Syndrome | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Mountain Sickness | Heavy Chain Disease | Neuroendocrine Cancer | Hyperglycemia | Chronic Granulomatous Disease | Exotropia | Long QT Syndrome Type 2 | Acromesomelic Dysplasia | Retinitis Pigmentosa | Multiple Sclerosis, Primary Progressive | Apraxia | Cold Agglutinin Disease | Antithrombin III Deficiency | Osteopathia Striata With Cranial Sclerosis | Primary Aldosteronism | Lafora Disease | Craniopharyngioma | Vaginitis | Giant Axonal Neuropathy | Spinocerebellar Ataxia Type 5 | Conjunctivitis | Chromosome 16p11.2 Deletion Syndrome | Congenital Generalized Lipodystrophy | Fetal Akinesia Deformation Sequence | Crigler-Najjar Syndrome | Tangier Disease | Spinocerebellar Ataxia Type 20 | Chondrodysplasia Punctata 1, X-linked Recessive | Common Variable Immunodeficiency | Juvenile Myoclonic Epilepsy | Neutropenia | Neuromyotonia | Smoldering Myeloma | Premature Ejaculation | KBG Syndrome | Chorea | Alpha-mannosidosis | Carbonic Anhydrase VA Deficiency | Postpartum Depression | Coronary Restenosis | Wiedemann-Steiner Syndrome | Nasodigitoacoustic Syndrome | Graft-versus-host Disease | Alzheimer Disease, Late Onset | Behavioral Variant Of Frontotemporal Dementia | Raine Syndrome | Exostoses | Nemaline Myopathy 8 | Non-bullous Congenital Ichthyosiform Erythroderma | Neurofibromatosis | Aspergillosis | Cervicitis | Progressive Familial Intrahepatic Cholestasis Type 3 | Adenoma, Pituitary | Carcinoid Syndrome | Chorioretinitis | Spinocerebellar Ataxia Type 15 | Liver Diseases | Urofacial Syndrome | Pseudoachondroplasia | Thyrotoxic Periodic Paralysis | Cancer, Brain | Seizures | Multiple Sclerosis, Chronic Progressive | Epilepsy, Generalized | Hyperbilirubinemia | Orthostatic Intolerance | Spondylocostal Dysostosis | Vitamin B12 Deficiency | Sick Sinus Syndrome 1 | Porphyria, Acute Intermittent | Short-chain Acyl-CoA Dehydrogenase Deficiency | Nemaline Myopathy 10 | Cone Dystrophy | Fahr Disease | Melanoma, Uveal | Charcot-Marie-Tooth Disease, Type 2C | Aplastic Anemia | Dengue Hemorrhagic Fever | Eczema | Pyruvate Kinase Deficiency | Pineoblastoma | Zimmermann-Laband Syndrome | Cornelia De Lange Syndrome | Colitis, Microscopic | Arthrogryposis | Pulmonary Alveolar Proteinosis | Progressive External Ophthalmoplegia | Bipolar Disorder | Apert Syndrome | Goiter, Nodular | Palsy, Cerebral | Spinal Muscular Atrophy Type 3 | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Nephrotic Syndrome Type 1 | Creutzfeldt-Jakob Disease | Wilson's Disease | Roberts Syndrome | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Mucolipidosis Type II | ICF Syndrome | Hereditary Sensory Neuropathy Type 1 | Papillorenal Syndrome | T-cell Chronic Lymphocytic Leukemia | Hidradenitis Suppurativa | Glutaric Aciduria Type 3 | Paget's Disease Of The Breast | Hemorrhage | Autoimmune Polyendocrine Syndrome | Erythema Nodosum | Hemorrhagic Disorders | Kearns-Sayre Syndrome | Stuttering | Infantile Neuroaxonal Dystrophy | McKusick Type Metaphyseal Chondrodysplasia | Anal Fissure | Schistosomiasis Mansoni | Congenital Primary Aphakia | Adenosine Deaminase Deficiency | Huntington's Disease | Schwannomatosis | Hepatitis A | Herpes Genitalis | Focal Segmental Glomerulosclerosis | Atelosteogenesis Type 1 | Vitreoretinopathy, Proliferative | Cirrhosis | Autosomal Recessive Bestrophinopathy | Mitochondrial DNA Depletion Syndrome 13 | Gestational Trophoblastic Disease | Myasthenia | Skin Papilloma | Retinal Telangiectasia | Pupil Disorders | Congenital Heart Defects | Mesothelioma, Malignant | Coffin-Lowry Syndrome | Nemaline Myopathy | Tyrosinemia Type 2 | Gyrate Atrophy Of The Choroid And Retina | Fibromuscular Dysplasia | Isovaleric Acidemia | Cri-du-chat Syndrome | Pontocerebellar Hypoplasia Type 2 | Glioblastoma Multiforme | Carcinoma, Signet Ring Cell | Li-Fraumeni Syndrome | Ophthalmoplegia | Benign Familial Neonatal Convulsions | Acrocallosal Syndrome | Renal Hypouricemia | Down Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Myofibrillar Myopathy | Spinocerebellar Ataxia Type 40 | Astigmatism | Pyruvate Decarboxylase Deficiency | Mucolipidosis Type IV | Cystinosis | Uveitis | Metatropic Dysplasia | Urea Cycle Disorder | Cancer, Colon | Intracranial Hypertension | Familial Male-limited Precocious Puberty | Familial Digital Arthropathy-brachydactyly | Hyperekplexia | Keratosis | Charcot-Marie-Tooth Disease Type 2D | Demyelinating Diseases | Lentigo | Acute Generalized Exanthematous Pustulosis | Pelvic Inflammatory Disease | Guttate Psoriasis | Porphyria Cutanea Tarda | Trismus-pseudocamptodactyly Syndrome | Norrie Disease | Congenital Disorders Of Glycosylation | Erythrokeratodermia Variabilis | Occipital Neuralgia | Hypotonia-cystinuria Syndrome | Chromosome 5q Deletion Syndrome | Neurotoxicity | Primary Pigmented Nodular Adrenocortical Disease | Rhizomelic Chondrodysplasia Punctata | Hypercalcemia | Spinocerebellar Ataxia Type 21 | Rolandic Epilepsy | Priapism | Spinocerebellar Ataxia Type 23 | Spinal Cord Diseases | Shprintzen-Goldberg Syndrome | Mitochondrial Cytopathy | Ichthyosis, X-linked | Marshall-Smith Syndrome | Cardiac Arrest | Neuroleptic Malignant Syndrome | Glomerulonephritis | Pneumothorax | Myofibromatosis | Pneumoconiosis | Hemangioma | Huntington's Disease-like 2 | Citrullinemia | Oral Lichen Planus | Atelosteogenesis Type 2 | Progressive Familial Intrahepatic Cholestasis | Coronary Heart Disease | Depression | Papilloma | Spinocerebellar Ataxia Type 16 | Spina Bifida | Restrictive Dermopathy | Paroxysmal Kinesigenic Dyskinesia | Alveolar Capillary Dysplasia | Cabezas Syndrome | Periventricular Leukomalacia | Tonsillitis | Tardive Dyskinesia | Neonatal Progeroid Syndrome | Amelanotic Melanoma | Neuromyelitis Optica | Warsaw Breakage Syndrome | Familial Hemiplegic Migraine | Lichen Planus | AIDS Dementia Complex | Axenfeld-Rieger Syndrome | Congenital Aniridia | Eclampsia | Tay-Sachs Disease | Eating Disorder | Narcolepsy | Meier-Gorlin Syndrome | Acute Lymphocytic Leukemia | Thrombophlebitis | Cerebrovascular Disorders | Ornithine Transcarbamylase Deficiency | Nanophthalmos | Bartter Syndrome | Hemimegalencephaly | Hyperferritinemia-cataract Syndrome | Meleda Disease | Hoyeraal-Hreidarsson Syndrome | Chronic Myeloid Leukemia | Long QT Syndrome Type 3 | Lathosterolosis | Hypoproteinemia, Hypercatabolic | Distal Myopathy | Craniometaphyseal Dysplasia | Carcinoma, Transitional Cell | Persistent Mullerian Duct Syndrome | Spinocerebellar Ataxia Type 7 | Absence Epilepsy | Eosinophilic Asthma | Epidermolysis Bullosa | Tyrosinemia Type 1 | NGLY1 Deficiency | Takotsubo Cardiomyopathy | Osteogenesis Imperfecta Type VI | Stiff-man Syndrome | Neuroma | Waardenburg Syndrome Type 1 | Oculocutaneous Albinism Type 1 | Abetalipoproteinemia | Erythema Multiforme | Mood Disorder | Hereditary Pyropoikilocytosis | Myelofibrosis | Myoclonic Atonic Epilepsy | Blomstrand Osteochondrodysplasia | Neovascular Glaucoma | Dystonia Musculorum Deformans | Acromicric Dysplasia | Hypokalemia | Neurocysticercosis | Chondroma | Myocarditis | Retinitis | Hypobetalipoproteinemias | Aarskog-Scott Syndrome | Rheumatoid Arthritis | Osteogenesis Imperfecta Type V | Meningioma, Benign | Familial Retinal Arterial Macroaneurysm | Traboulsi Syndrome | Prurigo Nodularis | Pulmonary Sclerosing Hemangioma