Disease

Meconium Ileus

About the Disease
Meconium Ileus, also known as intestinal obstruction in the newborn due to guanylate cyclase 2c deficiency, is related to duodenal atresia and cystic fibrosis, modifier of, 1, and has symptoms including bowel spasm and gastric distention. An important gene associated with Meconium Ileus is GUCY2C (Guanylate Cyclase 2C). The drugs Sodium citrate and Fentanyl have been mentioned in the context of this disorder. Affiliated tissues include colon, liver and small intestine, and related phenotypes are microcolon and meconium ileus

Common Targets
NOS1 | GUCY2C | TGFB1 | MSRA

疾病靶点研报
Meconium Ileus

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

Other Diseases

Muscular Dystrophy | Martsolf Syndrome | Hypotrichosis Simplex | Sarcoma, Ewing | Hepatoblastoma | Porencephaly | Meningitis | Overactive Bladder | Hemophilia | Waardenburg Syndrome Type 4A | Shwachman-Bodian-Diamond Syndrome | Leishmaniasis, Cutaneous | Sleep Apnea, Central | Vitamin B12 Deficiency | Fundus Albipunctatus | Renal Tubular Dysgenesis | Pericarditis | Kawasaki Disease | Charcot-Marie-Tooth Disease Type 4D | Crigler-Najjar Syndrome | Photosensitivity | Pulmonary Alveolar Microlithiasis | Twin-to-twin Transfusion Syndrome | Stromal Corneal Dystrophy | Primary Hyperoxaluria Type 1 | Hepatopulmonary Syndrome | GM2-gangliosidosis AB Variant | Erysipelas | Carcinoid Tumor | Barakat Syndrome | Glycogen Storage Disease Type 9 | Large Granular Lymphocytic Leukemia | Plasma Cell Leukemia | Spinocerebellar Ataxia Type 15 | Jalili Syndrome | Multiple Sclerosis, Secondary Progressive | Adenosine Deaminase 2 Deficiency | Chromosome 9q34.3 Deletion Syndrome | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Pemphigus Foliaceus | Peroxisomal Disorder | Infantile Neuroaxonal Dystrophy | MELAS Syndrome | Hypertension, Renal | Episodic Ataxia | Hypospadias | Parvovirus B19 Infection | Hypopituitarism | Dubin-Johnson Syndrome | Obsessive-compulsive Disorder | Bladder Exstrophy | Adenoma, Villous | Scleritis | Dermatofibrosarcoma | Hemolytic Anemia | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Ophthalmia, Sympathetic | Eiken Syndrome | Familial Male-limited Precocious Puberty | Cleidocranial Dysplasia | Guillain-Barre Syndrome | Pelvic Inflammatory Disease | Klippel-Feil Syndrome | Congenital Dysfibrinogenemia | Centronuclear Myopathy | Argininosuccinic Aciduria | CREST Syndrome | Presbyopia | Polycystic Kidney, Autosomal Dominant | Systemic Mastocytosis | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Microcephaly | Lymphoma, AIDS-related | Spinocerebellar Ataxia Type 16 | Dent Disease | Joubert Syndrome | Endophthalmitis | 3-methylglutaconic Aciduria | Schuurs-Hoeijmakers Syndrome | Agammaglobulinemia | Mabry Syndrome | Hypertension, Essential | Meckel-Gruber Syndrome | Pemphigus Vulgaris | Microcephalic Primordial Dwarfism | Myelomeningocele | Pityriasis Rubra Pilaris | Pneumothorax | Cutaneous T-cell Lymphoma | Duane Retraction Syndrome | Macrophagic Myofasciitis | Migraine | Lesch-Nyhan Syndrome | Hyperinsulinemic Hypoglycemia | Osteochondroma | Angelman Syndrome | Carpal Tunnel Syndrome | Purpura, Thrombotic Thrombocytopenic | Glanzmann Thrombasthenia | Pompe Disease | Juvenile Myelomonocytic Leukemia | Sarcoidosis, Pulmonary | Pulmonary Vein Stenosis | Malnutrition | Blau Syndrome | Spinocerebellar Ataxia Type 1 | Gilbert Syndrome | Metanephric Adenoma | Dwarfism | Warsaw Breakage Syndrome | Charcot-Marie-Tooth Disease Type 3 | Pendred Syndrome | Camurati-Engelmann Disease | Epidermal Nevus Syndrome | Nestor-Guillermo Progeria Syndrome | Okihiro Syndrome | Lafora Disease | Hypotonia-cystinuria Syndrome | Alexander Disease | Hypereosinophilic Syndrome | Transcobalamin Deficiency | Methylmalonic Acidemia | Hepatitis | Microcephaly, Seizures, And Developmental Delay | Esophageal Carcinoma | Neuroleptic Malignant Syndrome | Ameloblastoma | Persistent Hyperplastic Primary Vitreous | Pyruvate Carboxylase Deficiency Disease | Schnyder Crystalline Corneal Dystrophy | Fibrodysplasia Ossificans Progressiva | Pure Autonomic Failure | Retinal Degeneration | Congenital Myopathy | Farber Disease | Familial Hemiplegic Migraine | Spinocerebellar Ataxia Type 10 | Hypervalinemia | Depression | Pleurisy | Papulopustular Rosacea | Hartsfield Syndrome | Combined Malonic And Methylmalonic Acidemia | Specific Granule Deficiency | Coenzyme Q10 Deficiency | Bulimia Nervosa | Fetal And Neonatal Alloimmune Thrombocytopenia | Androgenic Alopecia | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Seasonal Mood Disorder | Panniculitis | Onchocerciasis | Chronic Beryllium Disease | Sleep Apnea | GNE Myopathy | Mucolipidosis | Thyroid Dyshormonogenesis | Mycosis Fungoides | Hemochromatosis | Cholestasis, Intrahepatic | Autoimmune Disease | Congenital Poikiloderma | Acrodysostosis | Heterotaxy | Oculocutaneous Albinism Type 4 | Thin Basement Membrane Disease | Hyperkeratosis | Pycnodysostosis | Ehlers-Danlos Syndrome | Primary Hyperoxaluria Type 3 | Holoprosencephaly | Colitis, Lymphocytic | Cri-du-chat Syndrome | Delirium | Craniosynostosis | Early Infantile Epileptic Encephalopathy 28 | Encephalopathy, Glycine | Usher Syndrome Type III | Porphyria, Acute Intermittent | Parkinson's Disease | Measles | Malignant Peripheral Nerve Sheath Tumor | GATA2 Deficiency | Central Core Disease | Mitochondrial DNA Depletion Syndrome | Triple A Syndrome | Inborn Errors Of Metabolism | Pontocerebellar Hypoplasia Type 2 | Histiocytic Sarcoma | Thyroiditis | Oligoasthenoteratozoospermia | Hemophagocytic Lymphohistiocytosis | Cyclic Vomiting Syndrome | Immunoproliferative Disorders | Familial Mediterranean Fever | Diabetes Gestational | Wagner Disease | Paraplegia | Pulmonary Sclerosing Hemangioma | Mesothelioma, Malignant | Pseudohermaphroditism | Poretti-Boltshauser Syndrome | Hepatitis E | Alkaptonuria | Brugada Syndrome 1 | Batten Disease | Costello Syndrome | Distal Myopathy | Mandibuloacral Dysplasia With Type A Lipodystrophy | Iron Metabolism Disorders | Leukemia-lymphoma, Adult T-cell | Growth Hormone Excess | Nance-Horan Syndrome | Retinal Diseases | Cholera | Cardiospondylocarpofacial Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Spinal Muscular Atrophy | Huntington's Disease | Charcot-Marie-Tooth Disease, Type 1A | High Molecular Weight Kininogen Deficiency | Contact Dermatitis | Renal Medullary Carcinoma | Ganglioglioma | Cholestasis | Leukemia | Juvenile Myoclonic Epilepsy | Carbonic Anhydrase VA Deficiency | Progressive Familial Intrahepatic Cholestasis Type 2 | Exocrine Pancreatic Insufficiency | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Hypercalciuria | Pituitary Disorders | Myelodysplasia | Toxoplasmosis | Hypertrophy | Chordoma | Spinocerebellar Ataxia Type 5 | ACTH-independent Macronodular Adrenal Hyperplasia | Occipital Neuralgia | Psoriasis | Nanophthalmos | Osteosarcoma | Still Disease | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Melanoma, Uveal | Nutrition Disorders | Cornelia De Lange Syndrome | Nasodigitoacoustic Syndrome | Hoyeraal-Hreidarsson Syndrome | Sialoadenitis | Blepharophimosis Syndrome | Gastric Atrophy | Eclampsia | Feingold Syndrome | Hypothalamic Obesity | Short-chain Acyl-CoA Dehydrogenase Deficiency | Acute Kidney Injury | Otosclerosis | Nephritis, Interstitial | Progressive Familial Intrahepatic Cholestasis Type 1 | Hypertension, Pulmonary | Spinocerebellar Ataxia Type 2 | Encephalitis, Tick-borne | Vogt-Koyanagi-Harada Syndrome | Spondylo-ocular Syndrome | Subcortical Band Heterotopia | Tietze Syndrome | Restless Legs Syndrome | Erythematotelangiectatic Rosacea | Chondroma | Tularemia | Sensory Neuropathy | Hypogonadism | Trichothiodystrophy | Hypophosphatasia | Polyradiculopathy | Facioscapulohumeral Muscular Dystrophy | IgA Nephropathy | Nicotine Addiction | Diabetes | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Seizures-scoliosis-macrocephaly Syndrome | Antenatal Bartter Syndrome Type 1 | Periventricular Nodular Heterotopia | Lung Diseases | Absence Epilepsy | Rosacea | Epilepsy, Generalized | Epidermolytic Palmoplantar Keratoderma | Atelosteogenesis Type 1 | Pseudohypoparathyroidism Type 2 | Leukoencephalopathy, Progressive Multifocal | Spinocerebellar Ataxia Type 17 | Primary Progressive Nonfluent Aphasia | Hepatitis, Chronic | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Cyst | Myelitis, Transverse | Osteopetrosis | Sepiapterin Reductase Deficiency | Scleroderma, Diffuse | Wolman Disease | Amyotrophic Lateral Sclerosis | X-linked Acrogigantism | Atopic Dermatitis | Epithelioid Hemangioma | Triphalangeal Thumb-polysyndactyly Syndrome | Japanese Encephalitis | Stickler Syndrome | Familial Episodic Pain Syndrome | LMNA-related Congenital Muscular Dystrophy | Shock, Cardiogenic | Schamberg Disease | Impetigo | Leukocyte Adhesion Deficiency Type 1 | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Paroxysmal Nocturnal Hemoglobinuria | Down Syndrome | Tuberculous Meningitis | Amelanotic Melanoma | Familial Hyperaldosteronism | Retinal Detachment | VEXAS Syndrome | Episodic Ataxia Type 1 | Stomatitis | Chronic Granulomatous Disease, X-linked | Craniofrontonasal Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | TARP Syndrome | Alpers Syndrome | Bicuspid Aortic Valve | Castleman Disease | Long QT Syndrome Type 2 | Glomerulonephritis, Membranous | Hepatitis A | Olmsted Syndrome | Vitamin D Deficiency | Hyperostosis | Hemangioblastoma | Spina Bifida | Lysosomal Acid Lipase Deficiency | Amish Infantile Epilepsy Syndrome | Early Infantile Epileptic Encephalopathy 4 | Sialidosis | Anal Fissure | Pierre Robin Syndrome | Retinopathy, Diabetic | Corneal Neovascularization | Familial Thoracic Aortic Aneurysm | Hypocalcemia | Myosin Storage Myopathy | Charcot-Marie-Tooth Disease Type 4 | Thalassemia | Von Hippel-Lindau Disease | Calcium Pyrophosphate Deposition Disease | Congenital Torticollis | Familial Digital Arthropathy-brachydactyly | Optic Neuropathy, Anterior Ischemic | Diffuse Intrinsic Pontine Glioma | Spinal Cord Diseases | Gnathodiaphyseal Dysplasia | Periodic Limb Movement Disorder | Myoclonus-dystonia Syndrome | Adenoma, Pituitary | Pancreatitis, Chronic | Aneurysm, Abdominal Aortic | Eosinophilic Asthma | Fibronectin Glomerulopathy | Protein C Deficiency | Rubinstein-Taybi Syndrome | Urea Cycle Disorder | Anthrax | Leukoplakia, Oral | Epicondylitis | Renal Hypouricemia | Cholecystitis | Rhizomelic Chondrodysplasia Punctata | Tinea Versicolor | Retinal Dystrophy | Vaginitis | Toxic Epidermal Necrolysis | Hemorrhagic Disorders | Takotsubo Cardiomyopathy | CDKL5 Deficiency Disorder | Premature Ejaculation | Erythema Multiforme | Rothmund-Thomson Syndrome | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Progressive Familial Intrahepatic Cholestasis Type 3 | Herpes Genitalis | Fibromyalgia | LRBA Deficiency | Aceruloplasminemia | Trichuriasis | Marfan Syndrome | Wolfram Syndrome | DNA Ligase IV Deficiency | Esophagitis, Eosinophilic | Perivascular Epithelioid Cell Tumor