Disease

Exocrine Pancreatic Insufficiency

About the Disease
Exocrine Pancreatic Insufficiency is related to shwachman-diamond syndrome 1 and johanson-blizzard syndrome. An important gene associated with Exocrine Pancreatic Insufficiency is SCT (Secretin), and among its related pathways/superpathways are Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers and Type II diabetes mellitus. The drugs Glucagon and Dulaglutide have been mentioned in the context of this disorder. Affiliated tissues include Pancreas, liver and bone marrow, and related phenotypes are no effect and no effect

Common Targets
GSK3B | CELA1 | SPINK1 | TGFB1

疾病靶点研报
Exocrine Pancreatic Insufficiency

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

Other Diseases

Charcot-Marie-Tooth Disease, Type 1A | Otopalatodigital Syndrome Type 2 | Meniere's Disease | Pemphigus Vulgaris | Thalassemia | Sclerocornea | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Systemic Mastocytosis | Cabezas Syndrome | CEDNIK Syndrome | Melnick-Needles Syndrome | Carey-Fineman-Ziter Syndrome | L-2-Hydroxyglutaric Aciduria | Unverricht-Lundborg Syndrome | Hemolytic Uremic Syndrome, Atypical | Congenital Poikiloderma | Aspergillosis | Microtia | Methylmalonic Aciduria And Homocystinuria, CblC Type | Autoimmune Autonomic Ganglionopathy | Maple Syrup Urine Disease | Congenital Myopathy | Chorea-acanthocytosis | Blepharo-cheilo-odontic Syndrome | Platelet Disorders | Focal Cortical Dysplasia Type 2 | Amyotrophic Lateral Sclerosis | Polymyalgia Rheumatica | Robinow Syndrome | Lysosomal Acid Lipase Deficiency | Retinoschisis | Hemangioendothelioma | Myelomeningocele | Cataract | Porphyria Cutanea Tarda | Joubert Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Congenital Mirror Movements | Guanidinoacetate Methyltransferase Deficiency | Glomerulonephritis, Membranoproliferative | Cold Agglutinin Disease | Temtamy Preaxial Brachydactyly Syndrome | Diffuse Intrinsic Pontine Glioma | Familial Hemiplegic Migraine | Fibrosarcoma | Pyoderma Gangrenosum | Apert Syndrome | Encephalopathy, Hepatic | Chiari Malformation Type I | Glycogen Storage Disease Type 0, Muscle | Hyperprolactinemia | Prolymphocytic Leukemia | Budd-Chiari Syndrome | Hyperuricemia | Antenatal Bartter Syndrome Type 1 | Mountain Sickness | Multiple Myeloma | Tyrosinemia | Triple A Syndrome | Chronic Myeloid Leukemia | Colitis, Microscopic | Glycogen Storage Disease Type 1 | Hoyeraal-Hreidarsson Syndrome | Epidermal Nevus Syndrome | Anorexia Nervosa | Crisponi Syndrome | Renal Medullary Carcinoma | Mucolipidosis Type III | Osteitis | Synpolydactyly | Neurocysticercosis | Silicosis | Iron Overload | Spinocerebellar Ataxia Type 38 | Immunoproliferative Disorders | Esotropia | Early Infantile Epileptic Encephalopathy 28 | Rhabdomyosarcoma, Embryonal | Uremic Pruritus | Wolfram Syndrome | Relapsing Polychondritis | Shock, Cardiogenic | Dengue Hemorrhagic Fever | Charcot-Marie-Tooth Disease, Type 2A | Long QT Syndrome Type 3 | Pyloric Stenosis, Infantile Hypertrophic | B-cell Prolymphocytic Leukemia | Parkinson Disease 6, Autosomal Recessive Early-onset | Carney Triad | Blastoma, Pleuropulmonary | Cyst | Familial Digital Arthropathy-brachydactyly | Prurigo Nodularis | Lathosterolosis | Common Cold | Congenital Bilateral Absence Of Vas Deferens | Spinal Muscular Atrophy Type 3 | Impetigo | Early Infantile Epileptic Encephalopathy 4 | Cholangiocarcinoma | Ellis-Van Creveld Syndrome | Addison Disease | Crimean-Congo Hemorrhagic Fever | Rhabdomyosarcoma, Alveolar | Extramammary Paget's Disease | Hypodontia | Spinocerebellar Ataxia Type 10 | Orthostatic Intolerance | Pathological Gambling | Spinal And Bulbar Muscular Atrophy | Yellow Fever | Chloridorrhea, Congenital | Double Outlet Right Ventricle | Pseudohypoaldosteronism | Congenital Nystagmus | Pernicious Anemia | Multiple Sclerosis, Secondary Progressive | Hyperparathyroidism | Distal Spinal Muscular Atrophy | Amyloidosis | Lissencephaly 2 | Acrocallosal Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Neurodermatitis | Takenouchi-Kosaki Syndrome | Myocardial Infarction | Adenomyosis | Acromicric Dysplasia | Periodontitis | Dyggve-Melchior-Clausen Disease | Shwachman-Bodian-Diamond Syndrome | Acute Anterior Uveitis | Erdheim-Chester Disease | Ichthyosis | Dowling-Degos Disease | Corneal Neovascularization | Craniofrontonasal Syndrome | Purpura, Thrombotic Thrombocytopenic | Anthrax | Microvillus Inclusion Disease | Sensorineural Hearing Loss | Coronary Restenosis | Joubert Syndrome 2 | Acromegaly | Acral Lentiginous Melanoma | Familial Glucocorticoid Deficiency | Hereditary Folate Malabsorption | Seizures | Acute Chest Syndrome | Dysthymia | Intermittent Claudication | Borjeson-Forssman-Lehmann Syndrome | Colitis, Lymphocytic | Pseudohypoparathyroidism Type 2 | Oculocutaneous Albinism | Charcot-Marie-Tooth Disease Type 2D | Neuroblastoma | Chronic Lymphocytic Leukemia | Progressive External Ophthalmoplegia | Lupus Erythematosus | Congenital Generalized Lipodystrophy | Waardenburg Syndrome Type 4A | Zollinger-Ellison Syndrome | Influenza | Idiopathic Pulmonary Fibrosis | Erectile Dysfunction | Fanconi Anemia | Vitamin D Deficiency | Pompe Disease | Tic Disorder | Cataplexy | Palsy, Cerebral | Triphalangeal Thumb-polysyndactyly Syndrome | Primary Sclerosing Cholangitis | Primary Hyperoxaluria Type 1 | Polymyositis | Arthrogryposis | Purpura | Jalili Syndrome | Sarcosinemia | Cornelia De Lange Syndrome | Meningitis | Barrett Esophagus | Hereditary Spastic Paraplegia | Bullous Pemphigoid | Hypospadias | Arterial Tortuosity Syndrome | Spinocerebellar Ataxia Type 12 | Glutaric Aciduria Type 2 | Hypertelorism | Congenital Stationary Night Blindness | Diamond-Blackfan Anemia | Postpoliomyelitis Syndrome | Congenital Lipoid Adrenal Hyperplasia | Conjunctivitis, Allergic | Renal Failure | Polycystic Liver | Erythromelalgia | Congenital Hemolytic Anemia | Peritonitis | Spinocerebellar Ataxia Type 20 | Oligoasthenoteratozoospermia | Central Pain Syndrome | Heterotaxy | Presbycusis | Bethlem Myopathy | Diabetes Type 1 | Precocious Puberty | Esophagitis | Hypoplastic Left Heart Syndrome | Bernard-Soulier Syndrome | Eiken Syndrome | Diabetes Insipidus, Neurogenic | Stuttering | Primary Familial Brain Calcification | Pigment Dispersion Syndrome | Primrose Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Orotic Aciduria | Fibromyalgia | Borderline Personality Disorder | Creatine Deficiency Syndrome | Marinesco-Sjogren Syndrome | Usher Syndrome Type III | Blomstrand Osteochondrodysplasia | Leukemia | Agoraphobia | Meier-Gorlin Syndrome | Alpha-1 Antitrypsin Deficiency | Hyperkeratosis | Dystonia Musculorum Deformans | Dental Caries | Hypoglycemia | Pseudohypoparathyroidism Type 1C | Schindler Disease | Chorea | Majeed Syndrome | Sorsby Fundus Dystrophy | Sarcoma, Alveolar Soft Part | Usher Syndrome | Intracerebral Hemorrhage | Metatropic Dysplasia | Osteonecrosis Of The Jaw | Congenital Adrenal Hyperplasia | Pancreatitis | Gastroenteritis, Eosinophilic | Cold-induced Sweating Syndrome | Viral Meningitis | Keratosis | Myoclonus-dystonia Syndrome | Blue Nevus | Pituitary Dwarfism | Low Tension Glaucoma | Hypertrophy | Perivascular Epithelioid Cell Tumor | Corneal Dystrophy | Antisynthetase Syndrome | Myeloid Leukemia | Peroxisomal Disorder | HUPRA Syndrome | Pupil Disorders | Thrombocytopenia | Renal Oncocytoma | Retinal Diseases | Fibrillation, Atrial | Leukemia-lymphoma, Adult T-cell | Stargardt Disease | Dyslexia | Cyclic Vomiting Syndrome | Stevens-Johnson Syndrome | Acute Leukemia | Phenylketonuria II | Malaria, Cerebral | Congenital Hereditary Endothelial Dystrophy Type II | Goiter, Nodular | Sialidosis Type I | Muscle Wasting | Tay-Sachs Disease | Congenital Dyserythropoietic Anemia | Meningioma, Benign | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Pierpont Syndrome | Cranioectodermal Dysplasia | Transcobalamin Deficiency | Tylosis With Esophageal Cancer | Spinocerebellar Ataxia Type 2 | Asthma | Patent Foramen Ovale | Rubeosis Iridis | Hypotension, Orthostatic | Renal Tubular Acidosis | Neutropenia | Large Granular Lymphocytic Leukemia | Fukuyama Congenital Muscular Dystrophy | Fibrodysplasia Ossificans Progressiva | Tyrosinemia Type 1 | Leukocyte Adhesion Deficiency Type 1 | IgA Nephropathy | Guillain-Barre Syndrome | Walker-Warburg Syndrome | Stroke, Ischemic | Peeling Skin Syndrome Type B | Spondylosis | Supravalvular Aortic Stenosis | Distal Myopathy 2 | Tatton-Brown-Rahman Syndrome | Hyperphenylalaninemia | Blau Syndrome | Carcinoma In Situ | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Gyrate Atrophy Of The Choroid And Retina | Vitamin A Deficiency | Adenylosuccinate Lyase Deficiency | Rheumatoid Arthritis | Otosclerosis | Trimethylaminuria | Cantu Syndrome | Hereditary Hemorrhagic Telangiectasia | Hypocalcemia | Spitz Nevus | Malnutrition | Maternally Inherited Diabetes And Deafness | Schizencephaly | Raine Syndrome | Argininosuccinic Aciduria | Arthritis, Psoriatic | Ectodermal Dysplasia | Hartnup Disease | Medulloblastoma | Cerebrovascular Disorders | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Vertigo | Proteus Syndrome | Congenital Nephrotic Syndrome | Vici Syndrome | Spinocerebellar Ataxia Type 21 | Parapsoriasis | Meningioma | Epidermolytic Hyperkeratosis | Hairy Cell Leukemia | Paracoccidioidomycosis | Epilepsy Of Infancy With Migrating Focal Seizures | Woodhouse-Sakati Syndrome | Niemann-Pick Disease, Type A | Cluster Headache | Ophthalmia, Sympathetic | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Larsen Syndrome | Sotos Syndrome | Muckle-Wells Syndrome | Spina Bifida | Urolithiasis | Dyskeratosis Congenita | Primary Hyperoxaluria Type 3 | Preaxial Polydactyly | Hypotonia-cystinuria Syndrome | Nager Acrofacial Dysostosis | Oculopharyngeal Muscular Dystrophy | Wieacker-Wolff Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Mucolipidosis Type IV | Anovulation | Pheochromocytoma | Craniometaphyseal Dysplasia | Isovaleric Acidemia | Pleomorphic Xanthoastrocytoma | Ocular Surface Squamous Neoplasia | Sick Sinus Syndrome | Urticaria | Congenital Ichthyosiform Erythroderma | 3-M Syndrome | Tumoral Calcinosis | Takotsubo Cardiomyopathy | Globozoospermia | Pilomatrix Carcinoma | Plasma Cell Leukemia | Urofacial Syndrome | Chromosome 8q21.11 Deletion Syndrome | Paget's Disease Of The Breast | Birt-Hogg-Dube Syndrome | Vitiligo | Aceruloplasminemia | Waardenburg Syndrome Type 2 | Pitt-Hopkins Syndrome | Lymphoma Lymphoblastic | Facioscapulohumeral Muscular Dystrophy | Hyperlipidemia Type V | Pure Red Cell Aplasia | Hypotrichosis Simplex | X-linked Sideroblastic Anemia | Myhre Syndrome | Benign Familial Infantile Seizures | Ichthyosis Bullosa Of Siemens | Pyruvate Decarboxylase Deficiency | Oral Lichen Planus | Rash | Hypertension, Pulmonary | Hypermethioninemia | ICF Syndrome | Harlequin Ichthyosis