Carcinoid Tumor

About the Disease
Carcinoid Syndrome, also known as carcinoid tumor, is related to carcinoid tumors, intestinal and appendix carcinoid tumor. An important gene associated with Carcinoid Syndrome is SDHD (Succinate Dehydrogenase Complex Subunit D), and among its related pathways/superpathways are Class A/1 (Rhodopsin-like receptors) and Signal Transduction. The drugs Pasireotide and Cyproheptadine have been mentioned in the context of this disorder. Affiliated tissues include heart, lung and small intestine, and related phenotypes are night sweats and small intestine carcinoid

Common Targets
NCOR1 | Vascular endothelial growth factors (VEGF) (nonspecified subtype) | MLH1 | G6774 | G3569 | SSTR2 | CIC | HIF1A | MAP3K2 | Protein Kinase B (PKB/Akt) (nonspecified subtype) | FKBP1A | Somatostatin receptor (nonspecified subtype) | G842 | RUNX3 | GH1 | CACNA1G | SSTR3 | SDHB | FGFR3 | SLC6A2 | ZFHX4 | G1029 | PDGFRB | APBA2 | Tyrosine Kinase (nonspecified subtype) | PTCH1 | G2475 | G999 | MEN1 | FLT4 | KMT2A | FLT1 | G836 | SST | FGFR1 | SDHD | SSTR5 | SDHA | APBA1 | SSTR1 | PDGFRA | TOP2A | G5243 | VHL | MGMT | RASSF2 | IGF2 | KDR | IPMK

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

Other Diseases

Encephalitis, Tick-borne | Arthritis, Reactive | Erdheim-Chester Disease | Mucormycosis | Viral Meningitis | Corneal Dystrophies, Hereditary | Cancer, Lung | Succinic Semialdehyde Dehydrogenase Deficiency | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Chudley-McCullough Syndrome | Alstrom Syndrome | Rotor Syndrome | Coma | Sick Sinus Syndrome | Oligospermia | Cantu Syndrome | Leukemia | Cerebral Amyloid Angiopathy | Heavy Chain Disease | Cancer, Breast | Membranous Nephropathy | Parkinson's Disease | Vasculitis | Cellulitis | Congenital Heart Defects | Pouchitis | Infantile Nephropathic Cystinosis | Acral Lentiginous Melanoma | Hyperbilirubinemia, Neonatal | Subcortical Band Heterotopia | Spinocerebellar Ataxia Type 8 | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Cystitis, Interstitial | B-cell Chronic Lymphocytic Leukemia | Hereditary Sensory Neuropathy Type 1 | Macrodactyly | Proctitis | Schuurs-Hoeijmakers Syndrome | Proopiomelanocortin Deficiency | Dystonia | Charcot-Marie-Tooth Disease, Type 6 | IgA Nephropathy | Multiple Sclerosis | Wolman Disease | Hyperthermia, Malignant | 3-methylglutaconic Aciduria Type IV | Branchiootorenal Syndrome | Preaxial Polydactyly | Multiple Myeloma | Vitamin K Deficiency | Crimean-Congo Hemorrhagic Fever | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Proteasome-associated Autoinflammatory Syndrome 2 | Myeloid Leukemia | Thrombocythemia, Essential | Castleman Disease | Hyperekplexia | Milk Allergy | Juvenile Polyposis | Dystonia-parkinsonism, X-linked | Familial Partial Lipodystrophy | Hodgkin Lymphoma | Martsolf Syndrome | Microcephaly | Epidermolytic Ichthyosis, Annular | Diabetic Nephropathy | Diabetic Macular Edema | Mitochondrial Encephalomyopathy | Hemimegalencephaly | Glutaric Aciduria Type 3 | Amblyopia | Ghosal Syndrome | Lymphoma Lymphoblastic | Hyperferritinemia-cataract Syndrome | Feingold Syndrome | Osteosclerosis | Craniometaphyseal Dysplasia | Glycogen Storage Disease Type 5 | Angelman Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Chromosome 17q21.31 Deletion Syndrome | Klinefelter Syndrome | Brooke-Spiegler Syndrome | Bursitis | Esophageal Motility Disorders | Cutaneous Mastocytosis | Kabuki Syndrome | Skin Papilloma | Ocular Surface Squamous Neoplasia | Aspartylglycosaminuria | Lipoma | Hemangioblastoma | Coronary Artery Disease | Cornelia De Lange Syndrome | Hemorrhagic Disorders | Vertebrobasilar Insufficiency | Congenital Mirror Movements | Familial Exudative Vitreoretinopathy | Hemolytic Anemia | Syndactyly | Delirium | Intestinal Obstruction | CDKL5 Deficiency Disorder | Glioblastoma | Nemaline Myopathy 10 | Absence Epilepsy | Lipid Storage Myopathy | Renal Hypomagnesemia 3 | Hereditary Pyropoikilocytosis | Sarcoma | Ileitis | Tinea | Hartsfield Syndrome | Silicosis | Myoclonus | Greig Cephalopolysyndactyly Syndrome | Neuropathy | Pompe Disease | Rickets | Focal Facial Dermal Dysplasia | Familial Hemiplegic Migraine | Basal Ganglia Disease | Myelomeningocele | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | HANAC Syndrome | Lymphangioma | Borderline Personality Disorder | Frank-ter Haar Syndrome | Porphyria | Autosomal Recessive Spastic Paraplegia Type 54 | Aldosteronism | Cirrhosis | Desmosterolosis | Myasthenia Gravis | Metachromatic Leukodystrophy | Hermansky-Pudlak Syndrome | Hamartoma | Amyotrophic Lateral Sclerosis, Juvenile | Essential Fructosuria | PASLI Disease | Glomerulonephritis | Congenital Torticollis | Peripheral Neuropathy | Wagner Disease | Hernia, Inguinal | Spinocerebellar Ataxia Type 5 | Pseudoachondroplasia | Acute Tubular Necrosis | Sitosterolemia | Generalized Epilepsy And Paroxysmal Dyskinesia | Glutaric Aciduria Type 2 | Pearson Syndrome | WAGR Syndrome | Bardet-Biedl Syndrome | Leukoplakia, Oral | Oculopharyngeal Muscular Dystrophy | Thyroid Dyshormonogenesis | Chronic Myeloid Leukemia | Turner's Syndrome | Bicuspid Aortic Valve | Beare-Stevenson Syndrome | Tricho-hepato-enteric Syndrome | Chorioretinitis | Pseudohermaphroditism | Influenza | Histiocytic Sarcoma | Alopecia | Arthritis | Dysmorphophobia | Chronic Beryllium Disease | Polycystic Ovary Syndrome | Chloridorrhea, Congenital | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Scleroderma | Intestinal Tuberculosis | Sclerocornea | Hartnup Disease | Trichomegaly | Familial Dysautonomia | Hereditary Hemorrhagic Telangiectasia Type 2 | Stroke, Ischemic | Polymyositis | Pure Autonomic Failure | Hyperandrogenemia | Stuve-Wiedemann Syndrome | Polyomavirus Nephropathy | Optic Neuropathy, Anterior Ischemic | Charcot-Marie-Tooth Disease, Type 2A | Cystinosis | Pancreatitis | Primrose Syndrome | Spasticity | Carpenter Syndrome | Malignant Fibrous Histiocytoma | Amish Infantile Epilepsy Syndrome | Sleep Disorder | Nanophthalmos | Retinal Diseases | Waardenburg Syndrome Type 2A | CHOPS Syndrome | Spinocerebellar Ataxia Type 17 | Hyperinsulinism-hyperammonemia Syndrome | Presbycusis | Diabetes Insipidus, Neurogenic | Hyperprolactinemia | Fuchs Dystrophy | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Asthma | Transient Bullous Dermolysis Of The Newborn | Stromal Corneal Dystrophy | Neurotoxicity | Subacute Sclerosing Panencephalitis | Acromicric Dysplasia | Multiple Sclerosis, Secondary Progressive | Motion Sickness | Restless Legs Syndrome | Blepharo-cheilo-odontic Syndrome | Congenital Hereditary Endothelial Dystrophy Type II | Asthma, Exercise-induced | Spinocerebellar Ataxia Type 15 | Combined Pituitary Hormone Deficiency | Congenital Myopathy | Congenital Myasthenic Syndrome | Pemphigus | Camptocormia | Myhre Syndrome | Alagille Syndrome | Focal Cortical Dysplasia Type 2 | Combined Malonic And Methylmalonic Acidemia | Tremor | Peeling Skin Syndrome, Acral Type | Hepatoblastoma | Schnyder Crystalline Corneal Dystrophy | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Alopecia Areata | Spinocerebellar Ataxia Type 40 | Sialidosis | Micro Syndrome | Allergic Contact Dermatitis | Partington Syndrome | Meconium Ileus | Anencephaly | Anorchia | Specific Granule Deficiency | Phenylketonuria | Mast Cell Leukemia | Abetalipoproteinemia | Plasma Cell Dyscrasia | Giant Cell Arteritis | Trichuriasis | Chondrodysplasia Punctata 2, X-linked Dominant | Acrodermatitis | Spinal Muscular Atrophy Type 2 | Blepharospasm | Eosinophilic Asthma | Carcinoid Tumor | Oral Lichen Planus | Leiomyosarcoma | Myasthenia | Menkes Disease | Hepatitis C, Chronic | Bruck Syndrome | Hypercholesterolemia, Familial | Glomerulonephritis, Membranoproliferative | Purpura, Thrombotic Thrombocytopenic | Blepharoconjunctivitis | Neuroectodermal Tumors, Primitive | Alazami Syndrome | Azoospermia | Barakat Syndrome | Transcobalamin Deficiency | Pancytopenia | Mitochondrial DNA Depletion Syndrome 13 | Myoclonus-dystonia Syndrome | Paracoccidioidomycosis | Retinoschisis | Epilepsy | Alzheimer Disease, Late Onset | Prolidase Deficiency | Spondylolisthesis | Myosin Storage Myopathy | Dent Disease | Graves Disease | Angiodysplasia | Spinocerebellar Ataxia Type 2 | Zygomycosis | Spinal Muscular Atrophy Type 3 | Spinocerebellar Ataxia Type 6 | Perry Syndrome | Infantile Refsum Disease | Colitis, Microscopic | Blue Rubber Bleb Nevus Syndrome | Cerebellar Ataxia, Cayman Type | Meier-Gorlin Syndrome | Corneal Dystrophy | Pelizaeus-Merzbacher Disease | Schistosomiasis | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Esophageal Carcinoma | Tietze Syndrome | Acute Leukemia | Cardiofaciocutaneous Syndrome | Early Infantile Epileptic Encephalopathy 1 | Anovulation | Lafora Disease | Thalassemia | Klippel-Feil Syndrome | Hyperuricemic Nephropathy, Familial Juvenile | Coffin-Lowry Syndrome | Gardner Syndrome | Antithrombin III Deficiency | Spinal Muscular Atrophy | Conjunctivitis, Allergic | Thyroid Hormone Resistance | Granular Corneal Dystrophy Type 1 | Sialoadenitis | Actinomycetoma | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Pulmonary Veno-occlusive Disease | Jalili Syndrome | Intracranial Hypertension | Thrombosis | Erysipelas | Myofibrillar Myopathy | Microphthalmia, Syndromic 7 | Avian Influenza | Apparent Mineralocorticoid Excess Syndrome | Heart Block | Thalassemia, Beta | Congenital Disorders Of Glycosylation Type II | HUPRA Syndrome | Inflammatory Joint Disease | Glycogen Storage Disease Type 1b | Lactose Intolerance | Sertoli Cell-only Syndrome | Meningococcal Infections | Chronic Myelomonocytic Leukemia | Pituitary Stalk Interruption Syndrome | Pachyonychia Congenita | Familial Mediterranean Fever | Protein C Deficiency | Hereditary Sensory And Autonomic Neuropathy | Urolithiasis | Connective Tissue Disorders | Congenital Hemolytic Anemia | Macular Degeneration | Cholangiocarcinoma | Plasmacytoma | Familial Hyperaldosteronism | Alopecia Totalis | Borjeson-Forssman-Lehmann Syndrome | Ureteropelvic Junction Obstruction | Intellectual Disability, Autosomal Dominant 5 | Pituitary Disorders | Ornithine Transcarbamylase Deficiency | Osteopathia Striata With Cranial Sclerosis | Osteogenesis Imperfecta Type VI | Charcot-Marie-Tooth Disease Type 2D | Beta-Propeller Protein-associated Neurodegeneration | Cranioectodermal Dysplasia | Pulverulent Zonular Cataract | Familial Thoracic Aortic Aneurysm | Hypertension | Acute Lymphocytic Leukemia | Hypersensitivity Pneumonitis | Primary Lateral Sclerosis | Gangliosidosis | Premenstrual Syndrome | Spinal And Bulbar Muscular Atrophy | Cannabis Abuse | Waldenstrom Macroglobulinemia | Fibromuscular Dysplasia | Diamond-Blackfan Anemia | Endometrial Hyperplasia | Colon Adenoma | Arthropathy | Platelet Disorders | Meningioma | Retinopathy Of Prematurity | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Pneumonia, Bacterial | Ganglioneuroma | Sezary Syndrome | Emery-Dreifuss Muscular Dystrophy | Joubert Syndrome 2 | H Syndrome | Polycystic Kidney, Autosomal Dominant | Methylmalonic Acidemia | Charcot-Marie-Tooth Disease, Type 1A | Aplasia Cutis Congenita | Leber Hereditary Optic Neuropathy | Osteogenesis Imperfecta Type IV | Frontotemporal Dementia | Pneumothorax | Sarcomatoid Carcinoma Of The Lung | Creutzfeldt-Jakob Disease | Primary Hyperoxaluria Type 3 | Graft-versus-host Disease | Bartter Syndrome | Diabetes