Small Cell Carcinoma

About the Disease
Lung Oat Cell Carcinoma, also known as carcinoma, small cell, is related to esophagus small cell carcinoma and prostate small cell carcinoma. An important gene associated with Lung Oat Cell Carcinoma is RB1 (RB Transcriptional Corepressor 1), and among its related pathways/superpathways are Disease and Cytokine Signaling in Immune system. The drugs BCG vaccine and Atezolizumab have been mentioned in the context of this disorder. Affiliated tissues include lung, cervix and prostate, and related phenotypes are nervous system and neoplasm

Common Targets
TOP1 | SMARCA4 | CLPTM1L

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Other Diseases

Chronic Kidney Disease | DICER1 Syndrome | Lymphomatoid Granulomatosis | Dentinogenesis Imperfecta | Carney Triad | Tetraplegia | Barrett Esophagus | Alopecia Totalis | Spinal Muscular Atrophy Type 2 | Achondrogenesis | Esotropia | Lathosterolosis | Tricho-hepato-enteric Syndrome | Hypervalinemia | Familial Advanced Sleep Phase Syndrome | Antiphospholipid Syndrome | Mucolipidosis Type II | Hashimoto Thyroiditis | Familial Dysautonomia | Glycogen Storage Disease Type 0, Muscle | Pneumonia, Mycoplasma | Familial Mediterranean Fever | Usher Syndrome | Hereditary Multiple Exostoses | AIDS Dementia Complex | Asplenia | Scleroderma, Diffuse | Sarcomatoid Carcinoma Of The Lung | Spinocerebellar Ataxia Type 42 | Perivascular Epithelioid Cell Tumor | Hyperprolactinemia | Retinal Coloboma | Zygomycosis | Hereditary Mixed Polyposis Syndrome | Neuroblastoma | Pseudohypoaldosteronism | Porphyria | Olmsted Syndrome | Branchiootorenal Syndrome | Nance-Horan Syndrome | Hypothalamic Obesity | Retinitis | Pycnodysostosis | Spinocerebellar Ataxia Type 16 | Leber Hereditary Optic Neuropathy | Mountain Sickness | Trichotillomania | Myhre Syndrome | Spondyloepiphyseal Dysplasia Tarda, X-linked | Optic Neuritis | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Acne | Presbyopia | Cyst | Kidney Stones | Charcot-Marie-Tooth Disease Type 4E | Charcot-Marie-Tooth Disease Type 2T | Renal Oncocytoma | Walker-Warburg Syndrome | Hydrops Fetalis | Mandibuloacral Dysplasia With Type A Lipodystrophy | Lennox-Gastaut Syndrome | Argininosuccinic Aciduria | Crigler-Najjar Syndrome | Polyomavirus Nephropathy | Dyslexia | Hemoglobinopathies | Varices | Acute Generalized Exanthematous Pustulosis | Schizoaffective Disorder | Onchocerciasis | Actinomycetoma | Campomelic Dysplasia | Lattice Corneal Dystrophy Type 1 | Hyperferritinemia-cataract Syndrome | Agranulocytosis | Roberts Syndrome | Okihiro Syndrome | Hernia, Inguinal | Chronic Granulomatous Disease, X-linked | Delirium | Congenital Hemolytic Anemia | Anorectal Fistula | Usher Syndrome Type III | Arthritis, Reactive | Kabuki Syndrome | Atrioventricular Septal Defect | Autoimmune Polyendocrinopathy Syndrome Type I | Renal Hypomagnesemia 3 | Dysplastic Nevus | Neuromyotonia | Meniere's Disease | Muscular Dystrophy | 3-methylglutaconic Aciduria | Keratoacanthoma | McCune-Albright Syndrome | Sarcoidosis, Pulmonary | Multiple Epiphyseal Dysplasia | Histiocytic Sarcoma | Inflammatory Bowel Disease | Raine Syndrome | Cutaneous Angiosarcoma | Tibial Muscular Dystrophy | Oligospermia | Agammaglobulinemia | Congenital Stationary Night Blindness | Netherton Syndrome | Heterotopic Ossification | Pachyonychia Congenita | Motion Sickness | Distal Myopathy 2 | Sarcoma, Endometrial Stromal | Desbuquois Syndrome | Pemphigus Vulgaris | Spinocerebellar Ataxia Type 1 | Tonsillitis | Gyrate Atrophy Of The Choroid And Retina | Panniculitis | Cataract | Holoprosencephaly | Hemophagocytic Lymphohistiocytosis | Alcoholism | Goldenhar Syndrome | Giant Cell Glioblastoma | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Vaginitis | Hemochromatosis | LEOPARD Syndrome | Hypersomnia | Cholecystitis | Multiple Sclerosis, Relapsing-remitting | Localized Scleroderma | Thrombocytopenia | Stargardt Disease | Micro Syndrome | Endocarditis | Glomerulonephritis | Vitreoretinal Degeneration, Snowflake Type | Dermatomyositis | Cystitis | Blepharophimosis Syndrome | H Syndrome | Atelosteogenesis Type 1 | Stevens-Johnson Syndrome | Leigh Syndrome | Retinitis Pigmentosa 3 | Filariasis | Delayed Sleep Phase Syndrome | Osteogenesis Imperfecta Type I | Oguchi Disease-2 | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Norrie Disease | Muckle-Wells Syndrome | Panuveitis | MIRAGE Syndrome | Lichen Sclerosus | Phenylketonuria | Osteogenesis Imperfecta Type IV | Costello Syndrome | Periodic Limb Movement Disorder | Tyrosinemia Type 1 | Acute Lung Injury | Common Cold | Early Infantile Epileptic Encephalopathy 1 | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Split Hand-foot Malformation | Oculocutaneous Albinism | Sleep Apnea, Obstructive | Liebenberg Syndrome | Hypogammaglobulinemia | ACTH-independent Macronodular Adrenal Hyperplasia | Diffuse Intrinsic Pontine Glioma | Tuberculous Meningitis | Sarcoidosis | Focal Facial Dermal Dysplasia | Growth Hormone Excess | Myelofibrosis | Blue Nevus | Sporadic Hemiplegic Migraine | Papulopustular Rosacea | Fraser Syndrome | Polycythemia Vera | Niemann-Pick Disease, Type C | Hemangioma | Fibrosarcoma | Cerebrotendinous Xanthomatosis | Benign Familial Pemphigus | Skin Carcinoma | Chylothorax, Congenital | Miyoshi Myopathy | Spinocerebellar Ataxia Type 3 | HUPRA Syndrome | B-cell Chronic Lymphocytic Leukemia | Vogt-Koyanagi-Harada Syndrome | Reflex Epilepsy | Spondylocarpotarsal Synostosis Syndrome | Pneumococcal Meningitis | Menkes Disease | Anuria | Sialidosis Type I | Duane Retraction Syndrome | Spinocerebellar Ataxia Type 7 | Seizures-scoliosis-macrocephaly Syndrome | Tinea | Lymphoproliferative Disease, X-linked | Neuromuscular Disorders | Premature Ejaculation | Thrombophlebitis | Silver-Russell Syndrome | Prostatitis | Craniosynostosis | Nail-Patella Syndrome | Angioimmunoblastic T-cell Lymphoma | Knobloch Syndrome | Uterine Leiomyoma | Microphthalmia, Syndromic 7 | Sleep Disorder | Sclerosteosis | Pneumonia, Viral | Lassa Fever | Pierre Robin Syndrome | Pulmonary Alveolar Microlithiasis | Alazami Syndrome | Centronuclear Myopathy | Acquired Partial Lipodystrophy | Saul-Wilson Syndrome | Huntington's Disease | Pineoblastoma | POEMS Syndrome | Leri-Weill Dyschondrosteosis | Fascioliasis | Cancer, Prostate | Oligoastrocytoma | Carpenter Syndrome | Shprintzen-Goldberg Syndrome | Bronchitis, Chronic | Allergic Contact Dermatitis | Thrombasthenia | Hypertriglyceridemia | Metatropic Dysplasia | Peripheral Neuropathy | Carbohydrate Metabolism Disorders | Prune Belly Syndrome | Arthritis | Schistosomiasis Mansoni | Diabetes | Cartilage Disorders | Sick Sinus Syndrome | Mucormycosis | Astrocytoma | Arthropathy | Open-angle Glaucoma | Temtamy Preaxial Brachydactyly Syndrome | Blastomycosis | DNA Ligase IV Deficiency | Colitis, Collagenous | Waldenstrom Macroglobulinemia | Scapuloperoneal Spinal Muscular Atrophy | Subacute Sclerosing Panencephalitis | Neural Tube Defect | Mitochondrial Myopathy | Erythema Nodosum | HIBCH Deficiency | Haim-Munk Syndrome | Spinocerebellar Ataxia Type 15 | Lesch-Nyhan Syndrome | Dermatitis | Optic Neuropathy, Anterior Ischemic | Obsessive-compulsive Disorder | Heavy Chain Disease | Granular Corneal Dystrophy | Thrombotic Microangiopathy | Familial Hypobetalipoproteinemia | Martsolf Syndrome | Blomstrand Osteochondrodysplasia | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Epidermolysis Bullosa Dystrophica | Primary Ovarian Insufficiency | Nevus | Salla Disease | Duodenal Atresia | Multicentric Carpotarsal Osteolysis Syndrome | Cerebrovascular Disorders | Lipid Storage Diseases | Hypoalbuminemia | Majeed Syndrome | Congenital Stromal Corneal Dystrophy | Auriculocondylar Syndrome | Hypercalcemia | Cancer, Brain | Glucagonoma | ICF Syndrome | Multicystic Renal Dysplasia | Azoospermia | Neurofibroma | Eczema | Blastoma, Pleuropulmonary | Apert Syndrome | Tay-Sachs Disease | Parkinsonism | Myosin Storage Myopathy | Long QT Syndrome Type 2 | Renal Hypouricemia | Adrenomyeloneuropathy | Cockayne Syndrome | Osteochondroma | Craniofacial Dysostosis | Macular Corneal Dystrophy | Dengue Shock Syndrome | Juvenile Hyaline Fibromatosis | Iron Metabolism Disorders | Epithelial-myoepithelial Carcinoma | Cellulitis | Exotropia | Juvenile Myelomonocytic Leukemia | Restrictive Dermopathy | Raynaud Phenomenon | Chronic Thromboembolic Pulmonary Hypertension | Cone Dystrophy | Malonyl-CoA Decarboxylase Deficiency | Hypercholesterolemia, Familial | Pyruvate Decarboxylase Deficiency | Nephronophthisis | Down Syndrome | Atherosclerosis | Hypotrichosis Simplex | Usher Syndrome Type II | Inflammatory Linear Verrucous Epidermal Nevus | Paraplegia | Papillorenal Syndrome | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Leiomyoma | Primary Hyperoxaluria Type 1 | Eosinophilia | VACTERL Association | Occipital Neuralgia | Polycystic Kidney, Autosomal Dominant | Angioedema | Sjogren Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Progressive Encephalopathy-optic Atrophy Syndrome | Hemophilia | Joubert Syndrome | Plasmacytoma | Optic Nerve Diseases | C3 Glomerulopathy | Gastric Atrophy | Schwannomatosis | Pseudo-pseudohypoparathyroidism | Insulin Resistance | Familial Partial Lipodystrophy | Disseminated Superficial Actinic Porokeratosis | VACTERL/VATER Association | Pericarditis | Urolithiasis | Angelman Syndrome | Hereditary Neuropathy With Liability To Pressure Palsies | Esophageal Adenocarcinoma | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Goiter | Spinocerebellar Ataxia Type 38 | Kallmann Syndrome | Saethre-Chotzen Syndrome | Tic Disorder | Arrhythmogenic Right Ventricular Cardiomyopathy | Sandhoff Disease | Hyperinsulinemic Hypoglycemia | Orthostatic Intolerance | Hyperlipidemia, Familial Combined | Retinoschisis | Apraxia | Leri Pleonosteosis | Urofacial Syndrome | Incontinentia Pigmenti | Hyperthermia, Malignant | Woodhouse-Sakati Syndrome | Atopy | Aldosterone Synthase Deficiency | Fibrodysplasia Ossificans Progressiva | Meier-Gorlin Syndrome | Peritonitis | Schindler Disease | Corneal Ulcer | Mitochondrial Encephalomyopathy | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Leukoplakia, Oral | HELLP Syndrome | Pilomatrix Carcinoma | Thrombophilia | Primary Progressive Nonfluent Aphasia | Peutz-Jeghers Syndrome | Aspartylglycosaminuria | Inflammatory Myofibroblastic Tumor | Microphthalmia | Citrullinemia | Colorectal Adenoma | Neurofibromatosis-Noonan Syndrome | Congenital Nystagmus | 3-hydroxy-3-methylglutaric Aciduria | Choroiditis