Pneumothorax

About the Disease
Pneumothorax, also known as pleural air leak nos, is related to pneumothorax, primary spontaneous and pleural disease, and has symptoms including dyspnea and hemoptysis. An important gene associated with Pneumothorax is FLCN (Folliculin), and among its related pathways/superpathways are ERK Signaling and Signal Transduction. The drugs Lidocaine and Propofol have been mentioned in the context of this disorder. Affiliated tissues include lung, heart and lymph node, and related phenotypes are no effect and no effect

Common Targets
G4318 | LOC439933 | LINC02147 | MMP12 | TACC1 | DNAH3 | CDKAL1 | ADARB2 | LINC01091 | ZNF407 | PDE1C | LOC105375639 | IMMP2L | PRKD1 | IQGAP2 | ARHGAP24 | TNFSF10 | LOC105371072 | LUZP2 | SYN3 | TNNI3K | FRMD4A | CSMD1 | PARVG | DISC1FP1 | TMEM132D | DLG2 | AKAP2 | ZFAT | CFTR | LOC105376193 | CNTNAP2 | SLC6A1 | NPSR1-AS1 | FUT2 | MMP1 | TLL2 | LINC02742 | NPAS3 | CPED1 | CCDC162P | CDH13 | CCK | MAGI2 | G142 | EPHB1 | MACROD2 | LOC105370311 | SH3GL3 | PTPRD | LEKR1 | FLCN | ARID1B | RBFOX1

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

Other Diseases

Medium-chain Acyl-CoA Dehydrogenase Deficiency | Scoliosis | Allan-Herndon-Dudley Syndrome | Kleine-Levin Syndrome | Diabetes Gestational | Connective Tissue Disorders | Eczema | Lymphoma, Follicular | Osteogenesis Imperfecta | Astigmatism | Hyperbilirubinemia | Pseudohypoparathyroidism Type 1C | Omenn Syndrome | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Shprintzen-Goldberg Syndrome | Methylmalonic Acidemia | Peyronie's Disease | Encephalopathy, Ethylmalonic | Thrombocythemia, Essential | Spinocerebellar Ataxia Type 31 | Trichotillomania | Microcephaly, Seizures, And Developmental Delay | Bardet-Biedl Syndrome | Polycystic Kidney, Autosomal Dominant | Lipodystrophy | Oculocutaneous Albinism Type 4 | Follicular Dendritic Cell Sarcoma | Familial Male-limited Precocious Puberty | Thyroid Dyshormonogenesis | Kallmann Syndrome | Graves Disease | Congenital Bile Acid Synthesis Defect | Tuberculosis | Paraplegia | Cryoglobulinemia | Thalassemia, Beta | Familial Hyperaldosteronism | Carney-Stratakis Syndrome | Colon Adenoma | Pontocerebellar Hypoplasia | Trimethylaminuria | Autosomal Recessive Congenital Ichthyosis | DOCK8 Immunodeficiency Syndrome | Pulmonary Sclerosing Hemangioma | Usher Syndrome Type III | Cat Eye Syndrome | Cutaneous Lupus Erythematosus | Thrombasthenia | Retinitis Pigmentosa 3 | Urolithiasis | Endometrial Hyperplasia | Alazami Syndrome | HUPRA Syndrome | Obsessive-compulsive Disorder | Hyperhomocysteinemia | Lymphangioma | Hypercalciuria | Nance-Horan Syndrome | Osteogenesis Imperfecta Type IV | Thrombotic Microangiopathy | Myoclonus-dystonia Syndrome | Cerebral Cavernous Malformations | Cataplexy | Cocaine-Related Disorders | Choriocarcinoma | Acute Myeloid Leukemia | Hepatitis, Chronic | Brenner Tumor | Van Der Knaap Disease | Skin Papilloma | Relapsing Polychondritis | Osteonecrosis | Dyggve-Melchior-Clausen Disease | Generalized Epilepsy With Febrile Seizures Plus | Carcinoma, Small Cell | Schistosomiasis Mansoni | Conjunctivitis, Allergic | Becker Muscular Dystrophy | Duane Retraction Syndrome | Neutrophilia | Glycogen Storage Disease Type 6 | Albinism | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Poikiloderma With Neutropenia | Corneal Dystrophy And Perceptive Deafness | Cutaneous T-cell Lymphoma | Mohr-Tranebjaerg Syndrome | Myofibromatosis | Microtia | Tic Disorder | Renal Tubular Acidosis | Angelman Syndrome | Takotsubo Cardiomyopathy | Schizotypal Personality Disorder | Glycogen Storage Disease Type 5 | Carney Triad | Lactose Intolerance | Hypercholesterolemia, Familial | Mabry Syndrome | Focal Segmental Glomerulosclerosis | Joubert Syndrome 2 | Craniolenticulosutural Dysplasia | Melanoma, Malignant | Roberts Syndrome | Cancer, Skin | Tremor | Peritonitis | Antithrombin III Deficiency | Pearson Syndrome | Oculodentodigital Dysplasia | Paraganglioma, Carotid Body | Muir-Torre Syndrome | Rosacea | Epilepsy | CREST Syndrome | Intestinal Hypomagnesemia 1 | Leishmaniasis, Cutaneous | Polycystic Liver | Cardiomyopathy, Peripartum | Dermatomyositis | Pompe Disease | Familial Digital Arthropathy-brachydactyly | Molybdenum Cofactor Deficiency | Glycogen Storage Disease Type 9 | Metatropic Dysplasia | Charcot-Marie-Tooth Disease Type 4D | Cyst | Leukoplakia, Oral | Intermittent Claudication | Autism Spectrum Disorders | Chondroma | Spinocerebellar Ataxia Type 6 | Leri Pleonosteosis | Retinal Dystrophy, Early-onset Severe | Charcot-Marie-Tooth Disease | Erythromelalgia | Fraser Syndrome | Congenital Nephrotic Syndrome | Avian Influenza | Auriculocondylar Syndrome | Monilethrix | Multiple Sclerosis, Chronic Progressive | Nephropathy | Spondyloepimetaphyseal Dysplasia With Joint Laxity, Type 3 | Hashimoto Thyroiditis | Hyperinsulinemia | Dysthymia | Anorchia | Palmoplantar Keratoderma | Myelitis | Gnathodiaphyseal Dysplasia | Stroke, Ischemic | Trichorhinophalangeal Syndrome | Growth Hormone Excess | Neuromyelitis Optica | Hypertelorism | Hemolytic Anemia | C3 Glomerulonephritis | Chronic Leukemia | Nephronophthisis | Perry Syndrome | Heart Failure | Acromesomelic Dysplasia | Microphthalmia, Syndromic 7 | Tatton-Brown-Rahman Syndrome | Gastrointestinal Disorders | Cholera | Eiken Syndrome | Sponastrime Dysplasia | Osteogenesis Imperfecta Type I | Brugada Syndrome 1 | Premature Ejaculation | Hydrocephalus, Normal Pressure | Persistent Hyperplastic Primary Vitreous | Chorea | Cherubism | Membranous Nephropathy | Hyperandrogenemia | Diverticulitis | Peters-plus Syndrome | Hepatitis E | Stomatitis | Nicolaides-Baraitser Syndrome | Encephalopathy | Influenza | Retinal Vasculitis | Osteomalacia | Norrie Disease | Cystinosis | Oguchi Disease-2 | Dermatitis | DNA Ligase IV Deficiency | Greig Cephalopolysyndactyly Syndrome | Holt-Oram Syndrome | Hydrocephalus | COACH Syndrome | Congenital Sodium Diarrhea | Ectrodactyly | Hereditary Neuropathy With Liability To Pressure Palsies | Lung Diseases | Lichen Sclerosus | Multisystemic Smooth Muscle Dysfunction Syndrome | Angiosarcoma Of The Breast | Neurodevelopmental Disorders | Sclerosing Cholangitis | Farber Disease | Androgenic Alopecia | Niemann-Pick Disease | Epidermolysis Bullosa Simplex | Charcot-Marie-Tooth Disease Type 4 | Hypoplastic Left Heart Syndrome | Superficial Spreading Melanoma | Esotropia | Lattice Corneal Dystrophy Type 1 | Gestational Trophoblastic Disease | Anosmia, Congenital | Diabetes Type 2 | Eating Disorder | Angiodysplasia | Papillorenal Syndrome | Burn-McKeown Syndrome | Heroin Dependence | Postaxial Polydactyly | Nephrotic Syndrome Type 1 | Lipoma | Knobloch Syndrome | Spondylo-ocular Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Neural Tube Defect | Blepharophimosis Syndrome | Corneal Ulcer | Spondyloepiphyseal Dysplasia Tarda, X-linked | Ocular Hypertension | Cold Agglutinin Disease | Common Variable Immunodeficiency | Bloom Syndrome | Coronary Artery Disease | Microphthalmia | Intermittent Explosive Disorder | Meleda Disease | Branchiootorenal Syndrome | Gynecomastia | Sickle Cell Disease | Frontometaphyseal Dysplasia | Spinal Muscular Atrophy Type 2 | Fascioliasis | Primary Hyperoxaluria Type 1 | Epidermolytic Ichthyosis, Annular | Autoimmune Polyendocrinopathy Syndrome Type I | Inborn Errors Of Metabolism | REM Sleep Behavior Disorder | Early Infantile Epileptic Encephalopathy | Epithelial-myoepithelial Carcinoma | Delirium | Asphyxia Neonatorum | Asplenia | Trichuriasis | Oral Lichen Planus | Sarcoidosis, Pulmonary | Hepatitis, Autoimmune | Spondylometaphyseal Dysplasia | Erythematotelangiectatic Rosacea | Hepatic Veno-occlusive Disease | Lipid Metabolism Disorders | Cerebrotendinous Xanthomatosis | Otitis Externa | Woodhouse-Sakati Syndrome | Megalencephaly | Multiple Hamartoma Syndrome | Infantile Nephropathic Cystinosis | Glycogen Storage Disease Type 4 | Epidermodysplasia Verruciformis | Pigment Dispersion Syndrome | Spastic Paraplegia Type 7 | Meniere's Disease | Huntington's Disease | Restrictive Dermopathy | Gaucher Disease | 3C Syndrome | Macrophage Activation Syndrome | Phosphoglycerate Dehydrogenase Deficiency | Pain | Pseudoachondroplasia | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Robinow Syndrome | Non-small Cell Lung Cancer | Trismus-pseudocamptodactyly Syndrome | Disseminated Intravascular Coagulation | Hyper IgE Syndrome | Hypopigmentation | Chromosome 8q21.11 Deletion Syndrome | VACTERL/VATER Association | Blastomycosis | Blood Protein Disorders | Spermatocele | Lymphoma, Mantle Cell | Spinocerebellar Ataxia Type 1 | Jaundice, Obstructive | Primary Pigmented Nodular Adrenocortical Disease | Progressive Familial Intrahepatic Cholestasis Type 3 | Pituitary Stalk Interruption Syndrome | Parkinson Disease 6, Autosomal Recessive Early-onset | Cystitis, Interstitial | D-2-Hydroxyglutaric Aciduria | Primary Familial Brain Calcification | Pemphigus Foliaceus | Non-proliferative Diabetic Retinopathy | Familial Retinal Arterial Macroaneurysm | Autonomic Nervous System Disorders | Nemaline Myopathy 10 | Porokeratosis | Viral Meningitis | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | L-2-Hydroxyglutaric Aciduria | Keratoacanthoma | Language Disorders | Hemimegalencephaly | Osteosclerosis | Guanidinoacetate Methyltransferase Deficiency | Chromosome 9q34.3 Deletion Syndrome | HIBCH Deficiency | Shock, Cardiogenic | Vaginitis | Hennekam Lymphangiectasia-lymphedema Syndrome | Coloboma | Patent Ductus Arteriosus | IMAGe Syndrome | Familial Dysautonomia | Diabetes Insipidus | Actinomycetoma | Erdheim-Chester Disease | Bernard-Soulier Syndrome | Retinopathy, Diabetic | Venous Insufficiency | Restless Legs Syndrome | Congenital Dyserythropoietic Anemia Type 1 | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Optic Neuritis | Leiomyoma | Hemorrhage | Pseudomyxoma Peritonei | Anti-NMDA Receptor Encephalitis | Cutis Laxa | Proctitis | Plasma Cell Leukemia | Hypersensitivity Pneumonitis | Diabetic Macular Edema | CDKL5 Deficiency Disorder | Renal Hypouricemia | Fetal And Neonatal Alloimmune Thrombocytopenia | Autoimmune Polyendocrine Syndrome | Tonsillitis | Familial Pheochromocytoma-paraganglioma | Crigler-Najjar Syndrome | Hyperthyroidism | Corneal Dystrophy | Tyrosine Hydroxylase Deficiency | Medulloblastoma | Pyoderma Gangrenosum | Pfeiffer Syndrome | Familial Episodic Pain Syndrome | Pleurisy | Platelet Disorders | Sialidosis | Spinocerebellar Ataxia Type 42 | Hereditary Inclusion Body Myopathy | Hypotrichosis | Paroxysmal Nocturnal Hemoglobinuria | Primary Sclerosing Cholangitis | Acute Leukemia | Scleritis | Inflammatory Myopathy | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Glycogen Storage Disease | Pyelonephritis | Glaucoma | Usher Syndrome | Apparent Mineralocorticoid Excess Syndrome | Myelofibrosis | Early Infantile Epileptic Encephalopathy 28 | Carpenter Syndrome | Rhabdomyosarcoma | Optic Neuropathy | Infectious Diarrhea | Galactosemia | Seborrheic Dermatitis | Systemic Lupus Erythematosus | Polyomavirus Nephropathy | Oculocutaneous Albinism Type 2 | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Long QT Syndrome Type 2 | Zollinger-Ellison Syndrome | Spinocerebellar Ataxia Type 38 | Currarino Syndrome | Neurodegeneration With Brain Iron Accumulation | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Sengers Syndrome | Veno-occlusive Disease | Melanoma | Alkaptonuria