Disease

Pulmonary Tuberculosis

About the Disease
Pulmonary Tuberculosis, also known as tuberculosis, pulmonary, is related to laryngeal tuberculosis and miliary tuberculosis, and has symptoms including fever, cough and difficulty in breathing. An important gene associated with Pulmonary Tuberculosis is IFNG (Interferon Gamma), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. The drugs Rifabutin and Calcium carbonate have been mentioned in the context of this disorder. Affiliated tissues include lungs, lung and liver, and related phenotypes are no effect and no effect

Common Targets
IL4 | TLR1 | INSL6 | MIR505 | DEUP1 | CUBN | CD40LG | POLD1 | IL10 | FCN2 | IL18 | IL23R | MIR149 | IL27RA | LINC00968 | CTR9 | CYP3A4 | IL6ST | G7124 | HAMP | JAK1 | CDH13 | IRF1 | IL23A | HLA-DQB1 | SOCS1 | G3576 | TLR8 | MADD | CYP7A1 | LYRM4 | G2335 | IL12B | SFTPA1 | CD1A | MRPS18B | MYD88 | JAK2 | IL6-AS1 | ANXA11 | PARP9 | NR1H2 | EBI3 | NOD1 | IL1B | TMED7-TICAM2 | G6774 | IFNGR1 | IL10RA | TOLLIP | G207 | DROSHA | TBX21 | GEMIN4 | NR1H3 | TICAM2 | G6352 | SDR16C6P | LOC105371082 | G3569 | Uncharacterized LOC105373806, transcript variant X1 | TNFAIP1 | WIPI2 | HLA-DQA1 | IL12RB1 | GBE1 | ATG16L1 | CSF1R | LACC1 | TIRAP | MAOA | TYK2 | NOD2 | FOXP1 | VTI1B | G7099 | MR1 | HLA-B | IFNGR2 | G6772 | DGCR8 | LOC105374224 | CTSZ | IL27 | SMURF1 | IL12RB2 | SP110 | CYP24A1 | MC3R | TMED7 | HLA-DRB1 | NPIPB8 | G2309 | TICAM2-AS1 | CYP2R1 | G3605 | SFTPA2 | MYBBP1A | DICER1 | NADSYN1 | LOC285626 | CD1D | MBL2 | HLA-A | CXCL12 | SFTPD | TCIRG1 | RXRA | Cytochrome P450 Enzymes (nonspecified subtype) | TLR2 | G5970 | STAT4 | TOX | VAMP8 | IFNAR1 | IL12A-AS1 | TGM6 | CYP27A1 | AGMO | G2069 | IL12A | TNXB | GC | PON1 | PTPN22 | TNFSF15 | RIC1 | UBXN2B | QPRT | LRP2 | LYN | IL2 | DEFB1 | TLR6 | G820 | SLC11A1 | MST1 | MIR6753 | IRAK1 | TLR9 | CTLA4 | VDR | CCL2 | AGO1 | XKR4 | CYP27B1 | NOS2 | MIF | P2RX7 | LTA4H | MIR196A2 | IFNG | LOC105379176 | MARCO | CCL3 | MIR499A

疾病靶点研报
Pulmonary Tuberculosis

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

Other Diseases

Myelofibrosis | Pseudoachondroplasia | Esophageal Adenocarcinoma | Hyperuricemia | Multiple System Atrophy | Juvenile Polyposis | Primary Erythromelalgia | Paracoccidioidomycosis | Early Infantile Epileptic Encephalopathy 28 | Anorchia | Jawad Syndrome | Subacute Sclerosing Panencephalitis | Neurogenic Bladder | Choroiditis | Binge Eating Disorder | Platelet Disorders | Seminoma | Osteomyelitis | Aplasia Cutis Congenita | Hypohidrotic Ectodermal Dysplasia, X-linked | Infertility | Fetal Akinesia Deformation Sequence | Leigh Syndrome | 3-hydroxyacyl-CoA Dehydrogenase Deficiency | Interstitial Lung Diseases | Gestational Trophoblastic Disease | Glaucoma | Peyronie's Disease | Kohlschutter-Tonz Syndrome | Sarcoma | Pompe Disease | Photosensitivity | Familial Mediterranean Fever | Gliosarcoma | Glomerulonephritis, Membranous | Reye Syndrome | Cerebellofaciodental Syndrome | GNE Myopathy | Cancer, Colon | Thanatophoric Dysplasia | Arteriovenous Malformations | Lymphomatoid Granulomatosis | Transient Bullous Dermolysis Of The Newborn | Chondromyxoid Fibroma | Dyggve-Melchior-Clausen Disease | Ornithine Transcarbamylase Deficiency | Alazami Syndrome | Endocarditis | Myosin Storage Myopathy | Plasma Cell Dyscrasia | Keratosis, Seborrheic | Mumps | 3-M Syndrome | Peripheral T-cell Lymphoma | Antisynthetase Syndrome | Myositis, Focal | Smith-Kingsmore Syndrome | Epithelial-myoepithelial Carcinoma | Retinal Dystrophy | Coronary Restenosis | Facioscapulohumeral Muscular Dystrophy Type 1 | Alpha-1 Antitrypsin Deficiency | Chylothorax, Congenital | Plasmacytoma | Cancer, Breast | Chondrodysplasia Punctata | Aneurysm, Thoracic Aortic | Cholera | Autosomal Recessive Bestrophinopathy | Guillain-Barre Syndrome | Pleural Tuberculosis | Hypersomnia | Reticular Dysgenesis | Ataxia-ocular Apraxia 2 | Lymphangioleiomyomatosis | Haim-Munk Syndrome | Bardet-Biedl Syndrome | Alopecia | Glaucomatocyclitic Crisis | Recurrent Respiratory Papillomatosis | Spinocerebellar Ataxia Type 23 | Osteonecrosis Of The Jaw | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Autonomic Nervous System Disorders | Gnathodiaphyseal Dysplasia | Parkinson Disease 6, Autosomal Recessive Early-onset | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Nail-Patella Syndrome | Focal Segmental Glomerulosclerosis | Chronic Thromboembolic Pulmonary Hypertension | Bacterial Meningitis | Dent Disease | Kashin-Beck Disease | Porphyria, Variegate | Woodhouse-Sakati Syndrome | Hypocalcemia | Pendred Syndrome | Aromatic L-amino Acid Decarboxylase Deficiency | Glycogen Storage Disease Type 9 | Microphthalmia, Syndromic 7 | Cardiac Sarcoidosis | Spinocerebellar Ataxia | Arthritis, Psoriatic | Vaginitis | Carcinoma, Transitional Cell | Myhre Syndrome | Erdheim-Chester Disease | Richter's Syndrome | Fibrodysplasia Ossificans Progressiva | Adenomatoid Tumor | Porokeratosis | Stuve-Wiedemann Syndrome | Trichotillomania | Monilethrix | Sarcosinemia | Hypophosphatasia | Osteoglophonic Dysplasia | Chronic Myeloid Leukemia | Progressive External Ophthalmoplegia | Hemoglobinopathies | Cockayne Syndrome | Spinocerebellar Ataxia Type 10 | Seasonal Mood Disorder | Angioimmunoblastic T-cell Lymphoma | Oligoastrocytoma | Wagner Disease | Retinal Dystrophy, Early-onset Severe | Coenzyme Q10 Deficiency | Adams-Oliver Syndrome | Ulcerative Colitis | Thrombasthenia | Auriculocondylar Syndrome | Tietze Syndrome | Corneal Neovascularization | X-linked Myotubular Myopathy | VACTERL/VATER Association | Sjogren Syndrome | Echinococcosis | Idiopathic Pulmonary Fibrosis | Diabetic Macular Edema | Retinopathy Of Prematurity | Granular Corneal Dystrophy | Skin Fragility-woolly Hair Syndrome | Beckwith-Wiedemann Syndrome | Tumoral Calcinosis | Zimmermann-Laband Syndrome | Epidermolysis Bullosa Acquisita | Plasma Cell Leukemia | Thrombophlebitis | Uremic Pruritus | Acute Generalized Exanthematous Pustulosis | Turner's Syndrome | Fowler's Syndrome | Prostatitis | Contact Dermatitis | Dysequilibrium Syndrome | Sandhoff Disease | Congenital Aniridia | Communication Disorders | Acute Kidney Injury | Benign Recurrent Intrahepatic Cholestasis 1 | Conjunctivitis, Allergic | X-linked Charcot-Marie-Tooth Disease | Hidradenitis | Sporadic Hemiplegic Migraine | Shprintzen-Goldberg Syndrome | Androgen Insensitivity | Desmosterolosis | Persistent Mullerian Duct Syndrome | Duodenal Atresia | Spinocerebellar Ataxia Type 27 | Maternally Inherited Diabetes And Deafness | Bare Lymphocyte Syndrome | Spinocerebellar Ataxia Type 38 | Lipid Metabolism Disorders | Stuttering | Nephroblastoma | Spinocerebellar Ataxia Type 6 | Paraganglioma | Birk-Barel Syndrome | Microcephalic Primordial Dwarfism | Vulvovaginitis | Lymphedema | Cheilitis | Encephalitis, Tick-borne | Achromatopsia | Chediak-Higashi Syndrome | Waardenburg Syndrome | Sertoli Cell-only Syndrome | Split Hand-foot Malformation | Hashimoto Thyroiditis | Osteogenesis Imperfecta Type V | Thromboembolism | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Neurodermatitis | Epithelioid Hemangioma | Heterotopic Ossification | Greig Cephalopolysyndactyly Syndrome | Retinoblastoma | Congenital Heart Defects | Episodic Ataxia Type 1 | Alexander Disease | Vascular Calcification | Alpers Syndrome | Trimethylaminuria | PASLI Disease | GATA2 Deficiency | Cutaneous Lupus Erythematosus | Hyperoxaluria | Olmsted Syndrome | Focal Dermal Hypoplasia | Cyst | Von Hippel-Lindau Disease | Pachyonychia Congenita | Thyroiditis, Autoimmune | Gerstmann-Straussler-Scheinker Syndrome | Leishmaniasis, Visceral | Meier-Gorlin Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Endometriosis | Skin Carcinoma | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Waardenburg Syndrome Type 2 | Meniere's Disease | Cholestasis | Cardiomyopathy, Restrictive | Tic Disorder | Cancer, Bladder | Pyruvate Kinase Deficiency | Genee-Wiedemann Syndrome | Bainbridge-Ropers Syndrome | Peripheral Neuropathy | Alzheimer Disease, Late Onset | Charcot-Marie-Tooth Disease Type 2E | Endometrial Hyperplasia | Oligoasthenoteratozoospermia | Congenital Mirror Movements | Congenital Disorders Of Glycosylation Type II | Riboflavin Transporter Deficiency Neuronopathy | Aarskog-Scott Syndrome | Meningococcal Infections | Infantile Neuroaxonal Dystrophy | Stiff-man Syndrome | Chorioretinitis | ADNP Syndrome | Orotic Aciduria | Histoplasmosis | Schwannomatosis | Leri Pleonosteosis | Noonan Syndrome | Sialoadenitis | Exocrine Pancreatic Insufficiency | Twin-to-twin Transfusion Syndrome | Alopecia Totalis | Chronic Inflammatory Demyelinating Polyneuropathy | Gastroenteritis, Eosinophilic | Congenital Muscular Dystrophy | Pseudohypoaldosteronism | Amyotrophic Lateral Sclerosis, Juvenile | Holt-Oram Syndrome | Pyelonephritis | Ellis-Van Creveld Syndrome | Sotos Syndrome | Ichthyosis Bullosa Of Siemens | Iron Overload | Cri-du-chat Syndrome | Distal Myopathy 2 | Early Infantile Epileptic Encephalopathy 1 | Gout | Graves Disease | Esophagitis | Myopia | B-cell Prolymphocytic Leukemia | Synpolydactyly | Mucolipidosis | Stromal Corneal Dystrophy | Blau Syndrome | Colon Adenoma | Hepatopulmonary Syndrome | Bone Marrow Necrosis | Hartsfield Syndrome | Bicuspid Aortic Valve | Atherosclerosis | Adult Polyglucosan Body Disease | Gray Platelet Syndrome | Protein C Deficiency | Cholangiocarcinoma | Retinal Coloboma | Hypobetalipoproteinemias | Lyme Disease | Primary Progressive Aphasia | Non-bullous Congenital Ichthyosiform Erythroderma | Camurati-Engelmann Disease | Scapuloperoneal Myopathy, X-linked Dominant | Zollinger-Ellison Syndrome | Tangier Disease | Autosomal Recessive Spastic Paraplegia Type 75 | Epilepsy, Generalized | Myasthenia Gravis | Sensory Neuropathy | Stomatitis | Spondylo-ocular Syndrome | Ganglioglioma | Emery-Dreifuss Muscular Dystrophy | Presbyopia | NGLY1 Deficiency | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Osteomalacia | Autoimmune Disease | Atopic Dermatitis | Progressive Familial Intrahepatic Cholestasis Type 3 | Hypothalamic Obesity | Non-small Cell Lung Cancer | Hyperglycemia | Venous Insufficiency | Nephrotic Syndrome Type 1 | Diffuse Mesangial Sclerosis | Waardenburg Syndrome Type 4A | Osteosclerosis | Optic Nerve Diseases | Cardiomyopathy, Hypertrophic | Peroxisomal Disorder | Focal Cortical Dysplasia Type 2 | Nemaline Myopathy 10 | Crigler-Najjar Syndrome | Glanzmann Thrombasthenia | Proteus Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Geleophysic Dysplasia | Nephrocalcinosis | Corneal Ulcer | Ameloblastic Carcinoma | Placenta Previa | Pregnancy, Ectopic | Amblyopia | Dermatofibrosarcoma | Erythromelalgia | Coronary Heart Disease | Dysgerminoma | Esthesioneuroblastoma | Ureteropelvic Junction Obstruction | Relapsing Polychondritis | Aneurysm, Abdominal Aortic | Antiphospholipid Syndrome | Spinal And Bulbar Muscular Atrophy | Zellweger Syndrome | Fetal Alcohol Syndrome | Dengue Shock Syndrome | Lymphoma | Congenital Hemolytic Anemia | Behcet's Disease | Congenital Torticollis | Endometritis | Poirier-Bienvenu Neurodevelopmental Syndrome | Nemaline Myopathy | Nephronophthisis | Fontaine Progeroid Syndrome | Niemann-Pick Disease, Type A | Chronic Periodontitis | Diastrophic Dysplasia | Sialidosis | Leri-Weill Dyschondrosteosis | Angiodysplasia | Cryoglobulinemia | Pseudomyxoma Peritonei | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Wolfram Syndrome 2 | Melanocytic Nevus | Chiari Malformation Type I | Charcot-Marie-Tooth Disease Type 2D | Hypoproteinemia, Hypercatabolic | Kawasaki Disease | Hemorrhagic Disorders | Wiskott-Aldrich Syndrome | Acute Motor Axonal Neuropathy | Mesothelioma, Malignant | Pierpont Syndrome | Myoclonic Atonic Epilepsy | Diabetic Encephalopathy | Transcobalamin Deficiency | Glioblastoma | Anxiety Disorders | Spinocerebellar Ataxia Type 31 | Mastitis | Congenital Myasthenic Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Bullous Pemphigoid | ICF Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Multiple Sclerosis, Primary Progressive | Acute Coronary Syndrome | Knobloch Syndrome | Coloboma | Epidermolysis Bullosa Simplex, Localized | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Necrobiosis Lipoidica | Scleritis | Lassa Fever | Patent Ductus Arteriosus | Spinocerebellar Ataxia Type 13