Mycoplasma Pneumonia

About the Disease
Mycoplasma Pneumoniae Pneumonia, also known as mycoplasmal pneumonia, is related to adult respiratory distress syndrome and haemophilus influenzae. An important gene associated with Mycoplasma Pneumoniae Pneumonia is CRP (C-Reactive Protein), and among its related pathways/superpathways are Innate Immune System and ERK Signaling. The drugs Levofloxacin and Ofloxacin have been mentioned in the context of this disorder. Affiliated tissues include lung, bone marrow and neutrophil, and related phenotypes are digestive/alimentary and immune system

Common Targets
ACE | CD276 | G7099

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

Other Diseases

Coronary Restenosis | Alexander Disease | Twin-to-twin Transfusion Syndrome | Neurocysticercosis | Corneal Neovascularization | Woodhouse-Sakati Syndrome | Globozoospermia | Anuria | Coronary Heart Disease | Renal Hypouricemia | Hidradenitis Suppurativa | Pneumoconiosis | Hypolipoproteinemia | Proximal Symphalangism | Cranioectodermal Dysplasia | Mabry Syndrome | Osteitis | Postaxial Polydactyly | Best Macular Dystrophy | Colitis | Ameloblastic Carcinoma | Limb Girdle Muscular Dystrophy | Carey-Fineman-Ziter Syndrome | Hartnup Disease | Acanthosis Nigricans | Congenital Afibrinogenemia | Homocystinuria | SAPHO Syndrome | Chorea | Coronary Artery Disease | Exfoliative Dermatitis | TARP Syndrome | Intellectual Disability, Autosomal Dominant 5 | Spondylosis | Mountain Sickness | Esophageal Carcinoma | Chiari Malformation Type I | Schizotypal Personality Disorder | Crohn's Disease | Congenital Bile Acid Synthesis Defect | Mumps | Blue Nevus | Diabetes Insipidus, Nephrogenic | Carpal Tunnel Syndrome | Precocious Puberty | Alopecia Areata | Fowler's Syndrome | Chronic Lymphocytic Leukemia | Hyperhomocysteinemia | Geleophysic Dysplasia | Carcinoma, Transitional Cell | Hypoplastic Left Heart Syndrome | Swine Influenza | Metanephric Adenoma | Mucolipidosis Type II | Gastric Atrophy | Leiomyosarcoma | Acute Myeloid Leukemia | Mitochondrial Myopathy | Interstitial Lung Diseases | Fanconi Anemia | Dysmorphophobia | Scapuloperoneal Myopathy, X-linked Dominant | Tenosynovial Giant Cell Tumor | Syphilis | Reye Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Cranial Nerve Disease | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | 3-methylglutaconic Aciduria | Porphyria | Anti-glomerular Basement Membrane Disease | Smith-Magenis Syndrome | Oligospermia | Dwarfism | Spinocerebellar Ataxia | Hemolytic Uremic Syndrome, Atypical | Focal Segmental Glomerulosclerosis | Hyperparathyroidism-jaw Tumor Syndrome | HIBCH Deficiency | Stroke, Ischemic | Cheilitis | Dysgerminoma | Agnathia-Otocephaly Complex | Membranous Nephropathy | Cerebrovascular Disorders | Heart Septal Defects | Light Chain Amyloidosis | Glycogen Storage Disease Type 0, Muscle | Craniolenticulosutural Dysplasia | Microcephaly | Neutropenia | Adenomatoid Tumor | Myopathy | Juvenile Myoclonic Epilepsy | Restless Legs Syndrome | Multicentric Carpotarsal Osteolysis Syndrome | Trichuriasis | Short-chain Acyl-CoA Dehydrogenase Deficiency | Esophageal Adenocarcinoma | Milk Allergy | Niemann-Pick Disease, Type B | Parkinsonism | Netherton Syndrome | Mucolipidosis | Mitochondrial DNA Depletion Syndrome 13 | Spinocerebellar Ataxia Type 42 | Stargardt Disease | Stuve-Wiedemann Syndrome | Centronuclear Myopathy | Cancer, Breast | Takotsubo Cardiomyopathy | Atelosteogenesis Type 1 | Familial Partial Lipodystrophy | Lymphoma Lymphoblastic | Persistent Mullerian Duct Syndrome | Polyneuropathy | Oculodentodigital Dysplasia | Multiple Mitochondrial Dysfunctions Syndrome Type 1 | Primary Torsion Dystonia | Coloboma | Delirium | Thrombosis | Chronic Idiopathic Myelofibrosis | Antiphospholipid Syndrome | Familial Isolated Hyperparathyroidism | Galloway-Mowat Syndrome | Hyperostosis | Kawasaki Disease | Maple Syrup Urine Disease | LMNA-related Congenital Muscular Dystrophy | D-2-Hydroxyglutaric Aciduria | Duane Retraction Syndrome | Gastrointestinal Disorders | Glycogen Storage Disease Type 4 | Myhre Syndrome | Frank-ter Haar Syndrome | Neutrophilia | Psoriasis | Thrombocytopenia | 3-methylglutaconic Aciduria Type I | Seasonal Mood Disorder | 3C Syndrome | Megaloblastic Anemia | Von Hippel-Lindau Disease | Schwannomatosis | Hydrops Fetalis | Hyperandrogenemia | Sleep Disorder | Torticollis | Cohen Syndrome | Vitreoretinal Degeneration, Snowflake Type | Pityriasis Rubra Pilaris | Palsy, Cerebral | Pulmonary Alveolar Proteinosis | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Heroin Dependence | Wilson's Disease | Erythematotelangiectatic Rosacea | Hyperlipidemia, Familial Combined | Blomstrand Osteochondrodysplasia | Liebenberg Syndrome | LEOPARD Syndrome | Carbohydrate Metabolism Disorders | Pemphigus Vulgaris | Acrodysostosis | Keratocystic Odontogenic Tumor | Ehlers-Danlos Syndrome With Progressive Kyphoscoliosis, Myopathy, And Hearing Loss | Meningioma | Kallmann Syndrome | Spinal And Bulbar Muscular Atrophy | Chondrodysplasia Punctata 2, X-linked Dominant | Hypotension, Orthostatic | Sleep Apnea | Angiosarcoma Of The Breast | Paternal Uniparental Disomy Of Chromosome 14 | Mohr-Tranebjaerg Syndrome | Essential Fructosuria | Carney-Stratakis Syndrome | Pulmonary Sclerosing Hemangioma | Tic Disorder | Vitamin D Deficiency | Pouchitis | Sepiapterin Reductase Deficiency | Exostoses | Neuromuscular Disorders | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hypersomnia | Blau Syndrome | Asthma, Exercise-induced | Miyoshi Myopathy | Waardenburg Syndrome Type 2E | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Ehlers-Danlos Syndrome | Cholelithiasis | Pathological Gambling | Vitamin A Deficiency | Protein S Deficiency | Thalassemia, Beta | Congenital Fiber-type Disproportion Myopathy | Gastroenteritis, Eosinophilic | Behavioral Variant Of Frontotemporal Dementia | Diarrhea | Triphalangeal Thumb-polysyndactyly Syndrome | Lattice Corneal Dystrophy Type 1 | Urethritis | Zygomycosis | Malnutrition | Loeys-Dietz Syndrome Type 4 | Atopic Dermatitis | Riboflavin Transporter Deficiency Neuronopathy | Pierre Robin Syndrome | Keratoacanthoma | Pyruvate Carboxylase Deficiency Disease | Spinocerebellar Ataxia Type 6 | Sickle Cell Disease | Snyder-Robinson Syndrome | Rotor Syndrome | Migraine | Imerslund-Grasbeck Syndrome | Infertility | Eosinophilia | Retinal Degeneration | Hypoalbuminemia | Hyperbilirubinemia | Multiple Sclerosis, Chronic Progressive | Obesity, Morbid | Iron Overload | HELLP Syndrome | Anterior Segment Dysgenesis | Generalized Epilepsy And Paroxysmal Dyskinesia | Mandibuloacral Dysplasia With Type A Lipodystrophy | Palmoplantar Keratoderma | Sclerosing Cholangitis | Chondromyxoid Fibroma | Schwartz-Jampel-Aberfeld Syndrome | Colitis, Collagenous | Microphthalmia, Syndromic 7 | Micropenis | Raynaud Phenomenon | Borderline Personality Disorder | HANAC Syndrome | Hemorrhage | Waardenburg Syndrome Type 1 | Mixed Connective Tissue Disease | 5-oxoprolinase Deficiency | Roberts Syndrome | Jawad Syndrome | Odonto-onycho-dermal Dysplasia | Charcot-Marie-Tooth Disease Type 4E | Hypertelorism | Progressive Familial Intrahepatic Cholestasis Type 2 | Aphasia | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Alstrom Syndrome | Osteochondroma | Chordoma | Behcet's Disease | Adenoma, Pituitary | Speech Disorders | Erdheim-Chester Disease | Pregnancy, Ectopic | Episodic Ataxia Type 2 | Acute Lymphocytic Leukemia | Duodenal Atresia | Renal Failure | Intracerebral Hemorrhage | Perry Syndrome | Personality Disorders | Spinocerebellar Ataxia Type 15 | Pleural Tuberculosis | Cystinosis | Jacobsen Syndrome | Chudley-McCullough Syndrome | Li-Fraumeni Syndrome | Neural Tube Defect | T-cell Lymphoma, Subcutaneous Panniculitis-like | Hepatic Veno-occlusive Disease | Orthostatic Intolerance | Ichthyosis, X-linked | Hyperprolactinemia | Pulmonary Capillary Hemangiomatosis | Blastomycosis | Angiodysplasia | Infantile Spasm | Brenner Tumor | Mucolipidosis Type IV | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Graves Disease | Mitochondrial DNA Depletion Syndrome | Cocaine-Related Disorders | Cherubism | Congenital Disorders Of Glycosylation | Lymphoma | Ophthalmia, Sympathetic | Neuroma | Congenital Aniridia | Keloid | Sialoadenitis | Conjunctivitis, Allergic | Calcium Pyrophosphate Deposition Disease | Sclerosteosis | Dystonia | Primary Biliary Cholangitis | Keratosis, Actinic | Juvenile Myelomonocytic Leukemia | Nail Disorder, Nonsyndromic Congenital | T-cell Chronic Lymphocytic Leukemia | Bardet-Biedl Syndrome | Hyperkalemic Periodic Paralysis | Discoid Lupus Erythematosus | Ichthyosis | Hemimegalencephaly | Acrocallosal Syndrome | Sporadic Hemiplegic Migraine | Hypertension, Pulmonary | Hyperinsulinemia | Anti-NMDA Receptor Encephalitis | Cantu Syndrome | Cerebral Cavernous Malformations | Micro Syndrome | Familial Hypertrophic Cardiomyopathy | Cutaneous T-cell Lymphoma | Contact Dermatitis | Poirier-Bienvenu Neurodevelopmental Syndrome | Retinopathy, Diabetic | Encephalopathy, Glycine | Hereditary Spastic Paraplegia | Hemangioendothelioma | Tuberculosis | Gynecomastia | Emery-Dreifuss Muscular Dystrophy | Cardiac Sarcoidosis | Aneurysm, Thoracic Aortic | Pneumothorax | Okihiro Syndrome | Glycogen Storage Disease Type 5 | Myoclonic Epilepsy With Ragged Red Fibers | Carney Triad | Cerebellar Ataxia, Cayman Type | Chromosome 9q34.3 Deletion Syndrome | Myoclonus | Atherosclerosis | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Persistent Hyperplastic Primary Vitreous | Myoclonus-dystonia Syndrome | Pseudo-pseudohypoparathyroidism | Coenzyme Q10 Deficiency | Infectious Diarrhea | Antenatal Bartter Syndrome Type 1 | Spinocerebellar Ataxia Type 27 | Nicotine Addiction | Chordoid Glioma | Thanatophoric Dysplasia Type 1 | Focal Dermal Hypoplasia | Porencephaly | Supravalvular Aortic Stenosis | Congenital Torticollis | Epithelioid Hemangioma | Arthritis, Reactive | Menkes Disease | Adenoma, Villous | Asphyxia Neonatorum | Anovulation | Melnick-Needles Syndrome | Vasculitis | Pain | Congenital Dyserythropoietic Anemia Type 4 | Spinal Muscular Atrophy | Guillain-Barre Syndrome | Wagner Disease | Encephalopathy | Camurati-Engelmann Disease | Pre-eclampsia | Sitosterolemia | Central Pain Syndrome | Proctitis | Cancer, Prostate | Giant Cell Arteritis | Osteoglophonic Dysplasia | Tibial Muscular Dystrophy | Takenouchi-Kosaki Syndrome | Tracheal Disorders | Gastritis, Atrophic | Gitelman Syndrome | Cataplexy | Seminoma | Facioscapulohumeral Muscular Dystrophy Type 2 | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Polyomavirus Nephropathy | Castleman Disease | Lymphoma, B-cell | Cancer, Kidney | Otosclerosis | Multiple Sclerosis, Primary Progressive | Retinoblastoma | Craniosynostosis | Neovascular Glaucoma | Early Infantile Epileptic Encephalopathy | Subcortical Band Heterotopia