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

Bare Lymphocyte Syndrome | Crohn's Disease | Granuloma Annulare | Systemic Mastocytosis | Fragile X Syndrome | Mesothelioma, Malignant | Amelogenesis Imperfecta | Immunoproliferative Disorders | McKusick Type Metaphyseal Chondrodysplasia | Non-Langerhans Cell Histiocytosis | Asthma, Exercise-induced | Lennox-Gastaut Syndrome | Ehlers-Danlos Syndrome | Prostatitis | Meleda Disease | Pseudohypoparathyroidism Type 1A | Craniofrontonasal Syndrome | Retinitis Pigmentosa 3 | Chylothorax, Congenital | Chanarin-Dorfman Syndrome | Adrenomyeloneuropathy | Periventricular Nodular Heterotopia | Bronchitis, Chronic | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Hashimoto Thyroiditis | Conduct Disorder | Werner's Syndrome | Retinal Dystrophy, Early-onset Severe | Multicentric Carpotarsal Osteolysis Syndrome | Cancer, Bladder | Mucolipidosis | Congenital Heart Defects | Hepatic Veno-occlusive Disease | Moyamoya Disease | Metatropic Dysplasia | Epidermodysplasia Verruciformis | Sarcomatoid Carcinoma Of The Lung | Kashin-Beck Disease | Chronic Leukemia | Plasmacytoma | Hyperoxaluria | TARP Syndrome | Tay-Sachs Disease | Optic Nerve Diseases | Acute Coronary Syndrome | Best Macular Dystrophy | Lattice Corneal Dystrophy | Heroin Dependence | Sjogren Syndrome | Kaposiform Hemangioendothelioma | Apert Syndrome | Diabetes Gestational | Discoid Lupus Erythematosus | Glioma | Waldenstrom Macroglobulinemia | Encephalocele | Hyperinsulinism-hyperammonemia Syndrome | Trichuriasis | Kabuki Syndrome 2 | Aplastic Anemia | Rett Syndrome | Shwachman-Bodian-Diamond Syndrome | B-cell Chronic Lymphocytic Leukemia | Pheochromocytoma | Fetal And Neonatal Alloimmune Thrombocytopenia | Fuchs Heterochromic Iridocyclitis | Urofacial Syndrome | Frank-ter Haar Syndrome | Ectrodactyly | Multiple Epiphyseal Dysplasia | Tardive Dyskinesia | B-cell Prolymphocytic Leukemia | Craniofacial Dysostosis | Glioblastoma | Cone Dystrophy | Giant Cell Arteritis | Anal Fissure | Alexander Disease | Axenfeld-Rieger Syndrome | Congenital Muscular Dystrophy | Achondrogenesis | Fahr Disease | Polycythemia Vera | Charcot-Marie-Tooth Disease, Type 2A | Galactosemia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Fowler's Syndrome | Lipodystrophy | Nicotine Addiction | Syndactyly | Alveolar Capillary Dysplasia | Hepatitis, Autoimmune | Amyotrophic Lateral Sclerosis, Juvenile | Carcinoma, Merkel Cell | Hernia, Inguinal | Generalized Epilepsy With Febrile Seizures Plus | Familial Advanced Sleep Phase Syndrome | Peeling Skin Syndrome Type B | Hypothyroidism | Corneal Dystrophy And Perceptive Deafness | Lymphangiomatosis | Pure Autonomic Failure | Osteitis | Cushing Syndrome | Obesity, Morbid | Arteriovenous Malformations | Keratosis | Treacher Collins Syndrome | Cysticercosis | Choroideremia | Porphyria | Richter's Syndrome | Adenomatoid Tumor | Progressive Familial Intrahepatic Cholestasis Type 3 | Silver-Russell Syndrome | Carbonic Anhydrase VA Deficiency | Tuberculosis | Niemann-Pick Disease, Type C | Kleine-Levin Syndrome | Craniosynostosis | Dent Disease | COACH Syndrome | Guillain-Barre Syndrome | Sarcoma, Endometrial Stromal | Pituitary Dwarfism | Spinocerebellar Ataxia Type 3 | Presbyopia | Juvenile Xanthogranuloma | Androgen Insensitivity | Otitis Externa | Erythromelalgia | Conn Syndrome | Common Cold | Iron Metabolism Disorders | Genitopatellar Syndrome | Stargardt Disease | Mucolipidosis Type II | Noonan Syndrome | Yellow Fever | Apparent Mineralocorticoid Excess Syndrome | Bietti Crystalline Dystrophy | Pulmonary Stenosis | Atopy | Malignant Fibrous Histiocytoma | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | HIBCH Deficiency | Diabetes Insipidus, Nephrogenic | Gray Platelet Syndrome | Pemphigus | Angina Pectoris | Angioimmunoblastic T-cell Lymphoma | Restless Legs Syndrome | Thrombophilia | Temporal Lobe Epilepsy | Rothmund-Thomson Syndrome | Chronic Granulomatous Disease, X-linked | Harlequin Ichthyosis | Tibial Muscular Dystrophy | Lipoma | Chronic Kidney Disease | Nemaline Myopathy | Absence Epilepsy | Sweet Syndrome | Systemic Lupus Erythematosus | Feingold Syndrome | Fibronectin Glomerulopathy | Scapuloperoneal Spinal Muscular Atrophy | Gangliosidosis | Tyrosinemia Type 1 | Spinocerebellar Ataxia Type 13 | Methylmalonic Acidemia | Anorchia | Prolymphocytic Leukemia | Familial Isolated Hyperparathyroidism | Osteoglophonic Dysplasia | Lichen Planus | Spinocerebellar Ataxia Type 31 | Mucolipidosis Type III | Hereditary Hemorrhagic Telangiectasia | Anodontia | Nephrocalcinosis | Congenital Adrenal Hyperplasia 1 | Myasthenia | Pulmonary Capillary Hemangiomatosis | D-2-Hydroxyglutaric Aciduria | Diffuse Palmoplantar Keratoderma | T-cell Prolymphocytic Leukemia | Succinic Semialdehyde Dehydrogenase Deficiency | 3-hydroxy-3-methylglutaryl-CoA Synthase Deficiency | Neurofibromatosis | Agoraphobia | Alpha-1 Antitrypsin Deficiency | Dementia | Dupuytren Disease | Congenital Primary Aphakia | Sitosterolemia | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Spinocerebellar Ataxia | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Epidermolytic Palmoplantar Keratoderma | Hereditary Xerocytosis | Multiple Sclerosis, Chronic Progressive | Crouzon Syndrome With Acanthosis Nigricans | Micropenis | Retinopathy, Diabetic | Aspergillosis | Pitt-Hopkins Syndrome | Encephalopathy, Ethylmalonic | Fanconi Syndrome | Contact Dermatitis | Amebiasis | Sickle Cell Disease | Overactive Bladder | Keratoconjunctivitis | Hyperhomocysteinemia | Thanatophoric Dysplasia | Spitzoid Melanoma | REM Sleep Behavior Disorder | Cardiac Sarcoidosis | Hypertension, Portal | Cancer, Breast | Hydrops Fetalis | Heavy Chain Disease | Seborrheic Dermatitis | Nutrition Disorders | Encephalitis, Tick-borne | Sclerosing Cholangitis | Babesiosis | Sleep Apnea, Central | Prurigo Nodularis | Congenital Stromal Corneal Dystrophy | Optic Neuritis | Histiocytosis | Ischemia | Polyarteritis Nodosa | Long QT Syndrome Type 1 | Neurofibromatosis Type 1 | L-2-Hydroxyglutaric Aciduria | Vaginitis | Angiosarcoma | Oguchi Disease-2 | Rhizomelic Chondrodysplasia Punctata | Mastitis | Cousin Syndrome | Farber Disease | Spondyloepiphyseal Dysplasia Tarda, X-linked | Hereditary Multiple Exostoses | Corneal Dystrophies, Hereditary | Mycosis Fungoides | Phenylketonuria | Proctitis | Schuurs-Hoeijmakers Syndrome | Hypoplastic Left Heart Syndrome | Congenital Dyserythropoietic Anemia | Disseminated Intravascular Coagulation | Dyggve-Melchior-Clausen Disease | Cryopyrin-associated Periodic Syndromes | Tic Disorder | Lafora Disease | AIDS | Asthma, Nocturnal | Dyslipidemia | Chronic Mucocutaneous Candidiasis | Thrombosis | Goiter | Premature Ejaculation | Trichomegaly | Osteogenesis Imperfecta | Stuttering | Fascioliasis | Benign Familial Infantile Seizures | Alpha-thalassemia Myelodysplasia Syndrome | Liver Failure | Glomerulonephritis, Membranous | Jalili Syndrome | Primary Familial Brain Calcification | Myelofibrosis | Arterial Tortuosity Syndrome | Ichthyosis | Cholestasis, Intrahepatic | Gynecomastia | Hyperuricemic Nephropathy, Familial Juvenile | Pityriasis Rubra Pilaris | Inborn Errors Of Metabolism | Trachoma | Mosaic Variegated Aneuploidy Syndrome 2 | Hereditary Sensory And Autonomic Neuropathy | Epidermolysis Bullosa Simplex | Dermatitis Herpetiformis | Chronic Inflammatory Demyelinating Polyneuropathy | Epidermolytic Hyperkeratosis | LEOPARD Syndrome | Hypersensitivity | NDH Syndrome | Alkaptonuria | Metanephric Adenoma | Hyperlipidemia | Exotropia | Hereditary Coproporphyria | Chudley-McCullough Syndrome | Lymphopenia | Cystinosis | Cardiomyopathy, Hypertrophic | Okihiro Syndrome | Mitochondrial Disease | Twin-to-twin Transfusion Syndrome | Thyrotoxic Periodic Paralysis | Polycystic Liver | Carcinoma, Squamous Cell | Leber Hereditary Optic Neuropathy | Retinitis | Usher Syndrome Type IIC | Autoimmune Disease | Alazami Syndrome | Microcephaly | VACTERL Association | Hypobetalipoproteinemias | Corneal Ulcer | Opisthorchiasis | Anosmia, Congenital | Cyclic Vomiting Syndrome | Turner's Syndrome | Basal Ganglia Cerebrovascular Disease | Sarcoidosis, Pulmonary | Ellis-Van Creveld Syndrome | Pleural Tuberculosis | Congenital Dysfibrinogenemia | Osteochondroma | Autosomal Recessive Spastic Paraplegia Type 54 | Peripheral Neuropathy | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Hartnup Disease | Schnyder Crystalline Corneal Dystrophy | Liver Failure, Acute Infantile | Retinitis Pigmentosa | Hyperthermia, Malignant | Episodic Ataxia | Usher Syndrome Type II | Ataxia-ocular Apraxia 2 | Polyomavirus Nephropathy | Creutzfeldt-Jakob Disease | Arthrogryposis | Onchocerciasis | Glanzmann Thrombasthenia | Hereditary Folate Malabsorption | Maple Syrup Urine Disease | Corneal Edema | Cranial Nerve Disease | Autoimmune Autonomic Ganglionopathy | Oligoasthenoteratozoospermia | Glioblastoma Multiforme | Pyoderma Gangrenosum | Episodic Ataxia Type 1 | Dengue Hemorrhagic Fever | Depression | Sepiapterin Reductase Deficiency | Hepatic Steatosis | Tumoral Calcinosis | Lipid Metabolism Disorders | Osteogenesis Imperfecta Type I | Roberts Syndrome | Bulimia Nervosa | Epidermolysis Bullosa Dystrophica | Vitreoretinal Degeneration, Snowflake Type | Inflammatory Myopathy | GLUT1 Deficiency Syndrome | Sarcoma | Rhabdomyosarcoma | Distal Myopathy 2 | Glycogen Storage Disease Type 6 | Optic Nerve Hypoplasia, Bilateral | Facioscapulohumeral Muscular Dystrophy Type 1 | C3 Glomerulopathy | Diabetes Insipidus, Neurogenic | Motion Sickness | Nager Acrofacial Dysostosis | Papilledema | Aplasia Cutis Congenita | Measles | Hyperammonemia | Cutaneous Mastocytosis | Trichothiodystrophy | Adenoma, Pituitary | Compartment Syndrome | Creatine Deficiency Syndrome | Anovulation | Acute Anterior Uveitis | Familial Dysautonomia | Arteriosclerosis | Leigh Syndrome | Borjeson-Forssman-Lehmann Syndrome | Muscular Dystrophy | Galloway-Mowat Syndrome | Spondyloperipheral Dysplasia | Imerslund-Grasbeck Syndrome | Dengue Shock Syndrome | Coronary Restenosis | Coffin-Lowry Syndrome | 3-methylcrotonyl-CoA Carboxylase Deficiency | Congenital Sodium Diarrhea