Disease

Polymyositis

About the Disease
Polymyositis, also known as pm - [polymyositis], is related to inclusion body myositis and interstitial lung disease. An important gene associated with Polymyositis is RN7SL1 (RNA Component Of Signal Recognition Particle 7SL1), and among its related pathways/superpathways are miRNAs involved in DNA damage response and miRNAs involvement in the immune response in sepsis. The drugs Prednisone and Prednisolone phosphate have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, heart and bone, and related phenotypes are autoimmunity and emg abnormality

Common Targets
Interferon-alpha (IFN-alpha) (nonspecified subtype) | HOXD4 | ERBB3 | IFNA13 | GLIS3 | PSMB9 | G7015 | MC2R | CD86 | TLR9 | MS4A1 | Interleukin-12 (IL-12) | CTSG | STAT4 | LILRA4 | TNFAIP3 | BLK | MIR146A | PRTN3 | WT1 | IRF5 | HOXB1 | CD80 | Immunoproteasome | S1PR5 | IL12A | IFIH1 | GLP1R | IFNAR1 | TLR7 | S1PR1 | HLA-DRB1 | PSMB8 | ELANE | HLA-B | IFNAR2 | IL12B | TLR8 | Interleukin 23 complex (IL-23) | HOXC11 | TYK2 | EMX2 | ALX4 | HOXD3

疾病靶点研报
Polymyositis

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

Other Diseases

Lipoma | Corneal Dystrophy | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Schwartz-Jampel-Aberfeld Syndrome | Smith-Magenis Syndrome | Hyperlipidemia | Riboflavin Transporter Deficiency Neuronopathy | Juvenile Myelomonocytic Leukemia | Facioscapulohumeral Muscular Dystrophy Type 2 | Galactosialidosis | Acquired Partial Lipodystrophy | Lymphangioma | Gerstmann-Straussler-Scheinker Syndrome | Cyclic Vomiting Syndrome | Inflammatory Linear Verrucous Epidermal Nevus | Vertebrobasilar Insufficiency | Spondylometaphyseal Dysplasia | Thrombophlebitis | Binge Eating Disorder | Neuromyelitis Optica | Carcinoma, Signet Ring Cell | Pyruvate Carboxylase Deficiency Disease | Cholangitis | Giant Cell Arteritis | Vitelliform Macular Dystrophy | Macrodactyly | Leukocyte Adhesion Deficiency | Osteochondrosis | Glycogen Storage Disease Type 4 | Leri Pleonosteosis | Blomstrand Osteochondrodysplasia | GNE Myopathy | Mitochondrial DNA Depletion Syndrome | Genee-Wiedemann Syndrome | Waardenburg Syndrome Type 1 | Retinoblastoma | Cutis Laxa | Infectious Diarrhea | Apparent Mineralocorticoid Excess Syndrome | Giant Cell Glioblastoma | Vitamin D Deficiency | Succinic Semialdehyde Dehydrogenase Deficiency | Osteomalacia | DNA Ligase IV Deficiency | Acrodermatitis | Polymyositis | Syncope | Tyrosinemia | Meniere's Disease | Osteochondroma | Rett Syndrome | Cutaneous T-cell Lymphoma | Nance-Horan Syndrome | Niemann-Pick Disease, Type C | Pneumoconiosis | Metabolic Diseases | Polydactyly | Familial Cerebral Amyloid Angiopathy | Congenital Hemolytic Anemia | Diffuse Intrinsic Pontine Glioma | Enlarged Vestibular Aqueduct | Leukemia | Acrocallosal Syndrome | Sleep Disorder | Bullous Pemphigoid | Duane Retraction Syndrome | Shprintzen-Goldberg Syndrome | Lassa Fever | Macular Corneal Dystrophy | Neurofibromatosis Type 2 | Hypocalcemia | Retinopathy, Diabetic | Nemaline Myopathy 8 | Acute Coronary Syndrome | Cystitis | Veno-occlusive Disease | LMNA-related Congenital Muscular Dystrophy | Gout | Gastric Atrophy | Cluster Headache | Lymphoma, Mantle Cell | Schuurs-Hoeijmakers Syndrome | X-linked Sideroblastic Anemia | Lymphoma, AIDS-related | Seizures-scoliosis-macrocephaly Syndrome | Subcortical Band Heterotopia | Micropenis | Supravalvular Aortic Stenosis | Lymphangioleiomyomatosis | Hemosiderosis | Reticular Dysgenesis | Thyroiditis | Heart Block | Cryptorchidism | Dominant Optic Atrophy | Hyperferritinemia-cataract Syndrome | Congestive Heart Failure | Gilbert Syndrome | Cirrhosis | Spinocerebellar Ataxia Type 14 | Hepatic Adenomatosis | Language Disorders | Antenatal Bartter Syndrome Type 1 | Optic Neuropathy, Anterior Ischemic | Triphalangeal Thumb-polysyndactyly Syndrome | Megalencephaly | Myofibrillar Myopathy | Neurotoxicity | Lateral Meningocele Syndrome | Rhabdomyosarcoma, Embryonal | Coma | Kawasaki Disease | Spinocerebellar Ataxia Type 28 | Amblyopia | Pyloric Stenosis, Infantile Hypertrophic | Fukuyama Congenital Muscular Dystrophy | Episodic Ataxia Type 2 | Heroin Dependence | Currarino Syndrome | Wolfram Syndrome | Myhre Syndrome | LEOPARD Syndrome | Ocular Hypertension | Uremia | Corneal Ulcer | Donnai-Barrow Syndrome | Cherubism | Miyoshi Myopathy | Gliosarcoma | Superficial Spreading Melanoma | Prolidase Deficiency | Chronic Thromboembolic Pulmonary Hypertension | Liver Failure | Infantile Nephropathic Cystinosis | Bronchiectasis | Thrombosis | Charcot-Marie-Tooth Disease, Type 6 | Hypercalciuria | Melanoma, Uveal | Opisthorchiasis | Waardenburg Syndrome | Mood Disorder | Ichthyosis Bullosa Of Siemens | Ollier Disease | Myocarditis | Charcot-Marie-Tooth Disease Type 4D | Bietti Crystalline Dystrophy | Familial Dysautonomia | Oligoasthenoteratozoospermia | Cleidocranial Dysplasia | Angiosarcoma | Netherton Syndrome | Congenital Myopathy | Focal Dermal Hypoplasia | Primary Hyperoxaluria Type 3 | Neuroma | Aldosteronism | Martsolf Syndrome | Spinocerebellar Ataxia Type 5 | Non-Hodgkin Lymphoma | Dysthymia | Delayed Sleep Phase Syndrome | Aneurysm, Abdominal Aortic | Primary Aldosteronism | Neurofibromatosis Type 1 | Chorioretinitis | Alpha-1 Antitrypsin Deficiency | Pure Autonomic Failure | Centronuclear Myopathy | Light Chain Amyloidosis | Osteoglophonic Dysplasia | Early Infantile Epileptic Encephalopathy 28 | Spinocerebellar Ataxia Type 15 | Hereditary Mixed Polyposis Syndrome | Hyperinsulinism-hyperammonemia Syndrome | Glycogen Storage Disease Type 9 | Muir-Torre Syndrome | Raynaud Phenomenon | Congenital Absence Of Vas Deferens | Loeys-Dietz Syndrome Type 4 | Greenberg Dysplasia | Galactosemia | Ebstein Anomaly | Paroxysmal Kinesigenic Dyskinesia | Cramp Fasciculation Syndrome | FG Syndrome | Discoid Lupus Erythematosus | Hydrocephalus | Hereditary Elliptocytosis | Dental Caries | Lymphomatoid Granulomatosis | Epidermolytic Ichthyosis, Annular | Hepatorenal Syndrome | Endometritis | Pre-eclampsia | Bethlem Myopathy | Proctitis | Molybdenum Cofactor Deficiency | Nemaline Myopathy 10 | Optic Nerve Hypoplasia, Bilateral | Turner's Syndrome | Fahr Disease | Phenylketonuria II | Sarcosinemia | Blue Rubber Bleb Nevus Syndrome | Diabetic Encephalopathy | Polymicrogyria | Periodic Limb Movement Disorder | Otopalatodigital Syndrome Type 2 | Low Phospholipid Associated Cholelithiasis | Angiodysplasia | Hyperinsulinemic Hypoglycemia | Allan-Herndon-Dudley Syndrome | Tinea Versicolor | Hennekam Lymphangiectasia-lymphedema Syndrome | Fuchs Dystrophy | Schistosomiasis | Rotor Syndrome | Autoimmune Disease | Spinal Muscular Atrophy Type 2 | Delirium | Jalili Syndrome | Pineoblastoma | Diabetes Gestational | Otitis Externa | Speech Disorders | Menetrier Disease | Vitamin K Deficiency | Osteoporosis-pseudoglioma Syndrome | NDH Syndrome | Adrenomyeloneuropathy | Hemangioendothelioma | Tatton-Brown-Rahman Syndrome | Amyotrophic Lateral Sclerosis, Juvenile | Hypolipoproteinemia | Pseudohypoparathyroidism Type 1C | Epilepsy Of Infancy With Migrating Focal Seizures | Lysosomal Acid Lipase Deficiency | Acromicric Dysplasia | Primrose Syndrome | Diverticulitis | X-linked Acrogigantism | Hepatitis A | Anuria | DRESS Syndrome | Peeling Skin Syndrome Type B | Wagner Disease | Leigh Syndrome | Sensorineural Hearing Loss | Bardet-Biedl Syndrome | Diffuse Mesangial Sclerosis | Hypersensitivity Pneumonitis | Poirier-Bienvenu Neurodevelopmental Syndrome | Inflammatory Bowel Disease | Richter's Syndrome | Sengers Syndrome | Esthesioneuroblastoma | Williams Syndrome | Varicocele | Smith-Kingsmore Syndrome | Dyslexia | Crimean-Congo Hemorrhagic Fever | Uveitis | Withdrawal Syndrome | COACH Syndrome | Silver-Russell Syndrome | Malignant Fibrous Histiocytoma | Adenoma, Pleomorphic | Babesiosis | Chronic Neutrophilic Leukemia | N-acetylglutamate Synthase Deficiency | Sleep Apnea, Obstructive | Liddle Syndrome | Ectrodactyly | Lupus Erythematosus | Mountain Sickness | Vitreoretinal Degeneration, Snowflake Type | Palmoplantar Keratoderma | Carney Triad | Hemangioma | Werner's Syndrome | Monilethrix | Tietze Syndrome | Carpal Tunnel Syndrome | Retinal Vasculitis | Zellweger Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Antiphospholipid Syndrome | Ornithine Transcarbamylase Deficiency | Hypotonia-cystinuria Syndrome | Fibrosarcoma | Pulmonary Vein Stenosis | Lentigo | Giant Axonal Neuropathy | Dyggve-Melchior-Clausen Disease | Hepatitis, Autoimmune | Congenital Aniridia | Tuberculous Meningitis | Mabry Syndrome | Migraine | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Usher Syndrome | Asperger Syndrome | Benign Familial Infantile Seizures | Keratosis, Seborrheic | Retinal Detachment | Triple A Syndrome | Necrotizing Autoimmune Myopathy | Spondylocostal Dysostosis | Sporadic Hemiplegic Migraine | Rhizomelic Chondrodysplasia Punctata | Congenital Stromal Corneal Dystrophy | Central Core Disease | Antisynthetase Syndrome | Nicolaides-Baraitser Syndrome | Progressive Familial Intrahepatic Cholestasis Type 1 | Schizoaffective Disorder | Tyrosinemia Type 1 | Papillorenal Syndrome | Whipple's Disease | Pseudomyxoma Peritonei | Dementia | Infertility, Male | Nemaline Myopathy | Klinefelter Syndrome | Farber Disease | Adenomatoid Tumor | Craniolenticulosutural Dysplasia | Alopecia | Alpha-thalassemia Myelodysplasia Syndrome | Mucormycosis | Hepatitis B, Chronic | Hypohidrotic Ectodermal Dysplasia, X-linked | Renal Tubular Acidosis | Dystonia Musculorum Deformans | Liver Failure, Acute Infantile | Gangliosidosis | Hereditary Pyropoikilocytosis | Palsy, Cerebral | Retinal Degeneration | Swine Influenza | Sarcoma | Lymphoma Lymphoblastic | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Corneal Dystrophies, Hereditary | Peeling Skin Syndrome, Acral Type | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Congenital Myasthenic Syndrome | NGLY1 Deficiency | Cranioectodermal Dysplasia | Pemphigus Foliaceus | Ataxia-hypogonadism-choroidal Dystrophy Syndrome | Macular Degeneration | Multicystic Renal Dysplasia | Hypogonadism | Hereditary Spastic Paraplegia | Blepharophimosis Syndrome | Hyperparathyroidism, Secondary | Hepatitis E | Wiedemann-Steiner Syndrome | Glanzmann Thrombasthenia | Congenital Ichthyosiform Erythroderma | Hyperuricemia | Sarcoma, Ewing | Torticollis | Pneumonia, Mycoplasma | Neuroendocrine Cancer | Localized Scleroderma | Haim-Munk Syndrome | Corneal Edema | Benign Familial Neonatal Convulsions | Thrombocythemia, Essential | Papilloma | Kaposiform Hemangioendothelioma | Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia | Adenoma, Villous | Dystrophy, Cone-rod | Intellectual Disability, Autosomal Dominant 5 | Hartnup Disease | Congenital Bilateral Absence Of Vas Deferens | Ghosal Syndrome | Erythema Nodosum | IgA Deficiency | Asthma, Exercise-induced | Usher Syndrome Type III | Diarrhea | Meningitis | Cerebellar Ataxia, Cayman Type | Fundus Albipunctatus | Benign Familial Pemphigus | Paraganglioma | Nephrotic Syndrome Type 1 | Crisponi Syndrome | Specific Granule Deficiency | Creatine Deficiency Syndrome | IgA Nephropathy | Ophthalmia, Sympathetic | Spinocerebellar Ataxia Type 31 | Polycystic Kidney, Autosomal Recessive | T-cell Prolymphocytic Leukemia