Disease

Dermatomyositis

About the Disease
Dermatomyositis, also known as amyopathic dermatomyositis, is related to inclusion body myositis and interstitial lung disease, and has symptoms including exanthema and pruritus. An important gene associated with Dermatomyositis is RN7SL1 (RNA Component Of Signal Recognition Particle 7SL1), and among its related pathways/superpathways are miRNAs involvement in the immune response in sepsis and miRNAs involved in DNA damage response. The drugs Pirfenidone and Cyclophosphamide have been mentioned in the context of this disorder. Affiliated tissues include muscle, skin where a skin rash is often seen prior to the onset of muscle weakness and skin, and related phenotypes are autoimmunity and emg abnormality

Common Targets
Lipoxygenase (nonspecified subtype) | IL1B | ERBB3 | IL17RA | IFNB1 | GLIS3 | IL10 | PSMB9 | SYK | G3605 | G7015 | MC2R | RASGRP3 | ATG16L1 | CD86 | TLR9 | JAK2 | MS4A1 | Interleukin-12 (IL-12) | CTSG | CXCL12 | STAT4 | LILRA4 | SLC15A4 | JAK1 | TNFAIP3 | JAK3 | MBL2 | BLK | MIR146A | PRTN3 | IRF5 | ANKRD55 | HLA-DQB1 | CD80 | Immunoproteasome | HLA-DPB1 | S1PR5 | IL12A | IFIH1 | STING1 | GLP1R | ALB | S1PR1 | TLR7 | HLA-DRB1 | PSMB8 | ELANE | CNR2 | ARHGAP31 | RORC | Phosphodiesterase IV (PDE4) (nonspecified subtype) | IL12B | TLR8 | Interleukin 23 complex (IL-23) | TYK2 | G2099 | G5743 | C5 | G3569 | IL2RA | G7852 | G7124

疾病靶点研报
Dermatomyositis

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

Other Diseases

Adenomatoid Tumor | Ovarian Sex Cord-stromal Tumor | Pouchitis | Cerebrovascular Disorders | Familial Isolated Hyperparathyroidism | Chronic Periodontitis | Graft-versus-host Disease | Iron Deficiency Anemia | Nicotine Addiction | Depression | Spinocerebellar Ataxia Type 7 | Alcoholism | Photosensitivity | Hypohidrotic Ectodermal Dysplasia | Hypolipoproteinemia | Hypertension | Ureteropelvic Junction Obstruction | Goiter, Nodular | Kaposiform Hemangioendothelioma | Partington Syndrome | TARP Syndrome | Neuroleptic Malignant Syndrome | Alstrom Syndrome | Epidermolysis Bullosa Acquisita | DOCK8 Immunodeficiency Syndrome | Diamond-Blackfan Anemia | Waardenburg Syndrome Type 2A | Ataxia-ocular Apraxia 2 | Conjunctivitis | Pycnodysostosis | Congenital Aniridia | Arthrogryposis | Rhabdoid Tumor | Spinocerebellar Ataxia Type 8 | Gout | Congenital Dyserythropoietic Anemia Type 4 | Infantile Liver Failure Syndrome 1 | Impulse Control Disorder | Autoimmune Hemolytic Anemia | Pain | Dominant Optic Atrophy | Rotor Syndrome | Macular Corneal Dystrophy Type 1 | Splenomegaly | Cri-du-chat Syndrome | Trimethylaminuria | Infertility | Spinocerebellar Ataxia Type 31 | Anorectal Fistula | Constipation | Hypobetalipoproteinemias | Weill-Marchesani Syndrome | Hyperlipidemia | Spinocerebellar Ataxia Type 40 | Tetraplegia | Anti-NMDA Receptor Encephalitis | McLeod Syndrome | Neuroma | Persistent Mullerian Duct Syndrome | Tonsillitis | Familial Advanced Sleep Phase Syndrome | Melanoma | 3-methylglutaconic Aciduria Type IV | Stroke, Ischemic | Duchenne Muscular Dystrophy | Myocardial Infarction | Gaucher Disease | Arthritis, Reactive | Riboflavin Transporter Deficiency Neuronopathy | Erythematotelangiectatic Rosacea | Steel Syndrome | Lymphomatoid Granulomatosis | Thymoma, Malignant | Glycogen Storage Disease Type 9 | Cornelia De Lange Syndrome | Creutzfeldt-Jakob Disease | Arthritis | Loeys-Dietz Syndrome | Asthma, Exercise-induced | Nemaline Myopathy 8 | Hypervalinemia | Blepharophimosis Syndrome | Obsessive-compulsive Disorder | Acute Leukemia | Fuchs Heterochromic Iridocyclitis | Retinal Coloboma | Bacterial Meningitis | Dystonia | Hepatitis D | Dengue Shock Syndrome | Poretti-Boltshauser Syndrome | Dyslexia | Cartilage Disorders | Shock, Cardiogenic | Glioblastoma Multiforme | X-linked Charcot-Marie-Tooth Disease | Chronic Kidney Disease | Hemorrhage | Dermatitis Herpetiformis | Hyperkalemic Periodic Paralysis | Juvenile Myelomonocytic Leukemia | Cataract | Cerebral Amyloid Angiopathy | Liver Failure, Acute Infantile | Mesothelioma, Malignant | Schwannoma | Thyroid Dysgenesis | Hydrocephalus, Normal Pressure | Multiple Sclerosis, Chronic Progressive | Seizures | Craniolenticulosutural Dysplasia | Charcot-Marie-Tooth Disease Axonal Type 2N | Anencephaly | Mucolipidosis | Spinocerebellar Ataxia Type 5 | Alopecia Totalis | Hyperammonemia | Protein C Deficiency | Schnyder Crystalline Corneal Dystrophy | Coenzyme Q10 Deficiency | Charcot-Marie-Tooth Disease, Type 1A | Nanophthalmos | Hashimoto Thyroiditis | Alkaptonuria | Meckel-Gruber Syndrome | Diastrophic Dysplasia | Primary Progressive Aphasia | Idiopathic Multicentric Castleman Disease | Spinocerebellar Ataxia Type 12 | Cerebellofaciodental Syndrome | Lymphoproliferative Disorders | Vici Syndrome | Synovitis | Congenital Absence Of Vas Deferens | Multiple Myeloma | Nephrocalcinosis | Vaginitis | Growth Hormone Excess | Dermatitis | Temtamy Preaxial Brachydactyly Syndrome | Otitis Externa | Niemann-Pick Disease, Type B | Twin-to-twin Transfusion Syndrome | Parkinson's Disease | Hypertrophy | Cannabis Abuse | Colitis | Sickle Cell Anemia | Familial Cerebral Amyloid Angiopathy | Hyperostosis | Aldosteronism | Charcot-Marie-Tooth Disease Type 4E | Pregnancy, Ectopic | Hyperbilirubinemia | Chronic Myeloid Leukemia | Familial Retinal Arterial Macroaneurysm | Meesmann Corneal Dystrophy | Granular Corneal Dystrophy | Klinefelter Syndrome | Congenital Muscular Dystrophy | Hepatitis, Alcoholic | Angioedema, Acquired | Glaucoma | C3 Glomerulonephritis | Congenital Lipoid Adrenal Hyperplasia | Small Lymphocytic Lymphoma | Osteogenesis Imperfecta Type III | Ileitis | Palmoplantar Keratoderma | Eiken Syndrome | Johanson-Blizzard Syndrome | Adrenoleukodystrophy, X-linked | Parkinson Disease 6, Autosomal Recessive Early-onset | Blepharitis | Atrioventricular Septal Defect | Peripheral T-cell Lymphoma | Mitochondrial Cytopathy | Cystitis | Gallstones | Cholera | Amelanotic Melanoma | Greenberg Dysplasia | Dementia | Nail Disorder, Nonsyndromic Congenital | Multiple Sclerosis, Primary Progressive | Personality Disorders | Cutaneous T-cell Lymphoma | Heroin Dependence | Relapsing Polychondritis | Malaria | Hepatitis | Focal Facial Dermal Dysplasia | Cerebrotendinous Xanthomatosis | Optic Neuropathy | Proteasome-associated Autoinflammatory Syndrome 2 | Primary Lateral Sclerosis | Sertoli Cell-only Syndrome | Leber Hereditary Optic Neuropathy | Wolfram Syndrome | Pneumococcal Meningitis | Spinocerebellar Ataxia Type 28 | IgA Deficiency | Microvillus Inclusion Disease | Leishmaniasis, Cutaneous | Presbyopia | Usher Syndrome Type IIC | VACTERL/VATER Association | Progressive Familial Intrahepatic Cholestasis Type 3 | Chondroma | Cystitis, Interstitial | Richter's Syndrome | Acquired Partial Lipodystrophy | Malonyl-CoA Decarboxylase Deficiency | Congenital Bile Acid Synthesis Defect | Obesity | Charcot-Marie-Tooth Disease Type 4D | Autosomal Recessive Bestrophinopathy | Primary Biliary Cholangitis | Neural Tube Defect | Multicystic Renal Dysplasia | Medulloblastoma | Muscle Wasting | Diabetic Nephropathy | Aspergillosis | Peroxisomal Disorder | Myotonia | Diarrhea | Diabetes Gestational | Pituitary Disorders | Lymphopenia | Dysferlinopathy | Gastroenteritis | Central Retinal Artery Occlusion | Bladder Exstrophy | Wolcott-Rallison Syndrome | T-cell Chronic Lymphocytic Leukemia | Extramammary Paget's Disease | Contact Dermatitis | Kernicterus | Mycosis Fungoides | Apert Syndrome | Neutrophilia | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Oculocutaneous Albinism Type 1 | Myositis | Renpenning Syndrome | Hepatitis, Autoimmune | Leukemia-lymphoma, Adult T-cell | Familial Male-limited Precocious Puberty | Adenocarcinoma | Endometrial Hyperplasia | Anuria | Arthritis, Psoriatic | Angiomyolipoma | Alzheimer Disease, Late Onset | Genitopatellar Syndrome | Autosomal Recessive Spastic Paraplegia Type 54 | Hemorrhagic Disorders | Menetrier Disease | Myelomeningocele | LEOPARD Syndrome | Cardiofaciocutaneous Syndrome | Heart Septal Defects | Craniopharyngioma | X-linked Creatine Transporter Deficiency | Albinism | GAPO Syndrome | Sialidosis Type I | Charcot-Marie-Tooth Disease, Type 2 | Meningioma | Corneal Edema | Guanidinoacetate Methyltransferase Deficiency | GNE Myopathy | Sweet Syndrome | Eosinophilic Asthma | Blepharoconjunctivitis | Cockayne Syndrome | CDKL5 Deficiency Disorder | Congenital Heart Defects | Geleophysic Dysplasia | VEXAS Syndrome | Gingivitis | Roberts Syndrome | Pulmonary Sclerosing Hemangioma | Congenital Dysfibrinogenemia | GM2-gangliosidosis AB Variant | Schaaf-Yang Syndrome | Hypothyroidism | Chronic Beryllium Disease | Congenital Adrenal Hyperplasia | Carcinoma, Transitional Cell | Infantile Spasm | Androgenic Alopecia | Fatty Aldehyde Dehydrogenase Deficiency | Osteonecrosis Of The Jaw | Shprintzen-Goldberg Syndrome | Disseminated Intravascular Coagulation | Pilomatrix Carcinoma | Limb Girdle Muscular Dystrophy | Atherosclerosis | Erythema Nodosum | Impetigo | Aneurysm, Abdominal Aortic | Microcephalic Primordial Dwarfism | Rubinstein-Taybi Syndrome | Carpenter Syndrome | Insulin Resistance | Glutaric Aciduria Type 2 | Camurati-Engelmann Disease | Oguchi Disease-2 | Dystrophy, Cone-rod | Central Pain Syndrome | High Molecular Weight Kininogen Deficiency | Sturge-Weber Syndrome | Arterial Tortuosity Syndrome | Aldosterone Synthase Deficiency | Large Granular Lymphocytic Leukemia | Aplasia Cutis Congenita | Pneumonia, Mycoplasma | Spermatocele | Galloway-Mowat Syndrome | Silicosis | Granular Corneal Dystrophy Type 1 | Mabry Syndrome | Transcobalamin Deficiency | Prune Belly Syndrome | Sulfite Oxidase Deficiency | Isobutyryl-CoA Dehydrogenase Deficiency | Epicondylitis | Ocular Albinism Type 1 | Ectrodactyly | Noonan Syndrome-like Disorder With Loose Anagen Hair | Cancer, Lung | Meningococcal Meningitis | Cavitary Optic Disc Anomalies | Hemimegalencephaly | Amish Infantile Epilepsy Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Infantile Refsum Disease | Pompe Disease | Uterine Leiomyoma | Giant Cell Arteritis | Retinoschisis | Salla Disease | Spitz Nevus | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Pitt-Hopkins Syndrome | Borderline Personality Disorder | Pterygium | Phenylketonuria II | Waardenburg Syndrome Type 4 | Corneal Ulcer | Encephalitis, Tick-borne | Hypermethioninemia | Hyperinsulinemic Hypoglycemia | Gynecomastia | Dyggve-Melchior-Clausen Disease | Cousin Syndrome | Osteoporosis | Neurocutaneous Melanocytosis | Wagner Disease | Antisynthetase Syndrome | GLUT1 Deficiency Syndrome | Pupil Disorders | Coma | Cholestasis, Intrahepatic | Erythema Multiforme | Cancer, Bladder | Fibrodysplasia Ossificans Progressiva | Esophageal Adenocarcinoma | Dyskeratosis Congenita | Inflammatory Myopathy | Stargardt Disease | Seizures-scoliosis-macrocephaly Syndrome | Spinocerebellar Ataxia | Ichthyosis, X-linked | Acromegaly | Isovaleric Acidemia | Hyperphenylalaninemia | Histiocytosis | Neurofibrosarcoma | Gardner Syndrome | Rhizomelic Chondrodysplasia Punctata | Sengers Syndrome | Pierson Syndrome | Persistent Hyperplastic Primary Vitreous | Blau Syndrome | Stuve-Wiedemann Syndrome | Low Tension Glaucoma | Thrombophlebitis | Werner's Syndrome | Cancer, Brain | Intellectual Disability, Autosomal Dominant 5 | Congestive Heart Failure | Wieacker-Wolff Syndrome | Congenital Hypofibrinogenemia | Hyperacusis | Methylmalonic Aciduria And Homocystinuria, CblC Type | Porphyria, Variegate | Leukoencephalopathy, Progressive Multifocal