Disease

Adenomyosis

About the Disease
Adenomyosis, also known as endometriosis of uterus, is related to leiomyoma and adenomyoma. An important gene associated with Adenomyosis is ESR1 (Estrogen Receptor 1), and among its related pathways/superpathways are ERK Signaling and GPCR Pathway. The drugs Oxytocin and Acetaminophen have been mentioned in the context of this disorder. Affiliated tissues include uterus, ovary and neutrophil, and related phenotypes are abnormal bleeding and dysmenorrhea

Common Targets
RHOJ | TMEM132C | MED13 | LMF1 | NR3C1 | PADI2 | PIK3CA | PMVK | PPM1F | ABHD8 | RRAGA | PGR | ITGA2 | SCN3A | GLYATL3 | HIPK1 | PGS1 | PPP2R1A | OSGIN1 | NLRP5 | CUZD1 | MKNK1 | ABCG1 | KIF4A | RAB40B | G367 | NHS | ZNF445 | OXT | G3845 | KIAA1671 | MYADML2 | TTC21A | SH3BP4 | LSP1 | ZNF207 | SMPDL3B | GPR27 | RBBP8 | ST6GAL2 | ZNG1C | AJAP1 | KMT2D | ATP13A4 | ZNF512B | UNC5A | TSPYL2 | SNAPC1 | C1QTNF6 | ZNF565 | OXTR | MMP1 | ARHGAP42 | PRKACA | FER1L6 | UTP14A | PLXNB3 | HIF1A | OR51D1 | C12orf42 | LIPG | CCDC168 | NBPF10 | NPAP1 | ZNF468 | CR2 | GNA12 | OR5M10 | KIAA1755 | RAET1G | MXRA5

疾病靶点研报
Adenomyosis

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

Other Diseases

Colitis | Spinocerebellar Ataxia Type 5 | IMAGe Syndrome | Cancer, Prostate | Uveitis, Anterior | Dementia, Vascular | Infantile Nephropathic Cystinosis | Eclampsia | Fabry's Disease | Optic Atrophy 2 | Neuromyelitis Optica | Scoliosis | Mucolipidosis | Woodhouse-Sakati Syndrome | Central Retinal Artery Occlusion | Torticollis | Diabetes Mellitus, Transient Neonatal | Vitamin A Deficiency | Schistosomiasis | Syndactyly | Coloboma | Tyrosine Hydroxylase Deficiency | Necrotizing Autoimmune Myopathy | Epidermolysis Bullosa Acquisita | Actinomycetoma | Ichthyosis Bullosa Of Siemens | Rolandic Epilepsy | IgA Deficiency | Erysipelas | Hereditary Spastic Paraplegia | Alkaptonuria | Waardenburg Syndrome | Fanconi Anemia | Measles | Zollinger-Ellison Syndrome | Crohn's Disease | Hamartoma | Marfan Syndrome | Stroke | Pulmonary Vein Stenosis | Retinoschisis | Cranial Nerve Disease | Lung Diseases | Autosomal Recessive Spastic Paraplegia Type 35 | Corneal Dystrophies, Hereditary | Mucolipidosis Type IV | Anorexia Nervosa | Lymphangioma | Non-bullous Congenital Ichthyosiform Erythroderma | Dominant Optic Atrophy | Asthma | Rash | Pupil Disorders | Galloway-Mowat Syndrome | Sialoadenitis | Systemic Lupus Erythematosus | Congenital Mirror Movements | Ganglioneuroma | Chronic Periodontitis | Neurodevelopmental Disorders | Toxoplasmosis | Exocrine Pancreatic Insufficiency | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Infectious Diarrhea | Juvenile Polyposis | Charcot-Marie-Tooth Disease, Type 2C | Keratopathy | Obesity | C3 Glomerulopathy | Mitochondrial Cytopathy | Muckle-Wells Syndrome | Milk Allergy | Silicosis | DRESS Syndrome | Melanocytic Nevus | Hidradenitis | Androgenic Alopecia | Pierpont Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Lattice Corneal Dystrophy | Pulmonary Veno-occlusive Disease | Hemorrhagic Disorders | Congenital Bilateral Absence Of Vas Deferens | Migraine | T-cell Lymphoma, Subcutaneous Panniculitis-like | Nicotine Addiction | Progressive Familial Intrahepatic Cholestasis Type 2 | Non-Hodgkin Lymphoma | Heart Block | CEDNIK Syndrome | Charcot-Marie-Tooth Disease Type 3 | Progressive Osseous Heteroplasia | Hemochromatosis Type 2 | Plasmacytoma | Macular Degeneration | Amyotrophic Lateral Sclerosis | Benign Hereditary Chorea | Kabuki Syndrome | Liver Diseases | Mitochondrial DNA Depletion Syndrome, Myopathic Form | HUPRA Syndrome | Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy | Cutaneous T-cell Lymphoma | Scapuloperoneal Spinal Muscular Atrophy | Lateral Meningocele Syndrome | Pseudomyxoma Peritonei | Bardet-Biedl Syndrome | Stuve-Wiedemann Syndrome | Avian Influenza | Epidermolysis Bullosa Simplex, Generalized | Sialidosis | Polyomavirus Nephropathy | Xeroderma Pigmentosum | Krabbe Disease | Sulfite Oxidase Deficiency | Dengue Shock Syndrome | Heterotaxy | Hyperferritinemia-cataract Syndrome | Chylothorax, Congenital | Epilepsy Of Infancy With Migrating Focal Seizures | Osteopathia Striata With Cranial Sclerosis | Asthma, Exercise-induced | Cutaneous Angiosarcoma | Neonatal Progeroid Syndrome | Encephalopathy, Glycine | Carey-Fineman-Ziter Syndrome | Primary Biliary Cholangitis | Anterior Segment Dysgenesis | Chronic Kidney Disease | Opisthorchiasis | Burn-McKeown Syndrome | Glaucoma | Gestational Trophoblastic Disease | Sarcoma | Renal Medullary Carcinoma | Hyperacusis | Hypermetropia | Neuronal Ceroid Lipofuscinosis | Cholestasis, Intrahepatic | Rhabdomyosarcoma, Alveolar | Avellino Corneal Dystrophy | Chromosome 5q Deletion Syndrome | Combined Pituitary Hormone Deficiency | Lipid Storage Diseases | Spinocerebellar Ataxia Type 16 | Pre-eclampsia | Vitreoretinopathy, Proliferative | Benign Familial Infantile Seizures | Periventricular Leukomalacia | Dupuytren Disease | Temtamy Preaxial Brachydactyly Syndrome | X-linked Acrogigantism | Pemphigoid | Borjeson-Forssman-Lehmann Syndrome | Progressive Myoclonic Epilepsy | Hyperinsulinemia | Split Hand-foot Malformation | Nephrotic Syndrome Type 1 | Rubeosis Iridis | Dysthymia | Urea Cycle Disorder | Carney-Stratakis Syndrome | Porphyria, Variegate | Zimmermann-Laband Syndrome | Osteomalacia | Dermatofibrosarcoma | Takayasu's Arteritis | Goiter, Nodular | Arteriovenous Malformations | Hypotonia-cystinuria Syndrome | AIDS | Myopia | Exostoses | Nance-Horan Syndrome | Spinocerebellar Ataxia Type 10 | Pseudohypoaldosteronism | Pseudo-pseudohypoparathyroidism | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Sarcoma, Alveolar Soft Part | Polymyalgia Rheumatica | Gigantism | Dysequilibrium Syndrome | Myositis, Focal | McLeod Syndrome | Uremic Pruritus | Graft-versus-host Disease | Glutaric Aciduria Type 2 | Heart Septal Defects | Optic Nerve Diseases | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Gangliosidosis, GM1 | Juvenile Myelomonocytic Leukemia | Spinal Muscular Atrophy Type 3 | Glioma | Pain | Syphilis | Multiple Epiphyseal Dysplasia | Transcobalamin Deficiency | Muscle Wasting | Keratocystic Odontogenic Tumor | Cardiomyopathy, Restrictive | Hypertensive Retinopathy | Liddle Syndrome | Amyotrophic Lateral Sclerosis, Juvenile | Hypopituitarism | Perivascular Epithelioid Cell Tumor | Hypoalbuminemia | Autoimmune Disease | Cranioectodermal Dysplasia | Neurofibromatosis-Noonan Syndrome | Personality Disorders | Absence Epilepsy | Peyronie's Disease | Lyme Disease | Multicentric Carpotarsal Osteolysis Syndrome | Idiopathic Multicentric Castleman Disease | Mitochondrial DNA Depletion Syndrome, Encephalomyopathic Form | Monilethrix | Congenital Generalized Lipodystrophy | Retinal Degeneration | Angiomyolipoma | Hypotension, Orthostatic | Acne | Axenfeld-Rieger Syndrome | Tuberculous Meningitis | Malignant Fibrous Histiocytoma | Osteoglophonic Dysplasia | Bronchitis | Esophageal Motility Disorders | Colon Adenoma | Open-angle Glaucoma | Bacterial Meningitis | Tibial Muscular Dystrophy | Myelomeningocele | Primary Ovarian Insufficiency | Mood Disorder | Spinal Cord Diseases | Craniometaphyseal Dysplasia | Arthropathy | Microtia | X-linked Myotubular Myopathy | Gnathodiaphyseal Dysplasia | Desmosterolosis | Hypohidrotic Ectodermal Dysplasia | Herpes Simplex Dermatitis | Pemphigus Foliaceus | Hypocalcemia | Diverticulitis | Dysferlinopathy | Tyrosinemia | Protein S Deficiency | Lattice Corneal Dystrophy Type 1 | Metachromatic Leukodystrophy | Subcortical Band Heterotopia | Huntington's Disease-like 2 | Tinea | Sezary Syndrome | Polycystic Kidney, Autosomal Recessive | Porphyria | Primary Lateral Sclerosis | Angiodysplasia | Thyroiditis, Autoimmune | Chiari Malformation Type I | Ocular Hypertension | Sertoli Cell-only Syndrome | Familial Male-limited Precocious Puberty | Nephrocalcinosis | Depression | Biotinidase Deficiency | Becker Muscular Dystrophy | Epithelioid Hemangioma | Lymphoma Lymphoblastic | Spinocerebellar Ataxia Type 13 | Retinopathy, Diabetic | Epidermolysis Bullosa Simplex, Localized | Carbamoyl Phosphate Synthetase I Deficiency | Hyperammonemia | GLUT1 Deficiency Syndrome | Spinal Muscular Atrophy Type 2 | Retinal Detachment | Polycystic Liver | Tietze Syndrome | Empyema | Bernard-Soulier Syndrome | Seizures | Li-Fraumeni Syndrome | Walker-Warburg Syndrome | Hairy Cell Leukemia | Cancer, Lung | Behcet's Disease | Eczema | Partington Syndrome | Peutz-Jeghers Syndrome | Insulinoma | Neuromuscular Disorders | Diabetes Type 2 | Peritonitis | Atelosteogenesis Type 2 | Chronic Leukemia | Discoid Lupus Erythematosus | Thanatophoric Dysplasia Type 1 | LMNA-related Congenital Muscular Dystrophy | Osteogenesis Imperfecta | Corneal Edema | Rubinstein-Taybi Syndrome | Delirium | Spinocerebellar Ataxia Type 6 | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | Fibromuscular Dysplasia | Hyperostosis | Periventricular Nodular Heterotopia | Hypercalcemia | SAPHO Syndrome | Coronary Restenosis | Hypercalciuria | Olmsted Syndrome | Pilomatrix Carcinoma | Steel Syndrome | Lactose Intolerance | Vitiligo | Osteogenesis Imperfecta Type IV | Familial Mediterranean Fever | Encephalitis, Tick-borne | Renal-hepatic-pancreatic Dysplasia | Cysticercosis | Aspergillosis | Duodenal Atresia | Hyperparathyroidism | Lamellar Ichthyosis | Familial Cerebral Amyloid Angiopathy | Megaloblastic Anemia | Snyder-Robinson Syndrome | Fragile X Syndrome | Hartnup Disease | Hoyeraal-Hreidarsson Syndrome | Kawasaki Disease | Thin Basement Membrane Disease | Botulism | Donnai-Barrow Syndrome | Sorsby Fundus Dystrophy | Gerstmann-Straussler-Scheinker Syndrome | Asperger Syndrome | Galactosialidosis | Mitochondrial DNA Depletion Syndrome | Membranous Nephropathy | Atopy | Adenomyosis | Primary Hyperoxaluria | Hydrocephalus | Amebiasis | Diabetes Gestational | Keratosis | Pneumococcal Meningitis | Glycogen Storage Disease | Basal Ganglia Disease | Facioscapulohumeral Muscular Dystrophy Type 2 | Chondrodysplasia Punctata | Cryptosporidiosis | Pontocerebellar Hypoplasia Type 2 | Focal Facial Dermal Dysplasia | Panniculitis | Dermatitis | Diamond-Blackfan Anemia | Glycogen Storage Disease Type 5 | Lymphoproliferative Disease, X-linked | Lymphedema | Gray Platelet Syndrome | Chromosome 8q21.11 Deletion Syndrome | Von Willebrand Disease | Large Granular Lymphocytic Leukemia | Primary Familial Brain Calcification | Cryptococcal Meningitis | Behavioral Variant Of Frontotemporal Dementia | Congenital Adrenal Hyperplasia 1 | Cerebrovascular Disorders | Retinal Vasculitis | Conjunctivitis, Allergic | Anemia | Primary Cutaneous Amyloidosis | Antithrombin III Deficiency | Gynecomastia | Scleroderma, Diffuse | Apraxia | Cirrhosis | Primary Aldosteronism | Kearns-Sayre Syndrome | Guttate Psoriasis | ICF Syndrome | Familial Hypertrophic Cardiomyopathy | Nephrosclerosis | Neuroleptic Malignant Syndrome | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Renal Tubular Acidosis | Waardenburg Syndrome Type 2E | Seizures-scoliosis-macrocephaly Syndrome | Cholecystitis | Congenital Hemolytic Anemia | Priapism | Supravalvular Aortic Stenosis | Presbyopia