Disease

Endometrial Hyperplasia

About the Disease
Endometrial Hyperplasia is related to endometrial adenocarcinoma and adenomyosis. An important gene associated with Endometrial Hyperplasia is PGR (Progesterone Receptor), and among its related pathways/superpathways are Gene expression (Transcription) and Signal Transduction. The drugs BIRC5 protein, human and Estrogens, Conjugated (USP) have been mentioned in the context of this disorder. Affiliated tissues include uterus, pituitary and ovary, and related phenotypes are no effect and no effect

Common Targets
SFRP2 | G3845 | KEAP1 | G2064 | Estrogen receptor (nonspecified subtype) | PGR | DNA Topoisomerase II (nonspecified subtype) | UBR5 | G367 | CTNNA1 | TRPC5 | NCOA2 | OSR1 | Tyrosine Kinase (nonspecified subtype) | AKR1B1 | PTENP1 | PDE5A | LIN28B | GSTP1 | NOX3 | GNRHR | KMT2D | GRM8 | BCL9 | CYP19A1 | NADPH Oxidase Complex | PIK3CG | RASSF1 | G5728 | Voltage-Gated Calcium Channel alpha-2/delta (nonspecified subtype) | AMP-activated protein kinase (AMPK) | NADPH Oxidase (nonspecified subtype) | G1956 | HS1BP3 | DKK3 | CDH13 | PTPN6 | KMT2C | G3630 | G999

疾病靶点研报
Endometrial Hyperplasia

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

Other Diseases

Esophageal Motility Disorders | Epidermolysis Bullosa Simplex | Macrodactyly | Charcot-Marie-Tooth Disease Type 4B1 | Wolman Disease | Hypersomnia | Anorexia Nervosa | Tuberculosis | Brenner Tumor | Cervicitis | Prolymphocytic Leukemia | Muckle-Wells Syndrome | Constipation | Thrombasthenia | Bronchiectasis | Schizoaffective Disorder | Dysfibrinogenemia | Interstitial Lung Diseases | 5-oxoprolinase Deficiency | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Oculocutaneous Albinism | Congenital Poikiloderma | Epidermolysis Bullosa Dystrophica | Central Core Disease | Okihiro Syndrome | Hemochromatosis Type 1 | Nutrition Disorders | Meningioma | Mucolipidosis | Esophageal Adenocarcinoma | Spinocerebellar Ataxia Type 31 | PHARC Syndrome | Congenital Adrenal Hyperplasia 1 | Neuromyotonia | Blood Protein Disorders | Proximal Symphalangism | Neuroleptic Malignant Syndrome | Osteosarcoma | Recurrent Respiratory Papillomatosis | Spinocerebellar Ataxia Type 3 | Optic Neuritis | Priapism | Hemorrhage | Immunoproliferative Disorders | Chronic Thromboembolic Pulmonary Hypertension | Ganglioglioma | Lymphoproliferative Disease, X-linked | Whipple's Disease | Pulmonary Stenosis | Xeroderma Pigmentosum | Orotic Aciduria | Intestinal Pseudo-obstruction | Blepharo-cheilo-odontic Syndrome | Microtia | Hydrocephalus, Normal Pressure | Hypopigmentation | Ebstein Anomaly | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Polyradiculopathy | Actinomycetoma | 3-methylglutaconic Aciduria Type IV | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Osteogenesis Imperfecta Type IV | Reflex Epilepsy | Postpoliomyelitis Syndrome | Pernicious Anemia | Glioblastoma | Wiskott-Aldrich Syndrome | Auriculocondylar Syndrome | Pancreatitis, Chronic | Borderline Personality Disorder | Open-angle Glaucoma | Brachial Plexus Neuropathy | Noonan Syndrome | Charcot-Marie-Tooth Disease | Myotonia | Fucosidosis | Adenomyosis | Episodic Ataxia | Hepatitis | 3-hydroxy-3-methylglutaric Aciduria | Isovaleric Acidemia | Aplastic Anemia | Cryoglobulinemia | Fibromyalgia | Huntington's Disease-like 2 | High Molecular Weight Kininogen Deficiency | Mitochondrial DNA Depletion Syndrome | Cyclic Vomiting Syndrome | Thrombocytopenia | Cocaine-Related Disorders | Retinal Diseases | Conjunctivitis | C3 Glomerulopathy | Synpolydactyly | Metabolic Syndrome | Hyperkeratosis | Duchenne Muscular Dystrophy | Renal Tubular Dysgenesis | Ischemia | Tuberculous Meningitis | Central Pain Syndrome | Chromosome 9q34.3 Deletion Syndrome | Neonatal Progeroid Syndrome | Pseudo-pseudohypoparathyroidism | Hashimoto Thyroiditis | Facioscapulohumeral Muscular Dystrophy | Periodontitis | Urticaria | Camurati-Engelmann Disease | Familial Retinal Arterial Macroaneurysm | Martsolf Syndrome | Sporadic Inclusion Body Myositis | Impulse Control Disorder | 3-M Syndrome | Anti-NMDA Receptor Encephalitis | CEDNIK Syndrome | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Donnai-Barrow Syndrome | Hypokalemic Periodic Paralysis | Cryptorchidism | Oligodendroglioma | Netherton Syndrome | Primary Lateral Sclerosis | Carcinoma, Transitional Cell | Cartilage Disorders | Sclerosing Cholangitis | Melnick-Needles Syndrome | Sandhoff Disease | Osteogenesis Imperfecta Type II | PASLI Disease | Chronic Mucocutaneous Candidiasis | Jalili Syndrome | Glioma | Charcot-Marie-Tooth Disease, Type 2C | Eosinophilia | Idiopathic Pulmonary Fibrosis | Thyroiditis | Meesmann Corneal Dystrophy | Sclerosteosis | Schizophrenia, Paranoid | Lupus Erythematosus | Gardner Syndrome | Inflammatory Bowel Disease | Short-chain Acyl-CoA Dehydrogenase Deficiency | Methylmalonic Aciduria And Homocystinuria, CblC Type | McKusick Type Metaphyseal Chondrodysplasia | Systemic Lupus Erythematosus | Angiodysplasia | Miyoshi Myopathy | Polydactyly | Retinopathy Of Prematurity | Bernard-Soulier Syndrome | Lymphomatoid Granulomatosis | Spinocerebellar Ataxia Type 2 | Bietti Crystalline Dystrophy | Multiple System Atrophy | Pierre Robin Syndrome | Trichorhinophalangeal Syndrome | Gnathodiaphyseal Dysplasia | Primary Progressive Nonfluent Aphasia | Urolithiasis | Spinal Muscular Atrophy Type 3 | Pituitary Dwarfism | Endophthalmitis | Shprintzen-Goldberg Syndrome | Histoplasmosis | Uremia | Lymphangioma | Acne Vulgaris | Adenomatoid Tumor | Meckel-Gruber Syndrome | Norrie Disease | Lichen Sclerosus | Optic Atrophy 2 | Greenberg Dysplasia | Hereditary Elliptocytosis | Glycogen Storage Disease Type 5 | Alstrom Syndrome | Pulmonary Veno-occlusive Disease | Lyme Disease | Purpura | Marinesco-Sjogren Syndrome | Filariasis | Fanconi Anemia | Familial Cerebral Amyloid Angiopathy | Asplenia | Rhabdomyosarcoma | Persistent Mullerian Duct Syndrome | Intestinal Obstruction | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Greig Cephalopolysyndactyly Syndrome | Retinal Coloboma | Glycogen Storage Disease Type 1 | Rubeosis Iridis | Sickle Cell Disease | Corneal Dystrophies, Hereditary | Sorsby Fundus Dystrophy | Sturge-Weber Syndrome | Heterotopic Ossification | Congenital Hypofibrinogenemia | Tricho-hepato-enteric Syndrome | Progressive Familial Intrahepatic Cholestasis | Von Hippel-Lindau Disease | Odonto-onycho-dermal Dysplasia | Glaucoma, Congenital | Aneurysm, Abdominal Aortic | Insulinoma | Hydronephrosis | Anovulation | Urofacial Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Familial Pheochromocytoma-paraganglioma | Mitochondrial DNA Depletion Syndrome 13 | Pendred Syndrome | Papilledema | Hepatitis C, Chronic | Vitamin D Deficiency | Spinocerebellar Ataxia Type 13 | Carbonic Anhydrase VA Deficiency | Bainbridge-Ropers Syndrome | Rhabdoid Tumor | Pituitary Disorders | Mast Cell Leukemia | Hyperostosis | Insulin Resistance | Heavy Chain Disease | Acrodermatitis | Erysipelas | Pupil Disorders | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | HUPRA Syndrome | Nemaline Myopathy | DiGeorge Syndrome | Pyruvate Carboxylase Deficiency Disease | Genee-Wiedemann Syndrome | Pigment Dispersion Syndrome | Diarrhea | Primary Familial Brain Calcification | Erythrokeratodermia Variabilis | Osteomyelitis | Congenital Adrenal Hyperplasia | Hypohidrotic Ectodermal Dysplasia, X-linked | Eclampsia | Dementia | Multiple Sclerosis, Secondary Progressive | Thrombosis | Birt-Hogg-Dube Syndrome | Cryptosporidiosis | Charcot-Marie-Tooth Disease, Type 6 | Scapuloperoneal Spinal Muscular Atrophy | Williams Syndrome | Gerodermia Osteodysplastica | Portal Vein Thrombosis | Partington Syndrome | Basal Ganglia Disease | Colitis, Lymphocytic | Fetal Alcohol Syndrome | Infectious Diarrhea | Spinocerebellar Ataxia Type 20 | Kaposi Sarcoma | Facioscapulohumeral Muscular Dystrophy Type 2 | Lipoma | Mood Disorder | Pontocerebellar Hypoplasia Type 2 | Chromosome 8q21.11 Deletion Syndrome | Fibronectin Glomerulopathy | Trichotillomania | Endocarditis | Proteasome-associated Autoinflammatory Syndrome 2 | Neurocysticercosis | Malnutrition | Thyrotoxic Periodic Paralysis | Chorea-acanthocytosis | LMNA-related Congenital Muscular Dystrophy | Frank-ter Haar Syndrome | Neuropathy | Hyperbilirubinemia, Neonatal | Glomerulonephritis, Membranoproliferative | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Autonomic Nervous System Disorders | Hemophilia | Erythema Multiforme | Encephalopathy, Ethylmalonic | Loeys-Dietz Syndrome Type 4 | Gaucher Disease | Becker Muscular Dystrophy | Chronic Inflammatory Demyelinating Polyneuropathy | Plasma Cell Leukemia | Spastic Paraplegia Type 7 | Dyslexia | Vertigo | Scapuloperoneal Myopathy, X-linked Dominant | Torticollis | Usher Syndrome Type II | Epidermolytic Hyperkeratosis | Myoclonic Epilepsy With Ragged Red Fibers | Xeroderma Pigmentosum Variant Type | Hyper IgE Syndrome | Sclerocornea | Peyronie's Disease | Traboulsi Syndrome | Vertebrobasilar Insufficiency | Lipid Storage Myopathy | Sezary Syndrome | Progressive Osseous Heteroplasia | Fibrosarcoma | Ligneous Conjunctivitis | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Otopalatodigital Syndrome Type 2 | Oligoastrocytoma | Rhabdomyosarcoma, Alveolar | Diabetes Gestational | Renal Hypouricemia | Bipolar Disorder | Cholangiocarcinoma | Limb Girdle Muscular Dystrophy | Microcephalic Primordial Dwarfism | Spinocerebellar Ataxia Type 6 | Epidermolysis Bullosa | Myositis, Focal | Goldenhar Syndrome | Schaaf-Yang Syndrome | Pneumonia, Mycoplasma | Lipid Metabolism Disorders | Pierson Syndrome | Pearson Syndrome | FG Syndrome | Pitt-Hopkins Syndrome | Glaucoma | Hemoglobinopathies | Melanocytic Nevus | Acquired Partial Lipodystrophy | Nestor-Guillermo Progeria Syndrome | Epidermolytic Palmoplantar Keratoderma | Rickets | Methylmalonic Acidemia | Osteogenesis Imperfecta Type V | Multiple Epiphyseal Dysplasia | Adult Polyglucosan Body Disease | Non-bullous Congenital Ichthyosiform Erythroderma | Methemoglobinemia | Hyperlipidemia Type V | Blue Rubber Bleb Nevus Syndrome | Osteoglophonic Dysplasia | Stroke, Ischemic | Cardiac Sarcoidosis | Liver Failure | Purpura, Thrombotic Thrombocytopenic | Hereditary Multiple Exostoses | Japanese Encephalitis | Cancer, Prostate | Ependymoma | Cold-induced Sweating Syndrome | Micro Syndrome | Cerebrovascular Disorders | Pemphigus Foliaceus | Sclerosteosis 2 | Encephalitis, Tick-borne | Cerebrotendinous Xanthomatosis | Chronic Idiopathic Myelofibrosis | Niemann-Pick Disease, Type A | Erdheim-Chester Disease | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Biotinidase Deficiency | Common Variable Immunodeficiency | D-2-Hydroxyglutaric Aciduria | Peutz-Jeghers Syndrome | Mevalonate Kinase Deficiency | Specific Granule Deficiency | Angiosarcoma Of The Breast | Hartsfield Syndrome | Gray Platelet Syndrome | Bardet-Biedl Syndrome | Stromal Corneal Dystrophy | Peripheral Neuropathy | Early Infantile Epileptic Encephalopathy 13 | Apparent Mineralocorticoid Excess Syndrome | Corneal Dystrophy | Vascular Calcification | Steel Syndrome | Focal Segmental Glomerulosclerosis | Keratosis | Cone Dystrophy | Exocrine Pancreatic Insufficiency | Coma | Mastitis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Microcephaly, Seizures, And Developmental Delay | Sialidosis | Aneurysm, Thoracic Aortic | Takotsubo Cardiomyopathy | Brugada Syndrome 1 | Coffin-Siris Syndrome | Retinitis Pigmentosa 3 | Cataract | Scleritis | Pulmonary Alveolar Proteinosis | Alpha-1 Antitrypsin Deficiency | Encephalopathy, Hepatic