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

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

Pulmonary Stenosis | Generalized Epilepsy And Paroxysmal Dyskinesia | Dermatofibrosarcoma | Early Infantile Epileptic Encephalopathy 13 | Salla Disease | Congestive Heart Failure | Hepatitis E | 3-methylcrotonyl-CoA Carboxylase Deficiency | Bullous Pemphigoid | Acromegaly | Bronchiectasis | Glycogen Storage Disease Type 3 | Meconium Ileus | Epiphyseal Chondrodysplasia, Miura Type | Dermatomyositis | Smoldering Myeloma | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Hydrops Fetalis | Fucosidosis | Hereditary Multiple Exostoses | Infertility | Esotropia | Demyelinating Diseases | Anti-NMDA Receptor Encephalitis | Malignant Peripheral Nerve Sheath Tumor | Pseudohermaphroditism | Hemophagocytic Lymphohistiocytosis | Pfeiffer Syndrome | Achromatopsia | Hypopigmentation | Alpha-mannosidosis | Intracranial Hypertension | Juvenile Myelomonocytic Leukemia | Language Disorders | Tyrosinemia Type 1 | Crimean-Congo Hemorrhagic Fever | Craniofrontonasal Syndrome | Persistent Mullerian Duct Syndrome | Diabetes Type 1 | Spinal Cord Diseases | Apparent Mineralocorticoid Excess Syndrome | Hoyeraal-Hreidarsson Syndrome | Kaposi Sarcoma | Intestinal Hypomagnesemia 1 | Hyperparathyroidism | Urofacial Syndrome | Sclerosing Cholangitis | Motion Sickness | Herpes Genitalis | Focal Dermal Hypoplasia | Hereditary Elliptocytosis | Ebstein Anomaly | Branchiootorenal Syndrome | Hemorrhage | Long QT Syndrome Type 1 | Corneal Dystrophy | Rickets | Klippel-Feil Syndrome | COACH Syndrome | Hyperglycemia | Senior-Loken Syndrome | Osteogenesis Imperfecta Type II | Retinitis Pigmentosa | Gyrate Atrophy Of The Choroid And Retina | Acute Myeloid Leukemia | Multiple Sclerosis, Secondary Progressive | Gerodermia Osteodysplastica | Bronchiolitis | Postpartum Depression | Megaloblastic Anemia | Spondylolisthesis | Neurofibromatosis Type 1 | Hypopituitarism | Asthma, Nocturnal | Arthritis | Otitis Media | Cholelithiasis | Chudley-McCullough Syndrome | Hereditary Coproporphyria | Varicocele | T-cell Prolymphocytic Leukemia | Plasma Cell Leukemia | Endometrial Hyperplasia | Thyroiditis, Autoimmune | Chondrodysplasia Punctata 2, X-linked Dominant | Angiodysplasia | Congenital Diaphragmatic Hernia | Cerebrovascular Disorders | Leiomyoma | Hidradenitis | Paraganglioma, Carotid Body | Usher Syndrome Type III | Epilepsy | Hypothyroidism | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Anemia | Pseudoachondroplasia | Benign Recurrent Intrahepatic Cholestasis 1 | Noonan Syndrome | Preaxial Polydactyly | Mitochondrial Encephalomyopathy | Encephalopathy, Ethylmalonic | Charcot-Marie-Tooth Disease Type 2T | LRBA Deficiency | Chanarin-Dorfman Syndrome | Chromosome 5q Deletion Syndrome | Familial Exudative Vitreoretinopathy | Hyperlipidemia | Toxic Epidermal Necrolysis | Hereditary Neuropathy With Liability To Pressure Palsies | Epidermodysplasia Verruciformis | Cancer, Lung | Hepatic Adenomatosis | Kindler Syndrome | Autoimmune Hemolytic Anemia | Metanephric Adenoma | Spondylosis | CEDNIK Syndrome | Noonan Syndrome-like Disorder With Loose Anagen Hair | Neurofibrosarcoma | Aphasia | Carney-Stratakis Syndrome | Pierre Robin Syndrome | Spastic Paraplegia Type 7 | Combined Deficiency Of Factor V And Factor VIII | Congenital Generalized Lipodystrophy | GAPO Syndrome | Woodhouse-Sakati Syndrome | Pulverulent Zonular Cataract | Alpha-1 Antitrypsin Deficiency | Intermittent Claudication | Metachondromatosis | Thanatophoric Dysplasia Type 1 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Pheochromocytoma | Osteopetrosis | Rheumatic Heart Disease | Brachial Plexus Neuropathy | Plasma Cell Dyscrasia | Holt-Oram Syndrome | Schizophrenia, Paranoid | Opisthorchiasis | Lymphangioleiomyomatosis | Klinefelter Syndrome | Leri-Weill Dyschondrosteosis | Hidradenitis Suppurativa | Hairy Cell Leukemia | Gastroenteritis | Juvenile Myoclonic Epilepsy | FG Syndrome | Vitamin B12 Deficiency | Camurati-Engelmann Disease | Proteasome-associated Autoinflammatory Syndrome 2 | Polyomavirus Nephropathy | Pantothenate Kinase-associated Neurodegeneration | Acute Anterior Uveitis | Beare-Stevenson Syndrome | Cherubism | Argininosuccinic Aciduria | Empyema | Adenoma, Pituitary | Disseminated Superficial Actinic Porokeratosis | Diabetic Macular Edema | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Thrombocytopenia | HELLP Syndrome | Progressive Osseous Heteroplasia | Familial Hypertrophic Cardiomyopathy | Leishmaniasis, Cutaneous | Erectile Dysfunction | Osmotic Demyelination Syndrome | Nephrosclerosis | Ureteropelvic Junction Obstruction | Gout | Dominant Optic Atrophy | Alexander Disease | Familial Glucocorticoid Deficiency | Charcot-Marie-Tooth Disease Axonal Type 2N | Ileitis | Phenylketonuria II | Fuchs Heterochromic Iridocyclitis | Lymphoma Lymphoblastic | B-cell Prolymphocytic Leukemia | Hypertension | Adenomatoid Tumor | GATA2 Deficiency | Presbycusis | Pneumonia, Mycoplasma | Postaxial Polydactyly | Papillorenal Syndrome | Sick Sinus Syndrome | Low Tension Glaucoma | Charcot-Marie-Tooth Disease Type 4E | Chronic Thromboembolic Pulmonary Hypertension | Papillon-Lefevre Syndrome | Takenouchi-Kosaki Syndrome | Lewy Body Dementia | Basal Cell Nevus Syndrome | Acute Lung Injury | GM2-gangliosidosis AB Variant | Schizophrenia | Analgesia | Pineoblastoma | Pontocerebellar Hypoplasia | Myelitis, Transverse | Spinocerebellar Ataxia Type 40 | Rolandic Epilepsy | SAPHO Syndrome | Combined Pituitary Hormone Deficiency | IMAGe Syndrome | Asthma | Arrhythmogenic Right Ventricular Cardiomyopathy | Autism Spectrum Disorders | Whipple's Disease | Alopecia | Hodgkin Lymphoma | H Syndrome | Hypogonadism | Photosensitivity | Stroke | Fibrosarcoma | Anorectal Malformations | Pure Red Cell Aplasia | Intracerebral Hemorrhage | Major Depression | Schuurs-Hoeijmakers Syndrome | Parapsoriasis | Polyneuropathy | Leukocyte Adhesion Deficiency | Inflammatory Joint Disease | Sickle Cell Anemia | Pleomorphic Xanthoastrocytoma | Epidermolysis Bullosa Simplex With Mottled Pigmentation | Cancer, Colon | Mevalonate Kinase Deficiency | Anosmia, Congenital | Pseudomyxoma Peritonei | Systemic Mastocytosis | Adrenal Insufficiency | Charcot-Marie-Tooth Disease Type 4 | Episodic Ataxia Type 2 | Polycythemia Vera | Scapuloperoneal Myopathy, X-linked Dominant | Acute Motor Axonal Neuropathy | Nail Disorder, Nonsyndromic Congenital | Keratosis, Seborrheic | Choroiditis | Chordoma | Multiple Myeloma | Bartsocas-Papas Syndrome | Erdheim-Chester Disease | Muscle Wasting | Hemophilia | Lafora Disease | Palsy, Cerebral | Extramammary Paget's Disease | Compartment Syndrome | DRESS Syndrome | Osteoglophonic Dysplasia | HANAC Syndrome | Palmoplantar Keratoderma | X-linked Creatine Transporter Deficiency | Neurofibroma, Plexiform | Cholecystitis | Blue Nevus | Osteoarthritis | Hamartoma | Proctitis | Vulvovaginitis | VACTERL Association | Pontocerebellar Hypoplasia Type 2 | Campomelic Dysplasia | Apert Syndrome | Erythrokeratodermia Variabilis | Fetal Alcohol Syndrome | Osteomalacia | Congenital Stromal Corneal Dystrophy | Kernicterus | Angiomyolipoma | Spinal And Bulbar Muscular Atrophy | Acrodermatitis Enteropathica | Cardiomyopathy, Dilated, 1L | Saethre-Chotzen Syndrome | Congenital Heart Defects | Speech Disorders | Prostatitis | Rett Syndrome | Nicotine Dependence | Alzheimer Disease, Late Onset | Blood Protein Disorders | Atelosteogenesis Type 2 | Kleine-Levin Syndrome | Schizotypal Personality Disorder | Pyloric Stenosis, Infantile Hypertrophic | Fascioliasis | Robinow Syndrome | Thymoma, Malignant | Kashin-Beck Disease | Dubin-Johnson Syndrome | Charcot-Marie-Tooth Disease, Type 1A | Hypertriglyceridemia | Dengue Shock Syndrome | Iron Overload | Cholangiocarcinoma | Cryptosporidiosis | Congenital Bilateral Absence Of Vas Deferens | Pulmonary Alveolar Microlithiasis | Epithelial-myoepithelial Carcinoma | N-acetylglutamate Synthase Deficiency | Mitochondrial Myopathy | Congenital Muscular Dystrophy | Myelitis | Familial Thoracic Aortic Aneurysm | 3-methylglutaconic Aciduria | Celiac Disease | Restrictive Dermopathy | Infantile Spasm | Silver-Russell Syndrome | Gastric Atrophy | Pseudoexfoliation Syndrome | Cholera | Endocarditis | Scoliosis | Thyroid Dyshormonogenesis | Autoimmune Disease | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Thyroid Dysgenesis | Babesiosis | Congenital Dyserythropoietic Anemia Type 4 | Fraser Syndrome | Non-epidermolytic Palmoplantar Keratoderma | Lymphoma, AIDS-related | Hemoglobinopathies | Gastritis, Atrophic | Arthritis, Reactive | Familial Dysautonomia | Hyperekplexia | Japanese Encephalitis | Hemosiderosis | Swine Influenza | Congenital Heart Block | Heterotopic Ossification | Spondylo-ocular Syndrome | Muckle-Wells Syndrome | Miyoshi Myopathy | Hydronephrosis | Congenital Afibrinogenemia | Kabuki Syndrome 2 | Eczema | Aspartylglycosaminuria | Sepiapterin Reductase Deficiency | Keratosis, Actinic | Cranial Nerve Disease | Vitreoretinopathy, Proliferative | Glycogen Storage Disease Type 0, Muscle | Tracheal Disorders | Hyperlipidemia Type V | Spondylocarpotarsal Synostosis Syndrome | Currarino Syndrome | Thromboembolism | Prediabetes | Dysequilibrium Syndrome | Apraxia | Hereditary Mixed Polyposis Syndrome | Myelodysplasia | Relapsing Polychondritis | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Epilepsy, Generalized | Carcinoma, Merkel Cell | Keloid | Nephritis, Interstitial | Learning Disability | Thrombosis | Rheumatoid Arthritis | Chronic Kidney Disease | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Cholesteryl Ester Storage Disease | Myotonia | Spinocerebellar Ataxia Type 1 | Polymyalgia Rheumatica | Hypermetropia | Bladder Exstrophy | Angioedema, Acquired | Lissencephaly 2 | Waardenburg Syndrome Type 4A | Malaria, Cerebral | Primary Biliary Cholangitis | Restless Legs Syndrome | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Central Retinal Artery Occlusion | Albinism | Nephroblastoma | Glutaric Aciduria Type 1 | Optic Atrophy 2 | Ovarian Hyperstimulation Syndrome | Multisystemic Smooth Muscle Dysfunction Syndrome | Fibronectin Glomerulopathy | Liebenberg Syndrome | Acral Lentiginous Melanoma