Disease

Anovulation

About the Disease
Anovulation is related to hyperprolactinemia and galactorrhea. An important gene associated with Anovulation is INS (Insulin), and among its related pathways/superpathways are Signal Transduction and Metabolism of steroids. The drugs Estradiol and Polyestradiol phosphate have been mentioned in the context of this disorder. Affiliated tissues include ovary, pituitary and brain, and related phenotypes are Increased shRNA abundance (Z-score > 2) and Increased shRNA abundance (Z-score > 2)

Common Targets
FSHR | INSR | G2099 | AOPEP | VHL

疾病靶点研报
Anovulation

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

Other Diseases

Prader-Willi Syndrome | Tyrosine Hydroxylase Deficiency | Tremor | Primary Cutaneous Amyloidosis | Glycogen Storage Disease Type 1 | Vitamin D Deficiency | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Amebiasis | Congenital Fiber-type Disproportion Myopathy | Fragile X Syndrome | Stroke, Ischemic | Subacute Sclerosing Panencephalitis | Jaundice, Obstructive | Familial Hyperaldosteronism | Keratocystic Odontogenic Tumor | X-linked Charcot-Marie-Tooth Disease | Cold Agglutinin Disease | Microcephaly | Hypokalemic Periodic Paralysis | Primary Biliary Cholangitis | Pneumothorax | Osteogenesis Imperfecta Type I | Fibromuscular Dysplasia | 3-hydroxy-3-methylglutaric Aciduria | Niemann-Pick Disease, Type C | Vitamin A Deficiency | Donnai-Barrow Syndrome | Hepatitis, Autoimmune | Cousin Syndrome | Gerstmann-Straussler-Scheinker Syndrome | Neuroectodermal Tumors, Primitive | Agammaglobulinemia | Exotropia | Ectrodactyly | Cystinuria | Carcinoma, Small Cell | Lymphomatoid Granulomatosis | Pyoderma Gangrenosum | Antiphospholipid Syndrome | Pigment Dispersion Syndrome | Rash | Hypercholesterolemia, Familial | Lymphedema-distichiasis Syndrome | Conduct Disorder | Retinal Dystrophy | Avellino Corneal Dystrophy | Senior-Loken Syndrome | Diabetes | Neurocysticercosis | Primary Aldosteronism | Torticollis | Salla Disease | Werner's Syndrome | Tyrosinemia Type 1 | Cutaneous Angiosarcoma | Myosin Storage Myopathy | Carcinoma, Transitional Cell | Pure Red Cell Aplasia | Glycogen Storage Disease Type 5 | Meningococcal Infections | Major Depression | Spinocerebellar Ataxia Type 8 | Oral Lichen Planus | Kernicterus | Multicystic Renal Dysplasia | ICF Syndrome | Steel Syndrome | Cancer, Skin | Orthostatic Intolerance | Aromatic L-amino Acid Decarboxylase Deficiency | Benign Familial Pemphigus | Sarcoma, Ewing | Chromosome 8q21.11 Deletion Syndrome | Encephalopathy | McLeod Syndrome | Phenylketonuria | Usher Syndrome Type I | Migraine | Congestive Heart Failure | Cerebral Cavernous Malformations | Cholestasis, Intrahepatic | Williams Syndrome | Liebenberg Syndrome | Congenital Dyserythropoietic Anemia | Parkinson's Disease | Esophagitis, Eosinophilic | Inflammatory Myofibroblastic Tumor | Dysferlinopathy | Anxiety Disorders | Nijmegen Breakage Syndrome | Hypotrichosis Simplex | Colitis | Ventricular Septal Defect | Muir-Torre Syndrome | Encephalopathy, Glycine | Hereditary Neuropathy With Liability To Pressure Palsies | T-cell Prolymphocytic Leukemia | Goiter, Nodular | Pulmonary Capillary Hemangiomatosis | Seasonal Mood Disorder | Gliosarcoma | Feingold Syndrome | Intestinal Obstruction | Greig Cephalopolysyndactyly Syndrome | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Irritable Bowel Syndrome | Panniculitis | Learning Disability | Aldosteronism | Angelman Syndrome | Blue Rubber Bleb Nevus Syndrome | Hypotension, Orthostatic | Protein C Deficiency | Myasthenia Gravis | 3-M Syndrome | Lipid Metabolism Disorders | Krabbe Disease | Congenital Heart Block | Hypohidrotic Ectodermal Dysplasia | Aldosterone Synthase Deficiency | Hoyeraal-Hreidarsson Syndrome | Intestinal Hypomagnesemia 1 | Congenital Afibrinogenemia | Chromosome 9q34.3 Deletion Syndrome | Charcot-Marie-Tooth Disease, Type 2A | Sick Sinus Syndrome | Congenital Heart Defects | Hyperuricemic Nephropathy, Familial Juvenile | Temporal Lobe Epilepsy | Ehlers-Danlos Syndrome | Diarrhea | Overactive Bladder | Thanatophoric Dysplasia | Erythema Multiforme | Sensorineural Hearing Loss | Choroideremia | Amyloidosis | Adenocarcinoma | Desbuquois Syndrome | Congenital Nephrotic Syndrome | Left Ventricular Noncompaction | Tularemia | Hypogonadism | Paget's Disease Of The Breast | Stiff-man Syndrome | Cocaine-Related Disorders | Hepatic Veno-occlusive Disease | Mitochondrial DNA Depletion Syndrome, Myopathic Form | Pituitary Stalk Interruption Syndrome | Sotos Syndrome | Methylmalonic Acidemia | Osteoporosis | Familial Isolated Hyperparathyroidism | Pyruvate Carboxylase Deficiency Disease | Aarskog-Scott Syndrome | Mitochondrial DNA Depletion Syndrome | CHARGE Syndrome | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Hartsfield Syndrome | Dermatomyositis | Neurofibroma | Auriculocondylar Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Ichthyosis | Hydronephrosis | Pernicious Anemia | Dengue Hemorrhagic Fever | Polyomavirus Nephropathy | Acrodermatitis Enteropathica | Pendred Syndrome | Adenylosuccinate Lyase Deficiency | Shwachman-Bodian-Diamond Syndrome | Fibrosis | Polycystic Kidney, Autosomal Dominant | Adenoid Cystic Carcinoma | Optic Neuropathy | Tyrosinemia Type 2 | Usher Syndrome Type IIC | Combined Deficiency Of Factor V And Factor VIII | Autosomal Recessive Congenital Ichthyosis | B-cell Prolymphocytic Leukemia | Epilepsy Of Infancy With Migrating Focal Seizures | Carey-Fineman-Ziter Syndrome | Hereditary Xerocytosis | Lymphoma Lymphoblastic | Thyroiditis, Autoimmune | Angina Pectoris | Scleroderma, Diffuse | Delayed Sleep Phase Syndrome | Autosomal Recessive Bestrophinopathy | Pancreatitis, Chronic | Primary Carnitine Deficiency | Liver Diseases | Leukodystrophies | Congenital Poikiloderma | Impulse Control Disorder | Neurodermatitis | Malignant Fibrous Histiocytoma | Aldosterone Deficiency | Congenital Mirror Movements | Proopiomelanocortin Deficiency | Sleep Apnea, Obstructive | Congenital Disorders Of Glycosylation Type II | Fucosidosis | Acute Motor Axonal Neuropathy | Trichomegaly | Deafness, Dystonia, And Cerebral Hypomyelination | Fetal And Neonatal Alloimmune Thrombocytopenia | Epidermolytic Palmoplantar Keratoderma | Menkes Disease | Myhre Syndrome | Pseudohypoparathyroidism Type 2 | Bainbridge-Ropers Syndrome | Primary Sclerosing Cholangitis | Neurodevelopmental Disorders | Erdheim-Chester Disease | 3C Syndrome | Cushing Syndrome | Mucolipidosis Type IV | Facioscapulohumeral Muscular Dystrophy Type 1 | Glutathione Synthetase Deficiency | Polycystic Kidney, Autosomal Recessive | T-cell Lymphoma, Subcutaneous Panniculitis-like | Antithrombin III Deficiency | Ocular Surface Squamous Neoplasia | Lymphangioleiomyomatosis | Postpartum Depression | Allan-Herndon-Dudley Syndrome | Multiple System Atrophy | Triphalangeal Thumb-polysyndactyly Syndrome | Cataract | Sporadic Inclusion Body Myositis | Cataplexy | Ghosal Syndrome | Schuurs-Hoeijmakers Syndrome | Spinal And Bulbar Muscular Atrophy | Optic Atrophy 2 | Nager Acrofacial Dysostosis | Infertility, Male | Hypohidrotic Ectodermal Dysplasia, X-linked | VACTERL Association | Renal Medullary Carcinoma | Spondylo-ocular Syndrome | Orotic Aciduria | Nicolaides-Baraitser Syndrome | Tibial Muscular Dystrophy | Juvenile Myoclonic Epilepsy | Familial Male-limited Precocious Puberty | Proteasome-associated Autoinflammatory Syndrome 2 | Cone Dystrophy | Fraser Syndrome | Genitopatellar Syndrome | Iron Metabolism Disorders | Hepatitis B, Chronic | Primary Familial Brain Calcification | Connective Tissue Disorders | Hamartoma | Membranous Nephropathy | Burn-McKeown Syndrome | CHOPS Syndrome | Hemorrhagic Disorders | Sickle Cell Disease | Schwannoma | Mood Disorder | Polyneuropathy | Colitis, Lymphocytic | Fukuyama Congenital Muscular Dystrophy | Renal Oncocytoma | Ebstein Anomaly | Insulinoma | Premature Ejaculation | Sensory Neuropathy | Anterior Segment Dysgenesis | Progressive Familial Intrahepatic Cholestasis Type 2 | Acrodysostosis | Lesch-Nyhan Syndrome | Transcobalamin Deficiency | COACH Syndrome | Oculocutaneous Albinism Type 1 | Hepatic Steatosis | Coronary Restenosis | Oculocutaneous Albinism | Histoplasmosis | IgA Deficiency | Antenatal Bartter Syndrome Type 1 | Cranioectodermal Dysplasia | Antley-Bixler Syndrome | Hennekam Lymphangiectasia-lymphedema Syndrome | Cyclic Vomiting Syndrome | Lipid Storage Myopathy | Acromesomelic Dysplasia | Glycogen Storage Disease | Proximal Symphalangism | Congenital Hemolytic Anemia | Myositis, Focal | Adenomatoid Tumor | Histiocytic Sarcoma | Antisocial Personality Disorder | Pelvic Inflammatory Disease | Congenital Torticollis | Generalized Epilepsy With Febrile Seizures Plus | Episodic Ataxia Type 1 | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Charcot-Marie-Tooth Disease Type 2E | Angiomyolipoma | Hypothyroidism | GM2-gangliosidosis AB Variant | Language Disorders | Glomerulonephritis | Shock, Cardiogenic | Progressive Familial Intrahepatic Cholestasis Type 3 | Trigonocephaly | Chiari Malformation Type I | Down Syndrome | Cancer, Brain | Congenital Hereditary Endothelial Dystrophy Type I | Hypoalbuminemia | N-acetylglutamate Synthase Deficiency | Primary Progressive Nonfluent Aphasia | Retinal Diseases | Charcot-Marie-Tooth Disease Type 2T | Hereditary Sensory And Autonomic Neuropathy | Craniosynostosis | Pulmonary Vein Stenosis | Pituitary Dwarfism | Aceruloplasminemia | Cyst | Dominant Optic Atrophy | Fabry's Disease | Neuroendocrine Cancer | Hyperthyroidism | Pleural Tuberculosis | Growth Hormone Excess | Schizophrenia, Paranoid | Central Core Disease | Pulmonary Tuberculosis | Sclerosteosis 2 | Hyperacusis | Fuchs Heterochromic Iridocyclitis | PASLI Disease | Myelodysplasia | Lymphangiomatosis | Atrial Septal Defect | Diabetes Insipidus, Neurogenic | Recurrent Respiratory Papillomatosis | Microcephaly, Seizures, And Developmental Delay | Systemic Lupus Erythematosus | Episodic Ataxia Type 2 | Neural Tube Defect | T-cell Leukemia | Isovaleric Acidemia | Ichthyosis Bullosa Of Siemens | Headache | Calcium Pyrophosphate Deposition Disease | Sleep Disorder | Beckwith-Wiedemann Syndrome | Glaucoma, Congenital | Colitis, Collagenous | Heart Septal Defects | Lupus Erythematosus | Chronic Thromboembolic Pulmonary Hypertension | Whipple's Disease | Gestational Trophoblastic Disease | Polymyalgia Rheumatica | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Pheochromocytoma | Methemoglobinemia Type IV | Muscle Wasting | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Batten Disease | Meningioma | Wilson's Disease | Bare Lymphocyte Syndrome | Aphasia | Reticular Dysgenesis | Corneal Edema | Seizures-scoliosis-macrocephaly Syndrome | Neurofibromatosis-Noonan Syndrome | Emery-Dreifuss Muscular Dystrophy | Histiocytosis | Splenomegaly | Bardet-Biedl Syndrome | Bronchiectasis | Fetal Akinesia Deformation Sequence | Stuttering | Congenital Adrenal Hyperplasia 1 | Hypertension | Esthesioneuroblastoma | Pierson Syndrome | Enterocolitis, Necrotizing | Atopy | Spinocerebellar Ataxia Type 6 | Jacobsen Syndrome | Restless Legs Syndrome | Scleritis | Vasculitis | Richter's Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Myofibromatosis | Hyperlipidemia