Disease

Androgen Insensitivity

About the Disease
Androgen Insensitivity Syndrome, also known as androgen resistance syndrome, is related to androgen insensitivity, partial and syndrome with 46,xy disorder of sex development. An important gene associated with Androgen Insensitivity Syndrome is AR (Androgen Receptor), and among its related pathways/superpathways are Signal Transduction and Metabolism of steroids. The drugs Miconazole and (R)-Bicalutamide have been mentioned in the context of this disorder. Affiliated tissues include testes, uterus and breast, and related phenotypes are delayed puberty and cryptorchidism

Common Targets
NR5A1 | G367 | HSD17B3

疾病靶点研报
Androgen Insensitivity

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

Other Diseases

Brachial Plexus Neuropathy | Multisystemic Smooth Muscle Dysfunction Syndrome | Hereditary Mixed Polyposis Syndrome | Coma | Anovulation | Familial Cerebral Amyloid Angiopathy | Zygomycosis | HELLP Syndrome | Trichotillomania | Angioedema, Acquired | Stuve-Wiedemann Syndrome | Craniolenticulosutural Dysplasia | Schindler Disease | Wolfram Syndrome 2 | Infectious Diarrhea | HANAC Syndrome | Rett Syndrome | Hyperinsulinemic Hypoglycemia | Pure Red Cell Aplasia | Autonomic Neuropathy | Antisocial Personality Disorder | Pemphigus | Meckel-Gruber Syndrome | Epilepsy, Generalized | Glycogen Storage Disease Type 1a | Cancer, Colon | HIBCH Deficiency | Huntington's Disease | Carcinoma, Merkel Cell | Waldenstrom Macroglobulinemia | Osteosclerosis | Early Infantile Epileptic Encephalopathy 28 | Erythromelalgia | Multiple Sclerosis | Hyperthermia, Malignant | Cluster Headache | Hyperglycemia | Bone Marrow Necrosis | MELAS Syndrome | Acute Coronary Syndrome | Hepatic Veno-occlusive Disease | Hyperkeratosis | Cutaneous T-cell Lymphoma | Ataxia-ocular Apraxia 2 | Chondrodysplasia Punctata 1, X-linked Recessive | Schizophrenia | Bare Lymphocyte Syndrome | Wilson's Disease | AIDS | Tylosis With Esophageal Cancer | Schuurs-Hoeijmakers Syndrome | Pontocerebellar Hypoplasia Type 2 | Amyloidosis | Brugada Syndrome 1 | Hepatitis, Alcoholic | Chronic Granulomatous Disease, X-linked | Hypertelorism | Pfeiffer Syndrome | Asperger Syndrome | Lyme Disease | Frontometaphyseal Dysplasia | Diffuse Intrinsic Pontine Glioma | Xeroderma Pigmentosum Variant Type | Systemic Lupus Erythematosus | Turner's Syndrome | Craniofacial Dysostosis | Muir-Torre Syndrome | Lymphoma Lymphoblastic | Osmotic Demyelination Syndrome | Basal Ganglia Disease | Epidermal Nevus Syndrome | Anti-NMDA Receptor Encephalitis | Asthma | Sleep Apnea, Obstructive | Beta-Propeller Protein-associated Neurodegeneration | Heterotaxy | Stiff-man Syndrome | Bronchitis | Erectile Dysfunction | Autonomic Nervous System Disorders | Incontinentia Pigmenti | Sialidosis Type I | McLeod Syndrome | Combined Malonic And Methylmalonic Acidemia | Thalassemia, Beta | Sleep Apnea, Central | Fibrosarcoma | Osteonecrosis | 3-methylcrotonyl-CoA Carboxylase Deficiency | Gastritis | Epidermolysis Bullosa Simplex | Renpenning Syndrome | Hemophagocytic Lymphohistiocytosis | Spinocerebellar Ataxia Type 15 | Dystonia | Tricho-hepato-enteric Syndrome | Ocular Hypertension | Ligneous Conjunctivitis | Ulcerative Colitis | Zollinger-Ellison Syndrome | Blepharitis | Spinocerebellar Ataxia | Subacute Sclerosing Panencephalitis | Iron Metabolism Disorders | Syphilis | Connective Tissue Disorders | Macrodactyly | Hepatitis A | Chitayat Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Autosomal Recessive Bestrophinopathy | Evans Syndrome | Knobloch Syndrome | Focal Segmental Glomerulosclerosis | Primary Hyperoxaluria Type 3 | Hypertension, Renal | Osteogenesis Imperfecta Type I | HUPRA Syndrome | Lamellar Ichthyosis | Adrenomyeloneuropathy | Multiple Congenital Anomalies-hypotonia-seizures Syndrome 2 | T-cell Prolymphocytic Leukemia | Juvenile Myoclonic Epilepsy | Generalized Epilepsy And Paroxysmal Dyskinesia | Paraganglioma, Carotid Body | Encephalitis | Hyperinsulinemia | Tyrosinemia Type 1 | Charcot-Marie-Tooth Disease, Type 6 | Colitis | Hyperparathyroidism, Primary | Carbohydrate Metabolism Disorders | Primary Familial Brain Calcification | Alazami Syndrome | Diverticulitis | Fucosidosis | Ganglioglioma | Mevalonate Kinase Deficiency | Autosomal Recessive Spastic Paraplegia Type 54 | Hyperparathyroidism, Secondary | Binge Eating Disorder | Vasculitis | Adenoma, Villous | Fukuyama Congenital Muscular Dystrophy | Cocaine-Related Disorders | Galactosialidosis | Duodenal Atresia | Otopalatodigital Syndrome Type 2 | Stickler Syndrome | Anthrax | Multiple Sclerosis, Secondary Progressive | Delayed Sleep Phase Syndrome | Jalili Syndrome | Coronary Artery Disease | Microtia | Holt-Oram Syndrome | Pycnodysostosis | Acromicric Dysplasia | Distal Myopathy | Cholangiocarcinoma | X-linked Creatine Transporter Deficiency | Hyperlipidemia Type V | Acral Lentiginous Melanoma | Hepatic Steatosis | Cantu Syndrome | Sarcoma | Glaucomatocyclitic Crisis | Neuroma | Hypermethioninemia | Oculocutaneous Albinism Type 4 | Antiphospholipid Syndrome | DiGeorge Syndrome | Anorchia | Medium-chain Acyl-CoA Dehydrogenase Deficiency | Crouzon Syndrome With Acanthosis Nigricans | Retinal Dystrophy, Early-onset Severe | Spondyloepiphyseal Dysplasia Tarda, X-linked | Nemaline Myopathy 8 | Hepatitis D | Dupuytren Disease | IMAGe Syndrome | Sarcosinemia | Glomerulonephritis, Membranoproliferative | 3-methylglutaconic Aciduria Type IV | Neuroblastoma | Toxoplasmosis | Coenzyme Q10 Deficiency | Myoclonus | Cervical Dystonia | Adenosine Deaminase Deficiency | Infantile Refsum Disease | Aspartylglycosaminuria | Corneal Dystrophies, Hereditary | Alagille Syndrome | Empyema | Hyperthyroidism | Niemann-Pick Disease | Alveolar Capillary Dysplasia | 3-M Syndrome | Dermatomyositis | Spondyloarthritis | Amyotrophic Lateral Sclerosis | Syncope | Glutaric Aciduria Type 3 | Dermatitis | Macular Degeneration | Multiple System Atrophy | Glucagonoma | Jacobsen Syndrome | Liebenberg Syndrome | Carcinoma, Signet Ring Cell | Bietti Crystalline Dystrophy | Kernicterus | Lysosomal Acid Lipase Deficiency | Sarcoma, Ewing | Tic Disorder | Renal Dysplasia | Teratozoospermia | Retinal Diseases | Chediak-Higashi Syndrome | Actinomycetoma | Leiomyosarcoma | Atrial Septal Defect | Persistent Hyperplastic Primary Vitreous | Congenital Mirror Movements | Primary Carnitine Deficiency | Heroin Dependence | Inflammatory Linear Verrucous Epidermal Nevus | Steel Syndrome | Intestinal Pseudo-obstruction | Myopia | Tendinopathy | Cystinosis | Retinitis | Angioedema | Endocarditis | Schnitzler Syndrome | Triphalangeal Thumb-polysyndactyly Syndrome | Robinow Syndrome | Williams Syndrome | Polycystic Kidney, Autosomal Recessive | Porphyria Cutanea Tarda | Multiple Sclerosis, Relapsing-remitting | Growth Hormone Excess | Urea Cycle Disorder | Wolcott-Rallison Syndrome | Congenital Stationary Night Blindness | Extramammary Paget's Disease | Mitochondrial Cytopathy | Facioscapulohumeral Muscular Dystrophy Type 1 | Early Infantile Epileptic Encephalopathy 4 | Pyoderma Gangrenosum | Aicardi-Goutieres Syndrome | Hemangioendothelioma | Granuloma Annulare | Myoclonic Epilepsy With Ragged Red Fibers | Chronic Lymphocytic Leukemia | Otitis Externa | Oligodendroglioma | Spondylocostal Dysostosis | Bronchiolitis | Microphthalmia | FG Syndrome | Marinesco-Sjogren Syndrome | Adenoma, Pleomorphic | Thrombocythemia, Essential | Rubeosis Iridis | Congenital Adrenal Hyperplasia 1 | Carbonic Anhydrase VA Deficiency | Trichomegaly | Frontotemporal Dementia With Amyotrophic Lateral Sclerosis | Oculocutaneous Albinism Type 1 | Peters-plus Syndrome | Trigonocephaly | Neutrophilia | Amebiasis | Okihiro Syndrome | Hereditary Xerocytosis | Abetalipoproteinemia | Bicuspid Aortic Valve | Trichuriasis | Histiocytic Sarcoma | Progressive Familial Intrahepatic Cholestasis | Neuropathy | Galactosemia | Porphyria, Acute Intermittent | Progressive Osseous Heteroplasia | Schistosomiasis Mansoni | Exostoses | Pierpont Syndrome | Waardenburg Syndrome Type 4A | Leukodystrophies | Cancer, Lung | Vitamin A Deficiency | Usher Syndrome Type IIC | Nephritis, Interstitial | Autosomal Recessive Congenital Ichthyosis | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Cholecystitis | Leishmaniasis, Cutaneous | Hemorrhage | Hypohidrotic Ectodermal Dysplasia, X-linked | Ebstein Anomaly | Gingivitis | Multicystic Renal Dysplasia | Hepatitis, Chronic | Pterygium | Crigler-Najjar Syndrome | Sclerosing Cholangitis | Encephalopathy, Hepatic | Pseudohermaphroditism | DOCK8 Immunodeficiency Syndrome | Duane Retraction Syndrome | Veno-occlusive Disease | Esophageal Motility Disorders | Histiocytosis | Angiosarcoma | Arthritis, Reactive | Giant Axonal Neuropathy | Treacher Collins Syndrome | Hypertriglyceridemia | Chronic Thromboembolic Pulmonary Hypertension | Fahr Disease | Cramp Fasciculation Syndrome | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Rash | Lewy Body Dementia | Guillain-Barre Syndrome | Cholesteryl Ester Storage Disease | Cenani-Lenz Syndactyly Syndrome | Colitis, Microscopic | Gastrointestinal Disorders | Blepharo-cheilo-odontic Syndrome | Cholangitis | Pityriasis Rubra Pilaris | Renal Tubular Dysgenesis | Dermatofibrosarcoma | Renal Hypouricemia | Temporal Lobe Epilepsy | 3-hydroxy-3-methylglutaric Aciduria | Corticobasal Syndrome | Hemochromatosis Type 1 | Malignant Peripheral Nerve Sheath Tumor | Antenatal Bartter Syndrome Type 1 | Osteoporosis, Postmenopausal | T-cell Leukemia | Blue Rubber Bleb Nevus Syndrome | Sweet Syndrome | Cavitary Optic Disc Anomalies | Apparent Mineralocorticoid Excess Syndrome | Neurofibromatosis Type 2 | Proteus Syndrome | Coffin-Lowry Syndrome | Renal Medullary Carcinoma | Corneal Dystrophy And Perceptive Deafness | Melanoma | VEXAS Syndrome | Porokeratosis | Occipital Neuralgia | Optic Neuritis | ACTH-independent Macronodular Adrenal Hyperplasia | Spinocerebellar Ataxia Type 17 | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Pierre Robin Syndrome | Monilethrix | Fabry's Disease | MIRAGE Syndrome | Rhinitis | Ectopia Lentis, Isolated, Autosomal Recessive | Polycythemia Vera | Glycogen Storage Disease Type 3 | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Ellis-Van Creveld Syndrome | Zimmermann-Laband Syndrome | Hepatitis B, Chronic | Fibronectin Glomerulopathy | Biotinidase Deficiency | Persistent Truncus Arteriosus | Charcot-Marie-Tooth Disease | Brachydactyly | Ichthyosis Bullosa Of Siemens | Mitochondrial Myopathy | Tremor | Oculopharyngeal Muscular Dystrophy | Viral Meningitis | ADNP Syndrome | Hodgkin Lymphoma | Pilomatrix Carcinoma | Retinopathy, Diabetic | Arteriosclerosis | Autoimmune Polyendocrinopathy Syndrome Type I | Amelanotic Melanoma | Neurotoxicity | Chondrodysplasia Punctata 2, X-linked Dominant | Sarcoidosis, Pulmonary | Congenital Nystagmus | Familial Hemiplegic Migraine | Cutis Laxa | Ganglioneuroma | Myasthenia Gravis