Disease

Autoimmune Polyendocrine Syndrome

About the Disease
Autoimmune Polyendocrine Syndrome, also known as autoimmune polyglandular failure, is related to autoimmune polyendocrine syndrome, type ii and autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia. An important gene associated with Autoimmune Polyendocrine Syndrome is AIRE (Autoimmune Regulator), and among its related pathways/superpathways are Innate Immune System and Immune response IL-23 signaling pathway. The drugs Hydroxyurea and Racepinephrine have been mentioned in the context of this disorder. Affiliated tissues include thyroid, t cells and thymus, and related phenotypes are homeostasis/metabolism and immune system

Common Targets
FOXD3 | HLA-A | G7124 | CTLA4 | VDR | PTPN22

疾病靶点研报
Autoimmune Polyendocrine Syndrome

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

Other Diseases

Tracheal Disorders | Specific Granule Deficiency | Meningioma, Benign | Parvovirus B19 Infection | Protein S Deficiency | Craniopharyngioma | Sponastrime Dysplasia | Liver Failure, Acute Infantile | Cardiac Arrest | Endophthalmitis | Necrobiosis Lipoidica | Pontocerebellar Hypoplasia Type 2 | Ornithine Transcarbamylase Deficiency | Acrodermatitis Enteropathica | Congenital Ichthyosiform Erythroderma | Progressive Osseous Heteroplasia | Gnathodiaphyseal Dysplasia | Dowling-Degos Disease | Optic Neuritis | Cataplexy | Hyperbilirubinemia, Neonatal | Perivascular Epithelioid Cell Tumor | Connective Tissue Disorders | Schizophrenia, Paranoid | Epidermolysis Bullosa Simplex, Generalized | Hamartoma | Empyema | Melanoma, Malignant | Sandhoff Disease | Blastomycosis | Thrombotic Microangiopathy | Meier-Gorlin Syndrome | Hyperlipidemia, Familial Combined | X-linked Acrogigantism | Camurati-Engelmann Disease | Intestinal Hypomagnesemia 1 | Sickle Cell Anemia | Cerebrotendinous Xanthomatosis | Congenital Stromal Corneal Dystrophy | Spondyloepiphyseal Dysplasia Tarda, X-linked | Lathosterolosis | Benign Familial Pemphigus | Myocardial Infarction | Peters-plus Syndrome | Enterocolitis, Necrotizing | Torticollis | Meckel-Gruber Syndrome | Gout | Colitis, Microscopic | Bartsocas-Papas Syndrome | Mesothelioma, Malignant | Agoraphobia | Duodenal Atresia | Syndactyly | Multifocal Motor Neuropathy | Bernard-Soulier Syndrome | Pseudohypoaldosteronism | Toxic Epidermal Necrolysis | Prediabetes | Autosomal Recessive Congenital Ichthyosis | Lichen Sclerosus | Galactosialidosis | Hyperinsulinism-hyperammonemia Syndrome | Low Phospholipid Associated Cholelithiasis | Charcot-Marie-Tooth Disease, Type 1A | Hartsfield Syndrome | Glioma | Fetal Alcohol Syndrome | Bronchitis | Congenital Lipoid Adrenal Hyperplasia | Spinal Muscular Atrophy | Hidradenitis Suppurativa | Chronic Myelomonocytic Leukemia | Hyperoxaluria | Corticobasal Syndrome | Zellweger Syndrome | Ureteropelvic Junction Obstruction | Geleophysic Dysplasia | Acute Coronary Syndrome | Reticular Dysgenesis | Diabetic Macular Edema | Chiari Malformation Type I | Hemochromatosis | Axenfeld-Rieger Syndrome | Plasma Cell Leukemia | Barrett Esophagus | Chronic Lymphocytic Leukemia | Achondrogenesis | Blue Rubber Bleb Nevus Syndrome | Diffuse Intrinsic Pontine Glioma | Cryopyrin-associated Periodic Syndromes | Glaucoma | Polycythemia | Growth Hormone Excess | Rhizomelic Chondrodysplasia Punctata | Basal Cell Nevus Syndrome | Pulmonary Capillary Hemangiomatosis | Ollier Disease | Echinococcosis | Macrophagic Myofasciitis | Diarrhea | Seborrheic Dermatitis | Thalassemia | Aneurysm, Abdominal Aortic | Optic Neuropathy | Tyrosine Hydroxylase Deficiency | Mycosis Fungoides | Epithelial-myoepithelial Carcinoma | Central Core Disease | Maternally Inherited Diabetes And Deafness | Metatropic Dysplasia | Eosinophilic Asthma | Epidermodysplasia Verruciformis | Hydrolethalus Syndrome | Aneurysm, Thoracic Aortic | Intellectual Disability, Autosomal Dominant 5 | Infantile Neuroaxonal Dystrophy | Nephropathy | Stevens-Johnson Syndrome | Diabetes Mellitus, Transient Neonatal | Porphyria, Variegate | Hyperinsulinemic Hypoglycemia | Mucolipidosis | Pouchitis | Netherton Syndrome | Duchenne Muscular Dystrophy | Aldosterone Deficiency | Galactosemia | Brugada Syndrome 1 | C3 Glomerulonephritis | Reye Syndrome | Retinitis | Blastoma, Pleuropulmonary | Myoclonic Epilepsy With Ragged Red Fibers | Keratitis-ichthyosis-deafness Syndrome | Trachoma | Aromatic L-amino Acid Decarboxylase Deficiency | Binge Eating Disorder | POEMS Syndrome | Malignant Peripheral Nerve Sheath Tumor | Muir-Torre Syndrome | Leukoencephalopathy, Progressive Multifocal | Charcot-Marie-Tooth Disease, Type 2A | Sarcoidosis, Pulmonary | Autosomal Recessive Spastic Paraplegia Type 75 | Anorectal Malformations | Uremia | Glomerulonephritis, Membranoproliferative | Crouzon Syndrome With Acanthosis Nigricans | Nicotine Addiction | Imerslund-Grasbeck Syndrome | Hyperferritinemia-cataract Syndrome | Hypoglycemia | Hypersensitivity | Spinocerebellar Ataxia Type 17 | Huntington's Disease | Primary Erythromelalgia | IgA Nephropathy | KBG Syndrome | Cholecystitis | Chylothorax, Congenital | Lymphoproliferative Disorders | Osteochondrosis | Infertility, Male | Porokeratosis | Neurofibroma, Plexiform | Delayed Sleep Phase Syndrome | Nemaline Myopathy | Neurofibroma | Paraplegia | CHOPS Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Duane Retraction Syndrome | Adenocarcinoma | Hyperthyroidism | Arteriosclerosis | Granular Corneal Dystrophy | Kallmann Syndrome | Nicolaides-Baraitser Syndrome | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | Short-chain Acyl-CoA Dehydrogenase Deficiency | Polycystic Kidney, Autosomal Dominant | Synpolydactyly | Congenital Nystagmus | Chromosome 5q Deletion Syndrome | Spinocerebellar Ataxia Type 14 | Myelofibrosis | Idiopathic Multicentric Castleman Disease | NDH Syndrome | Coma | Hereditary Sensory And Autonomic Neuropathy | Facioscapulohumeral Muscular Dystrophy Type 2 | Hereditary Elliptocytosis | Spermatocele | Spinocerebellar Ataxia Type 5 | Avellino Corneal Dystrophy | Hemophagocytic Lymphohistiocytosis | Blood Protein Disorders | Heart Septal Defects | Amyotrophic Lateral Sclerosis | Tinea Versicolor | TARP Syndrome | Lipodystrophy | Nager Acrofacial Dysostosis | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Alexander Disease | Vascular Cognitive Impairment | Desbuquois Syndrome | Myasthenia | Fowler's Syndrome | Thanatophoric Dysplasia | Okihiro Syndrome | Ligneous Conjunctivitis | Epilepsy | Familial Exudative Vitreoretinopathy | Cranial Nerve Disease | Spinocerebellar Ataxia Type 10 | Gaze Palsy, Familial Horizontal, With Progressive Scoliosis, 2 | Non-proliferative Diabetic Retinopathy | Insulin Resistance | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 2 | Succinic Semialdehyde Dehydrogenase Deficiency | GNE Myopathy | Congenital Nephrotic Syndrome | Dengue Hemorrhagic Fever | Dyggve-Melchior-Clausen Disease | Lymphoproliferative Disease, X-linked | Glomerulonephritis, Membranous | Glycogen Storage Disease Type 1a | Platyspondylic Lethal Skeletal Dysplasia, Torrance Type | Adenosine Deaminase 2 Deficiency | Schizoaffective Disorder | Fibrodysplasia Ossificans Progressiva | Chorioretinitis | Polyomavirus Nephropathy | Rotor Syndrome | Waardenburg Syndrome Type 1 | Ganglioneuroma | Patent Foramen Ovale | Liver Failure | Nevus | Goiter | Generalized Epilepsy And Paroxysmal Dyskinesia | Atrioventricular Septal Defect | Nutrition Disorders | Granular Corneal Dystrophy Type 1 | Cranioectodermal Dysplasia | Leukemia | Epilepsy, Generalized | Chronic Thromboembolic Pulmonary Hypertension | Oral Lichen Planus | Spinocerebellar Ataxia Type 21 | Thin Basement Membrane Disease | Arterial Tortuosity Syndrome | Homocystinuria | Mixed Connective Tissue Disease | Hereditary Spherocytosis | Disseminated Intravascular Coagulation | Basal Ganglia Disease | Tendinopathy | Fibrosarcoma | HIBCH Deficiency | Klippel-Feil Syndrome | Spinal Cord Diseases | Celiac Disease | Choroiditis | Sengers Syndrome | Tic Disorder | Alpers Syndrome | Silver-Russell Syndrome | Tularemia | Retinitis Pigmentosa | Chondrodysplasia Punctata 2, X-linked Dominant | Pyruvate Decarboxylase Deficiency | Prostatitis | Premature Ejaculation | Retinal Coloboma | Sarcoma, Alveolar Soft Part | Fragile X Syndrome | Corneal Dystrophies, Hereditary | Pulmonary Stenosis | Dysequilibrium Syndrome | Graves Disease | Trichothiodystrophy | Epilepsy Of Infancy With Migrating Focal Seizures | Wolff-Parkinson-White Syndrome | Spondylocostal Dysostosis | Incontinentia Pigmenti | Spinocerebellar Ataxia Type 20 | Intestinal Obstruction | Gray Platelet Syndrome | Sleep Disorder | Retinal Telangiectasia | Hemangioblastoma | Familial Digital Arthropathy-brachydactyly | Cholangitis | Poikiloderma With Neutropenia | Amblyopia | Adrenal Insufficiency | Hepatitis E | Obesity | Niemann-Pick Disease, Type C | Trichomegaly | Nephronophthisis | Retinopathy, Diabetic | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Pseudohypoparathyroidism Type 1B | Acute Anterior Uveitis | Aspergillosis | Esophageal Carcinoma | Tonsillitis | Osmotic Demyelination Syndrome | Pancreatitis, Chronic | Schwannoma | Sturge-Weber Syndrome | Hypopituitarism | Spinocerebellar Ataxia | Asthma, Nocturnal | Osteopathia Striata With Cranial Sclerosis | Open-angle Glaucoma | Isovaleric Acidemia | Combined Deficiency Of Factor V And Factor VIII | Hypertension, Pulmonary | Kaposiform Hemangioendothelioma | Congenital Aniridia | Sitosterolemia | Vici Syndrome | Cartilage Disorders | Whipple's Disease | Melanoma, Uveal | Castleman Disease | Epiphyseal Chondrodysplasia, Miura Type | Congenital Dyserythropoietic Anemia | Varices | Congenital Bilateral Absence Of Vas Deferens | Chronic Beryllium Disease | Larsen Syndrome | CHARGE Syndrome | Wolfram Syndrome 2 | Anterior Segment Dysgenesis | Hypermetropia | Myopia | Creatine Deficiency Syndrome Due To AGAT Deficiency | Blepharo-cheilo-odontic Syndrome | Papulopustular Rosacea | Craniofrontonasal Syndrome | Dermatitis Herpetiformis | Hemochromatosis Type 2 | Charcot-Marie-Tooth Disease Axonal Type 2N | Allergic Contact Dermatitis | 3-methylglutaconic Aciduria | Gangliosidosis | Chronic Myeloid Leukemia | Lymphangioma | Congenital Absence Of Vas Deferens | Genitopatellar Syndrome | Neutrophilia | Majeed Syndrome | Autosomal Recessive Spastic Paraplegia Type 35 | Charcot-Marie-Tooth Disease Type 4D | Gilbert Syndrome | Leukoplakia | Mitochondrial Cytopathy | Familial Cerebral Amyloid Angiopathy | Triple A Syndrome | Allan-Herndon-Dudley Syndrome | Spinocerebellar Ataxia Type 13 | Metabolic Diseases | Christianson Syndrome | GAPO Syndrome | Thrombocytopenia | Canavan Disease | Smith-Kingsmore Syndrome | Rift Valley Fever | Astigmatism | Optic Atrophy 2 | Glutaric Aciduria Type 2 | Herpes Genitalis | Subcortical Band Heterotopia | Androgenic Alopecia | Progressive External Ophthalmoplegia | Spinocerebellar Ataxia Type 28 | Primary Lateral Sclerosis | Nephrotic Syndrome Type 1 | Pseudohermaphroditism | Arthritis, Reactive | Panic Disorder | Pigment Dispersion Syndrome | Liddle Syndrome | Loeys-Dietz Syndrome | Long QT Syndrome Type 3 | Schuurs-Hoeijmakers Syndrome | REM Sleep Behavior Disorder | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Pneumothorax | Metaphyseal Chondrodysplasia, Schmid Type | Iron Metabolism Disorders | Cutaneous T-cell Lymphoma | Long-chain 3-hydroxyacyl-coenzyme A Dehydrogenase Deficiency | Uterine Leiomyoma