Disease

Alopecia Areata

About the Disease
Alopecia Areata, also known as alopecia circumscripta, is related to alopecia universalis congenita and alopecia, and has symptoms including exanthema and pruritus. An important gene associated with Alopecia Areata is AA1 (Alopecia Areata 1), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. The drugs Cetirizine and Histamine have been mentioned in the context of this disorder. Affiliated tissues include skin, breast and t cells, and related phenotypes are Synthetic lethal with MLN4924 (a NAE inhibitor) and Synthetic lethal with MLN4924 (a NAE inhibitor)

Common Targets
ANKRD12 | PTPN2 | Interleukin 17 (nonspecified subtype) | IL-15 receptor | CDK6 | LINC00824 | ADAMTS6 | Phosphodiesterase IV (PDE4) (nonspecified subtype) | IL2RA | IL17RA | TYK2 | G1950 | HLA-B | NPC1L1 | ERBB3 | BCR | DHODH | CAMTA1 | HLA-DRB1 | HMGCR | MC2R | PRORP | BTNL2 | CD86 | SPATA5 | Liver Bile Transporters (LBAT) (nonspecified subtype) | IL-2 receptor | Neurotrophic Factor (nonspecified subtype) | PDIA6 | IL-4 receptor | SOD2 | GPX1 | HLA-A | G3605 | KLRK1 | IL15 | G7124 | XKR6 | GSTT1 | LILRA4 | ACHE | GZMB | CES1 | EZH1 | Mitogen-Activated Protein Kinase (nonspecified subtype) | BLTP1 | G4233 | TRIM71 | SLC10A1 | CTLA4 | VDR | IL17F | KLRC4-KLRK1 | ACOXL | CPD | CHIA | CD80 | FASLG | LINC01934 | KDR | RET | KRT82 | TXNRD1 | Janus Kinase (nonspecified subtype) | PTPN22 | IL16 | CLEC16A | G1956 | TLR9 | IFNG | FAS | Histone deacetylase (nonspecified subtype) | GSTM1 | GSTP1 | SFRP1 | MIF | STX17 | Retinoid RXR receptor (nonspecified subtype) | SPOCK1 | IL4 | HLA-DRB5 | JAK3 | JAK1 | Mitogen-activated protein kinase (JNK) (nonspecified subtype) | MICA | TEAD1 | HLA-C | ABL1 | IL13 | JAK2 | IL23R | ATXN2 | HLA-DQB1 | IL9R | NFKB1 | RASAL2 | G5133 | Phosphodiesterase (nonspecified subtype) | IL12B | KIT | RORC | ACTA2

疾病靶点研报
Alopecia Areata

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

Other Diseases

Hepatopulmonary Syndrome | Priapism | Delayed Sleep Phase Syndrome | Arteriovenous Malformations | Congenital Adrenal Hyperplasia 1 | Placenta Previa | Neurofibrosarcoma | Hemoglobinopathies | Spinocerebellar Ataxia Type 21 | Leukocyte Adhesion Deficiency | Tangier Disease | Malonyl-CoA Decarboxylase Deficiency | Ichthyosis Bullosa Of Siemens | Lymphangioma | Bullous Pemphigoid | Krabbe Disease | Vitelliform Macular Dystrophy | Basal Cell Nevus Syndrome | Choroideremia | Otopalatodigital Syndrome Type 2 | Non-small Cell Lung Cancer | Alzheimer Disease, Late Onset | Periventricular Nodular Heterotopia | Stroke | Sleep Disorder | Pseudo-pseudohypoparathyroidism | Bietti Crystalline Dystrophy | Glutaric Aciduria Type 2 | Pseudohypoparathyroidism Type 1B | Hemorrhage | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Learning Disability | Sclerosteosis | Gastrointestinal Disorders | Poretti-Boltshauser Syndrome | Tonsillitis | Chronic Neutrophilic Leukemia | Angelman Syndrome | Hypopigmentation | Acromicric Dysplasia | Brugada Syndrome 1 | Early Infantile Epileptic Encephalopathy 28 | Congenital Tufting Enteropathy | Analgesia | Kernicterus | Myopathy | Schwartz-Jampel-Aberfeld Syndrome | Chronic Enteropathy Associated With SLCO2A1 Gene | Gangliosidosis, GM1 | Cataract | Early Infantile Epileptic Encephalopathy 4 | AIDS Dementia Complex | Hyperostosis | Thalassemia, Beta | Sialidosis Type I | Emery-Dreifuss Muscular Dystrophy | Hepatic Steatosis | Familial Isolated Hyperparathyroidism | Pneumothorax | Isovaleric Acidemia | Hyperglycemia | Fibromuscular Dysplasia | Nephrocalcinosis | Zimmermann-Laband Syndrome | Anovulation | Whipple's Disease | Allan-Herndon-Dudley Syndrome | Diamond-Blackfan Anemia | Neurofibromatosis Type 2 | Usher Syndrome Type I | Primary Aldosteronism | Pemphigoid | Multicystic Renal Dysplasia | Osteogenesis Imperfecta Type III | Lyme Disease | Aneurysm, Thoracic Aortic | Cluster Headache | Low Phospholipid Associated Cholelithiasis | Peters-plus Syndrome | Axenfeld-Rieger Syndrome | Progressive Familial Intrahepatic Cholestasis Type 1 | Gastritis, Atrophic | Ataxia-ocular Apraxia 2 | Glycogen Storage Disease Type 1a | Vitiligo | Autoimmune Disease | Uremic Pruritus | Takenouchi-Kosaki Syndrome | Infantile Refsum Disease | 3-M Syndrome | Familial Episodic Pain Syndrome | Diffuse Intrinsic Pontine Glioma | Chordoid Glioma | Erythropoietic Protoporphyria | Arterial Tortuosity Syndrome | Dubin-Johnson Syndrome | Endocarditis | Pain | Pupil Disorders | Carbonic Anhydrase VA Deficiency | GNE Myopathy | Rett Syndrome | Gray Platelet Syndrome | Ellis-Van Creveld Syndrome | Conjunctivitis, Allergic | Sturge-Weber Syndrome | Skin Papilloma | Psoriasis | Pseudoexfoliation Syndrome | Epilepsy Of Infancy With Migrating Focal Seizures | Gardner Syndrome | Metaphyseal Chondrodysplasia, Schmid Type | Phosphoglycerate Dehydrogenase Deficiency | Irritable Bowel Syndrome | Periodontitis | Stuve-Wiedemann Syndrome | Periodic Limb Movement Disorder | Crouzon Syndrome With Acanthosis Nigricans | Papillon-Lefevre Syndrome | Wiskott-Aldrich Syndrome | Melnick-Needles Syndrome | Multiple Sclerosis, Primary Progressive | Cranioectodermal Dysplasia | GM2-gangliosidosis AB Variant | Adams-Oliver Syndrome | Still Disease | Cryptorchidism | Pseudohypoparathyroidism Type 1A | Dysthymia | Keratoconjunctivitis | HELLP Syndrome | Astigmatism | Obsessive-compulsive Disorder | Micropenis | Ghosal Syndrome | Osteochondroma | Thrombocytopenia | Acute Motor Axonal Neuropathy | Keratoacanthoma | Microphthalmia | Proopiomelanocortin Deficiency | Hypolipoproteinemia | Shprintzen-Goldberg Syndrome | Prune Belly Syndrome | Transthyretin-related Amyloidosis | Nephrosclerosis | Chondromyxoid Fibroma | Spondylometaphyseal Dysplasia | Autoimmune Polyendocrine Syndrome | Blepharo-cheilo-odontic Syndrome | LEOPARD Syndrome | Metachondromatosis | Hyperprolactinemia | Pouchitis | Neutropenia | Galloway-Mowat Syndrome | Iron Deficiency Anemia | Cancer, Prostate | Keratosis, Seborrheic | Osteoarthritis | Tibial Muscular Dystrophy | Lymphangiomatosis | Pregnancy, Ectopic | Pemphigus | CHOPS Syndrome | Maternally Inherited Diabetes And Deafness | Migraine | Kaposiform Hemangioendothelioma | Cheilitis | Ureteropelvic Junction Obstruction | Herpes Simplex Dermatitis | Glomerulonephritis, Membranoproliferative | Hepatic Veno-occlusive Disease | Intracranial Hypertension | Lymphoma, Follicular | Schwannomatosis | Retinopathy Of Prematurity | Hyperthyroidism | Carcinoma, Signet Ring Cell | Carpal Tunnel Syndrome | Asthma | Homocystinuria | Malnutrition | Acute Lung Injury | Nemaline Myopathy 10 | Presbyopia | Pendred Syndrome | Japanese Encephalitis | Conjunctivitis | Preaxial Polydactyly | Retinal Degeneration | Hereditary Xerocytosis | Glioblastoma Multiforme | Acute Leukemia | Bone Giant Cell Tumor | Pyoderma Gangrenosum | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Celiac Disease | Meleda Disease | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Liver Diseases | Vertebrobasilar Insufficiency | Currarino Syndrome | Peroxisomal Disorder | Erythematotelangiectatic Rosacea | Mandibuloacral Dysplasia With Type A Lipodystrophy | Keratocystic Odontogenic Tumor | Primary Lateral Sclerosis | Chylomicron Retention Disease | Toxic Epidermal Necrolysis | MIRAGE Syndrome | Oculocutaneous Albinism Type 1 | Tinea Versicolor | Traboulsi Syndrome | Pterygium | Gastroschisis | Seminoma | Aplasia Cutis Congenita | Apert Syndrome | Alpha-thalassemia Myelodysplasia Syndrome | Zollinger-Ellison Syndrome | Schnitzler Syndrome | Scabies | X-linked Charcot-Marie-Tooth Disease | Sensorineural Hearing Loss | Saethre-Chotzen Syndrome | Polycystic Liver | Premenstrual Syndrome | Hydronephrosis | Paroxysmal Nocturnal Hemoglobinuria | Cholangiocarcinoma | Spinocerebellar Ataxia Type 12 | Von Willebrand Disease | Pyelonephritis | Pituitary Disorders | Lupus Erythematosus | Light Chain Amyloidosis | Hamartoma | Glanzmann Thrombasthenia | Brenner Tumor | Hereditary Sensory And Autonomic Neuropathy | Infantile Spasm | Wolfram Syndrome 2 | Hyperinsulinism-hyperammonemia Syndrome | Progressive Encephalopathy-optic Atrophy Syndrome | Membranous Nephropathy | Hyperinsulinemia | Hyperferritinemia-cataract Syndrome | Multiple Sclerosis | Microcephalic Osteodysplastic Primordial Dwarfism, Type I | Spondylolisthesis | CDKL5 Deficiency Disorder | Charcot-Marie-Tooth Disease Type 3 | Liver Failure, Acute Infantile | Pyruvate Carboxylase Deficiency Disease | Tietze Syndrome | Disseminated Superficial Actinic Porokeratosis | Diabetes Type 1 | Anodontia | Mosaic Variegated Aneuploidy Syndrome 2 | Spinocerebellar Ataxia Type 10 | PASLI Disease | Neurofibromatosis-Noonan Syndrome | Diabetes Insipidus, Neurogenic | Desbuquois Syndrome | Hypertensive Retinopathy | Familial Dysautonomia | Sarcoma, Endometrial Stromal | Sporadic Hemiplegic Migraine | Retinal Telangiectasia | Cardiac Sarcoidosis | Chronic Granulomatous Disease, X-linked | Hypotension, Orthostatic | Carpenter Syndrome | Megalencephaly | Oligospermia | McLeod Syndrome | Papulopustular Rosacea | Lysosomal Acid Lipase Deficiency | Lactose Intolerance | Congenital Myopathy | Cancer, Bladder | Pachyonychia Congenita | Ichthyosis | Congenital Hereditary Endothelial Dystrophy Type II | Centronuclear Myopathy | Impetigo | REM Sleep Behavior Disorder | Carney Triad | PHARC Syndrome | DOCK8 Immunodeficiency Syndrome | Dermatitis | Myofibrillar Myopathy | Cutis Laxa | Chromosome 16p11.2 Deletion Syndrome | Von Hippel-Lindau Disease | Juvenile Polyposis | Eosinophilic Asthma | Aromatic L-amino Acid Decarboxylase Deficiency | Glycogen Storage Disease Type 6 | Hypertension, Pulmonary | Nager Acrofacial Dysostosis | Kaposi Sarcoma | Paraplegia | Cat Eye Syndrome | Waardenburg Syndrome | Autonomic Nervous System Disorders | Amyotrophic Lateral Sclerosis | Hypertriglyceridemia | Blepharoconjunctivitis | Pseudomyxoma Peritonei | Hypodontia | Early Infantile Epileptic Encephalopathy | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Left Ventricular Noncompaction | Hereditary Elliptocytosis | Hypotrichosis Simplex | Encephalopathy, Ethylmalonic | Wolman Disease | Multiple Sclerosis, Secondary Progressive | Creatine Deficiency Syndrome | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Cystitis, Interstitial | Pulmonary Vein Stenosis | Schistosomiasis | Schnyder Crystalline Corneal Dystrophy | Craniofrontonasal Syndrome | Citrullinemia | Imerslund-Grasbeck Syndrome | Glycogen Storage Disease Type 5 | Overactive Bladder | Lennox-Gastaut Syndrome | Exotropia | Chromosome 9q34.3 Deletion Syndrome | Osteoglophonic Dysplasia | Microcephalic Osteodysplastic Primordial Dwarfism, Type II | Nephrotic Syndrome Type 1 | Epidermolysis Bullosa | Charcot-Marie-Tooth Disease | Thrombotic Microangiopathy | Cerebellar Ataxia, Cayman Type | Dyskeratosis Congenita | Asphyxia Neonatorum | Waardenburg Syndrome Type 1 | Retinal Dystrophy | Glutathione Synthetase Deficiency | Narcolepsy | Congenital Mirror Movements | Papillorenal Syndrome | Charcot-Marie-Tooth Disease Type 2D | Osteosclerosis | Hypohidrotic Ectodermal Dysplasia | Pilomatrix Carcinoma | Zellweger Syndrome | Avian Influenza | Juvenile Hyaline Fibromatosis | Majeed Syndrome | Low Tension Glaucoma | Ollier Disease | Hyperoxaluria | Astrocytoma, Anaplastic | Keratoconus | Pituitary Stalk Interruption Syndrome | Pneumonia, Viral | HIBCH Deficiency | Ventricular Septal Defect | Pancreatitis, Chronic | Becker Muscular Dystrophy | Chondrodysplasia Punctata 1, X-linked Recessive | Spinocerebellar Ataxia Type 6 | Non-bullous Congenital Ichthyosiform Erythroderma | Tuberculosis | Blue Nevus | Erythema Multiforme | Greig Cephalopolysyndactyly Syndrome | HANAC Syndrome | Focal Cortical Dysplasia Type 2 | Amelanotic Melanoma | Myoclonus-dystonia Syndrome | Blepharitis | Hyperparathyroidism, Primary | Hyperthermia, Malignant | Open-angle Glaucoma | Branchiootorenal Syndrome | Pyloric Stenosis, Infantile Hypertrophic | Craniofacial Dysostosis | Van Der Knaap Disease | Multicentric Carpotarsal Osteolysis Syndrome | Hypertensive Nephropathy | Duchenne Muscular Dystrophy | Oculocutaneous Albinism Type 2 | Sialidosis | Jaundice, Obstructive | Chronic Inflammatory Demyelinating Polyneuropathy | Blepharospasm | Melanoma, Malignant | Cramp Fasciculation Syndrome | Charcot-Marie-Tooth Disease Type 4B1 | Major Depression | Cystinosis