Disease

Alopecia Totalis

About the Disease
Alopecia Totalis, also known as loss of all scalp hair, is related to alopecia areata and woodhouse-sakati syndrome. An important gene associated with Alopecia Totalis is UQCRFS1 (Ubiquinol-Cytochrome C Reductase, Rieske Iron-Sulfur Polypeptide 1). The drugs Hydroxychloroquine and Orange have been mentioned in the context of this disorder. Affiliated tissues include skin, thyroid and nk cells, and related phenotypes are alopecia of scalp and alopecia

Common Targets
JAK3 | JAK1

疾病靶点研报
Alopecia Totalis

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

Other Diseases

Spinocerebellar Ataxia Type 42 | Corticobasal Syndrome | Farber Disease | Chanarin-Dorfman Syndrome | Pendred Syndrome | GM2-gangliosidosis AB Variant | Arthritis | Proopiomelanocortin Deficiency | Zollinger-Ellison Syndrome | Rett Syndrome | Asplenia | Lafora Disease | Myoclonic Atonic Epilepsy | Dementia | Peters-plus Syndrome | Muckle-Wells Syndrome | Giant Cell Arteritis | Ectodermal Dysplasia | 3C Syndrome | Carcinoid Tumor | Overactive Bladder | Takotsubo Cardiomyopathy | Androgen Insensitivity | Neurodevelopmental Disorder With Central Hypotonia And Dysmorphic Facies | Sarcosinemia | Christianson Syndrome | CDKL5 Deficiency Disorder | Neurofibromatosis Type 2 | Meningioma, Benign | Bulimia Nervosa | Glomerulonephritis, Membranous | Thromboembolism | Glycogen Storage Disease Type 0 | Lymphedema | POEMS Syndrome | Epiphyseal Chondrodysplasia, Miura Type | Dementia, Vascular | C3 Glomerulopathy | Pulmonary Capillary Hemangiomatosis | Hypogonadism | Progressive Familial Intrahepatic Cholestasis Type 2 | Myocardial Infarction | Microcephaly | Synpolydactyly | Babesiosis | Pouchitis | Spinocerebellar Ataxia Type 31 | B-cell Prolymphocytic Leukemia | Kleine-Levin Syndrome | Renal Tubular Acidosis | Hyperparathyroidism | Carey-Fineman-Ziter Syndrome | Adenomatoid Tumor | Tenosynovial Giant Cell Tumor | Thrombasthenia | Spondylocarpotarsal Synostosis Syndrome | Familial Partial Lipodystrophy | Osteomyelitis | Camptocormia | Hereditary Inclusion Body Myopathy | Salla Disease | Eating Disorder | Cardiomyopathy, Hypertrophic | Sick Sinus Syndrome 1 | Crimean-Congo Hemorrhagic Fever | Speech Disorders | Seizures | Insulin Resistance | Scleroderma, Diffuse | PHARC Syndrome | Seizures-scoliosis-macrocephaly Syndrome | Necrotizing Autoimmune Myopathy | Liebenberg Syndrome | Glomerulonephritis | Neurotoxicity | Sulfite Oxidase Deficiency | Metachondromatosis | Leukoencephalopathy, Progressive Multifocal | Coma | Schuurs-Hoeijmakers Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Impulse Control Disorder | Neural Tube Defect | Stickler Syndrome | Congenital Nephrotic Syndrome | Rhizomelic Chondrodysplasia Punctata | Hereditary Spherocytosis | Thrombophlebitis | Metabolic Syndrome | Epilepsy | Congenital Muscular Dystrophy | Glycogen Storage Disease Type 5 | Sporadic Hemiplegic Migraine | Gnathodiaphyseal Dysplasia | Arts Syndrome | Combined Deficiency Of Factor V And Factor VIII | Ectopia Lentis, Isolated, Autosomal Recessive | Angelman Syndrome | Cyclic Vomiting Syndrome | Membranous Nephropathy | Anorectal Malformations | Gallstones | Thymoma, Malignant | Alstrom Syndrome | Heavy Chain Disease | Periodic Limb Movement Disorder | Ureteropelvic Junction Obstruction | Gastroschisis | Smith-Lemli-Opitz Syndrome | NGLY1 Deficiency | Cryptosporidiosis | Carcinoma In Situ | DOCK8 Immunodeficiency Syndrome | Infantile Nephropathic Cystinosis | Kawasaki Disease | Basan Syndrome | Astigmatism | Pelvic Inflammatory Disease | Primary Sclerosing Cholangitis | Autosomal Recessive Spastic Paraplegia Type 35 | VACTERL/VATER Association | Okihiro Syndrome | Sarcoidosis, Pulmonary | Anuria | Giant Cell Glioblastoma | Hemochromatosis Type 1 | Antisocial Personality Disorder | Focal Dermal Hypoplasia | Hypophosphatemic Rickets, Autosomal Recessive, 1 | Bardet-Biedl Syndrome | Meesmann Corneal Dystrophy | Retinitis Pigmentosa 3 | Lipodystrophy | Neuroendocrine Cancer | Multiple Myeloma | Systemic Mastocytosis | Feingold Syndrome | Reflex Epilepsy | Combined Malonic And Methylmalonic Acidemia | Donnai-Barrow Syndrome | Acrodysostosis | Prediabetes | Gastroenteritis, Eosinophilic | Imerslund-Grasbeck Syndrome | Glioblastoma | Primary Progressive Nonfluent Aphasia | 3-methylglutaconic Aciduria Type IV | Poretti-Boltshauser Syndrome | Monilethrix | Primary Ovarian Insufficiency | Sporadic Inclusion Body Myositis | Cone Dystrophy | Smoldering Myeloma | Gray Platelet Syndrome | Periventricular Leukomalacia | Reticular Dysgenesis | Myopia | Hepatic Veno-occlusive Disease | Celiac Disease | Conjunctivitis | D-2-Hydroxyglutaric Aciduria | Greig Cephalopolysyndactyly Syndrome | Synovitis | Recurrent Respiratory Papillomatosis | Melanoma, Malignant | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Nasodigitoacoustic Syndrome | Alopecia Totalis | Turner's Syndrome | Hereditary Folate Malabsorption | NDH Syndrome | Meningococcal Meningitis | Familial Dysautonomia | Aldosterone Deficiency | Obesity, Morbid | Erythrokeratodermia Variabilis | Dengue Hemorrhagic Fever | Vasculitis | Metanephric Adenoma | Xeroderma Pigmentosum Variant Type | Marinesco-Sjogren Syndrome | Anti-glomerular Basement Membrane Disease | Trichomegaly | Nutrition Disorders | Cutaneous Angiosarcoma | Congenital Myopathy | Intracerebral Hemorrhage | Graves Disease | Cryoglobulinemia | Tyrosine Hydroxylase Deficiency | Epithelial-myoepithelial Carcinoma | Sleep Disorder | Prolactinoma | Macular Corneal Dystrophy | Polymyositis | Optic Nerve Diseases | Cutaneous T-cell Lymphoma | Hereditary Neuropathy With Liability To Pressure Palsies | Lymphoma Lymphoblastic | Twin-to-twin Transfusion Syndrome | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Oculocutaneous Albinism | Acute Chest Syndrome | Porphyria | Hyperphosphatasia With Intellectual Disability Syndrome 4 | Ventricular Septal Defect | Hypereosinophilic Syndrome | Premature Ejaculation | Joubert Syndrome | Transient Bullous Dermolysis Of The Newborn | Silver-Russell Syndrome | Chondrodysplasia Punctata 1, X-linked Recessive | Congenital Disorders Of Glycosylation Type II | Sarcoma, Endometrial Stromal | Basal Cell Nevus Syndrome | Ichthyosis Bullosa Of Siemens | Hemorrhoids | Encephalopathy, Ethylmalonic | Osteogenesis Imperfecta | Paroxysmal Kinesigenic Dyskinesia | Leukemia | Encephalopathy, Hepatic | Pemphigoid | Nephrotic Syndrome | Superficial Spreading Melanoma | Conjunctivitis, Allergic | Osmotic Demyelination Syndrome | Alazami Syndrome | Carney Triad | IgA Deficiency | Blastomycosis | Mood Disorder | Eclampsia | Amblyopia | Lymphoma | Chorioretinitis | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Fanconi Anemia | Crohn's Disease | Schizoaffective Disorder | Kaposi Sarcoma | Duodenal Atresia | Mosaic Variegated Aneuploidy Syndrome 2 | Nicotine Addiction | Toxic Epidermal Necrolysis | Chronic Inflammatory Demyelinating Polyneuropathy | Gout | Hypokalemia | Otosclerosis | Anxiety Disorders | Rash | Danon Disease | Facioscapulohumeral Muscular Dystrophy Type 2 | Heart Block | Epidermolysis Bullosa Simplex, Dowling-Meara Type | Keratoconus | Conduct Disorder | Angioedema, Acquired | Adenoma, Pituitary | Esophageal Motility Disorders | Pericarditis | Episodic Ataxia | Sandhoff Disease | Mucolipidosis Type IV | Creatine Deficiency Syndrome | Micro Syndrome | Congenital Myasthenic Syndrome | Opisthorchiasis | Thanatophoric Dysplasia | Alpha-1 Antitrypsin Deficiency | Syphilis | Bare Lymphocyte Syndrome | Meconium Ileus | Cramp Fasciculation Syndrome | Agoraphobia | Dystrophy, Cone-rod | Zimmermann-Laband Syndrome | DNA Ligase IV Deficiency | Alpers Syndrome | Osteitis | Gardner Syndrome | Histiocytic Sarcoma | Lipoma | Tonsillitis | Charcot-Marie-Tooth Disease Type 2E | Tay-Sachs Disease | Bronchitis | Lattice Corneal Dystrophy | Primary Hyperoxaluria Type 3 | Japanese Encephalitis | Spinocerebellar Ataxia | Prurigo Nodularis | Melanocytic Nevus | Carcinoma, Transitional Cell | Malignant Peripheral Nerve Sheath Tumor | Bartsocas-Papas Syndrome | Atopic Dermatitis | Bloom Syndrome | Chylothorax, Congenital | Spinocerebellar Ataxia Type 14 | Epidermolytic Ichthyosis, Annular | Seasonal Mood Disorder | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Angioedema | Castleman Disease | Kernicterus | Liddle Syndrome | Lymphoproliferative Disorders | Vitelliform Macular Dystrophy | Vitreoretinopathy, Proliferative | Hydrocephalus | Asthma | Neurogenic Bladder | Cerebrovascular Disorders | Vitamin K Deficiency | Blepharospasm | Gastrointestinal Disorders | Shock, Cardiogenic | Graft-versus-host Disease | Spinocerebellar Ataxia Type 40 | Bacterial Meningitis | Benign Familial Neonatal Convulsions | Spondylometaphyseal Dysplasia | Van Der Knaap Disease | Intestinal Pseudo-obstruction | Anorchia | Maternally Inherited Diabetes And Deafness | Osteoglophonic Dysplasia | Lateral Meningocele Syndrome | Neuroleptic Malignant Syndrome | Lymphoproliferative Disease, X-linked | Meningeal Melanocytoma | Malaria | Blue Nevus | Ichthyosis | Diastrophic Dysplasia | Polycythemia Vera | VACTERL Association | Branchiootorenal Syndrome | Argininosuccinic Aciduria | Pseudoachondroplasia | Wolman Disease | Lung Diseases | Retinitis Pigmentosa | Epilepsy, Generalized | Pure Red Cell Aplasia | Myasthenia Gravis | Coloboma | Thalassemia | Compartment Syndrome | Cranioectodermal Dysplasia | Esophageal Carcinoma | Epidermolysis Bullosa Simplex | Ocular Hypertension | Hairy Cell Leukemia | Intracranial Hypertension | Ophthalmia, Sympathetic | Omenn Syndrome | Cystinosis | Dysplastic Nevus | Leber Hereditary Optic Neuropathy | Pituitary Disorders | Retinal Degeneration | Enlarged Vestibular Aqueduct | Acute Tubular Necrosis | Angioedema, Hereditary | Pseudoexfoliation Syndrome | Spondyloarthritis | Hyper IgE Syndrome | Peutz-Jeghers Syndrome | Giant Axonal Neuropathy | Clouston Hidrotic Ectodermal Dysplasia | Urofacial Syndrome | Lathosterolosis | Familial Mediterranean Fever | Vascular Calcification | Pulmonary Alveolar Microlithiasis | Neutrophilia | Specific Granule Deficiency | Familial Hemiplegic Migraine | Coronary Heart Disease | Hepatitis, Chronic | Esophagitis, Eosinophilic | Vulvovaginitis | Congenital Hemolytic Anemia | Liver Failure, Acute Infantile | Thrombocytopenia | Atrial Septal Defect | Congenital Fiber-type Disproportion Myopathy | Glycogen Storage Disease Type 3 | Cabezas Syndrome | Familial Male-limited Precocious Puberty | Cutaneous Lupus Erythematosus | Spastic Paraplegia Type 7 | Hennekam Lymphangiectasia-lymphedema Syndrome | Pineoblastoma | Tyrosinemia Type 1 | Anosmia, Congenital | Cold Agglutinin Disease | Porphyria, Variegate