Disease

Hypotrichosis

About the Disease
Hypotrichosis is related to hypotrichosis 7 and hypotrichosis, congenital, with juvenile macular dystrophy. An important gene associated with Hypotrichosis is HYPT9 (Hypotrichosis 9), and among its related pathways/superpathways is Keratinization. The drugs Bimatoprost and Minoxidil have been mentioned in the context of this disorder. Affiliated tissues include skin, bone and bone marrow, and related phenotypes are endocrine/exocrine gland and integument

Common Targets
TKFC | PTGER1 | MMP14

疾病靶点研报
Hypotrichosis

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

Other Diseases

FG Syndrome | Leprosy | Cervicitis | Kindler Syndrome | Brenner Tumor | Angelman Syndrome | Bruck Syndrome | Otosclerosis | Waardenburg Syndrome Type 2 | Glycogen Storage Disease Type 1a | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Cornelia De Lange Syndrome | Craniometaphyseal Dysplasia | Weill-Marchesani Syndrome | Aplastic Anemia | Hemosiderosis | Autosomal Recessive Bestrophinopathy | Keratosis | Cancer, Colon | Mannosidase Deficiency Diseases | Neurofibromatosis | Rolandic Epilepsy | Hereditary Hemorrhagic Telangiectasia Type 2 | Extramammary Paget's Disease | Cri-du-chat Syndrome | Niemann-Pick Disease, Type B | Liebenberg Syndrome | Osteoporosis-pseudoglioma Syndrome | Canavan Disease | Hemangioblastoma | Shwachman-Bodian-Diamond Syndrome | Retinitis | Blepharo-cheilo-odontic Syndrome | Colitis, Collagenous | Poikiloderma With Neutropenia | Intestinal Tuberculosis | Stargardt Disease | Thanatophoric Dysplasia | Pseudoachondroplasia | Aplasia Cutis Congenita | Osmotic Demyelination Syndrome | Pontocerebellar Hypoplasia Type 7 | Leukemia | Spinocerebellar Ataxia Type 23 | Hyperbilirubinemia | Retinopathy Of Prematurity | Congenital Bilateral Absence Of Vas Deferens | Leukoplakia | Nephroblastoma | Trichomegaly | Pulmonary Vein Stenosis | Multiple Sulfatase Deficiency | Spinocerebellar Ataxia Type 5 | Congenital Dyserythropoietic Anemia | Patent Foramen Ovale | VACTERL/VATER Association | Diabetes Type 2 | Erectile Dysfunction | Cholangitis | Congenital Dyserythropoietic Anemia Type 4 | Heimler Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Senior-Loken Syndrome | Fetal And Neonatal Alloimmune Thrombocytopenia | Hyperacusis | Tularemia | Angioimmunoblastic T-cell Lymphoma | Osteopathia Striata With Cranial Sclerosis | Cole-Carpenter Syndrome | Purpura, Thrombotic Thrombocytopenic | Infertility, Male | Hypohidrotic Ectodermal Dysplasia, X-linked | Warsaw Breakage Syndrome | Congenital Poikiloderma | Cryoglobulinemia | Sclerosteosis 2 | Prune Belly Syndrome | Fontaine Progeroid Syndrome | Intermittent Claudication | Barakat Syndrome | Richter's Syndrome | Hartnup Disease | Hemophagocytic Lymphohistiocytosis | Aicardi-Goutieres Syndrome | Intermittent Explosive Disorder | Microcephalic Primordial Dwarfism | Erysipelas | Porphyria, Variegate | Carcinoid Tumor | Majeed Syndrome | Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Gardner Syndrome | Platelet Disorders | Hyperinsulinism-hyperammonemia Syndrome | Heart Block | Porphyria Cutanea Tarda | Congenital Disorders Of Glycosylation Type II | Familial Exudative Vitreoretinopathy | Venous Insufficiency | Communication Disorders | Pontocerebellar Hypoplasia Type 2 | Cholelithiasis | Lichen Sclerosus | Adrenoleukodystrophy, X-linked | Charcot-Marie-Tooth Disease Type 2D | Thalassemia | Adenosine Deaminase Deficiency | Pain | Headache | Fibromuscular Dysplasia | Holt-Oram Syndrome | Schaaf-Yang Syndrome | Chiari Malformation Type I | Progressive Osseous Heteroplasia | Liddle Syndrome | Renal Medullary Carcinoma | Sickle Cell Anemia | Bipolar Disorder | Heavy Chain Disease | Chondrosarcoma | Waldenstrom Macroglobulinemia | Schindler Disease | Neonatal Progeroid Syndrome | Celiac Disease | IgA Deficiency | Meconium Ileus | Temporal Lobe Epilepsy | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Desbuquois Syndrome | Neurocutaneous Syndromes | Hyperkeratosis | Chronic Idiopathic Myelofibrosis | Sialoadenitis | Hypocalcemia | Intestinal Pseudo-obstruction | Mesothelioma, Malignant | Microcephaly | Glycogen Storage Disease Type 0 | Hypercholesterolemia | Spinocerebellar Ataxia Type 40 | Retinoblastoma | Cranial Nerve Disease | Benign Familial Infantile Seizures | Anxiety Disorders | Chronic Thromboembolic Pulmonary Hypertension | Keratocystic Odontogenic Tumor | Colitis, Lymphocytic | Mast Cell Leukemia | Fascioliasis | Hyperlipidemia Type V | Cardiospondylocarpofacial Syndrome | Niemann-Pick Disease, Type A | Inflammatory Myofibroblastic Tumor | Metatropic Dysplasia | Neurofibroma, Plexiform | Gnathodiaphyseal Dysplasia | Cutaneous Mastocytosis | Saul-Wilson Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Chronic Beryllium Disease | Erdheim-Chester Disease | Mumps | Carbonic Anhydrase VA Deficiency | Optic Nerve Diseases | Impulse Control Disorder | Adenomatoid Tumor | Molybdenum Cofactor Deficiency | Progressive Familial Intrahepatic Cholestasis Type 1 | Odonto-onycho-dermal Dysplasia | Basal Ganglia Disease | Cutaneous Angiosarcoma | Neuroblastoma | Congenital Primary Aphakia | Dystonia Musculorum Deformans | Glioma | Postpoliomyelitis Syndrome | Alexander Disease | Autoimmune Autonomic Ganglionopathy | Speech Disorders | Orthostatic Intolerance | Plasma Cell Leukemia | Progressive Familial Intrahepatic Cholestasis Type 2 | Cardiomyopathy, Peripartum | Myoclonus | Zygomycosis | Enlarged Vestibular Aqueduct | Aldosteronism | Guillain-Barre Syndrome | Myoclonic Atonic Epilepsy | Erythema Nodosum | Klinefelter Syndrome | Sleep Apnea, Obstructive | Dyggve-Melchior-Clausen Disease | Arrhythmogenic Right Ventricular Cardiomyopathy | Ollier Disease | Mastitis | Autosomal Recessive Spastic Paraplegia Type 75 | Proteasome-associated Autoinflammatory Syndrome 2 | Phosphoglycerate Dehydrogenase Deficiency | Hypertensive Retinopathy | Bloom Syndrome | Guanidinoacetate Methyltransferase Deficiency | Roberts Syndrome | Optic Atrophy 2 | Aceruloplasminemia | Chediak-Higashi Syndrome | Hypermetropia | Axenfeld-Rieger Syndrome | Autoimmune Disease | Impetigo | Panniculitis | Nager Acrofacial Dysostosis | Erythrokeratodermia Variabilis | Menetrier Disease | Major Depression | Hepatitis D | Charcot-Marie-Tooth Disease Axonal Type 2N | Pseudo-pseudohypoparathyroidism | Chronic Enteropathy Associated With SLCO2A1 Gene | Marshall-Smith Syndrome | Hypersensitivity | DRESS Syndrome | Enhanced S-cone Syndrome | Neuroendocrine Cancer | Wolcott-Rallison Syndrome | Hemolytic Uremic Syndrome | Chronic Myeloid Leukemia | Spinocerebellar Ataxia Type 1 | Hyperostosis | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Sezary Syndrome | Primary Progressive Aphasia | Heroin Dependence | Very Long-chain Acyl-CoA Dehydrogenase Deficiency | Premature Ejaculation | Proopiomelanocortin Deficiency | Niemann-Pick Disease | Macular Degeneration | Lathosterolosis | Lymphangioleiomyomatosis | Mohr-Tranebjaerg Syndrome | GATA2 Deficiency | Krabbe Disease | Specific Granule Deficiency | Hydronephrosis | Arthritis | Goiter, Nodular | Nail Disorder, Nonsyndromic Congenital | Dentinogenesis Imperfecta | Lichen Planus | Influenza | CREST Syndrome | Medulloblastoma | Pseudohypoparathyroidism Type 1B | Pierpont Syndrome | Hypophosphatasia | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Jalili Syndrome | Pachyonychia Congenita | HELLP Syndrome | Carcinoid Syndrome | Huntington's Disease | Polycystic Ovary Syndrome | Herpes Simplex Dermatitis | Cancer, Lung | Ocular Albinism Type 1 | Nicotine Addiction | Carcinoma, Merkel Cell | Congenital Nystagmus | Urticaria | Preaxial Polydactyly | Colon Adenoma | Common Cold | Rheumatoid Arthritis | VACTERL Association | Acute Generalized Exanthematous Pustulosis | Cushing Syndrome | Uveitis | Chorioretinitis | Hepatorenal Syndrome | Rett Syndrome | Chitayat Syndrome | Heterotaxy | Nail-Patella Syndrome | Lennox-Gastaut Syndrome | 3-M Syndrome | Hereditary Xerocytosis | Papillorenal Syndrome | Peripheral Neuropathy | Peeling Skin Syndrome, Acral Type | NGLY1 Deficiency | CHOPS Syndrome | Astrocytoma | Idiopathic Multicentric Castleman Disease | Keratosis, Actinic | Phenylketonuria II | Endometrial Hyperplasia | Autoimmune Hemolytic Anemia | LRBA Deficiency | Leber Hereditary Optic Neuropathy | Frank-ter Haar Syndrome | Adenylosuccinate Lyase Deficiency | Rhabdomyosarcoma, Embryonal | Vertebrobasilar Insufficiency | Trismus-pseudocamptodactyly Syndrome | Urolithiasis | Urofacial Syndrome | Colorectal Adenoma | Angioedema, Acquired | Pulmonary Stenosis | Otitis Externa | Pure Autonomic Failure | Menkes Disease | Lesch-Nyhan Syndrome | Pycnodysostosis | Borderline Personality Disorder | Tuberculous Meningitis | Fundus Albipunctatus | Glycogen Storage Disease Type 5 | Schistosomiasis Mansoni | Achondrogenesis | Kohlschutter-Tonz Syndrome | Alopecia | Facioscapulohumeral Muscular Dystrophy Type 1 | Hemorrhoids | Tinea Versicolor | Arteriovenous Malformations | Eczema | Seizures-scoliosis-macrocephaly Syndrome | Lymphoproliferative Disorders | Focal Cortical Dysplasia Type 2 | Creutzfeldt-Jakob Disease | Focal Segmental Glomerulosclerosis | Sarcosinemia | Ileitis | Cardiac Arrest | Clouston Hidrotic Ectodermal Dysplasia | Reticular Dysgenesis | Charcot-Marie-Tooth Disease, Type 2A | DICER1 Syndrome | Acne | Spastic Paraplegia Type 7 | Pitt-Hopkins Syndrome | Sarcoma, Alveolar Soft Part | Brachial Plexus Neuropathy | Oculocutaneous Albinism Type 2 | Lymphangioma | Erythematotelangiectatic Rosacea | Cranioectodermal Dysplasia | Angiomyolipoma | Nephronophthisis | Small Lymphocytic Lymphoma | Diverticulitis | Gastroenteritis | Sulfite Oxidase Deficiency | Creatine Deficiency Syndrome Due To AGAT Deficiency | Amyotrophic Lateral Sclerosis, Juvenile | Vascular Cognitive Impairment | Fibrodysplasia Ossificans Progressiva | Congenital Ichthyosiform Erythroderma | Choriocarcinoma | Atrioventricular Septal Defect | Trachoma | Hyperbilirubinemia, Neonatal | 3-methylglutaconic Aciduria Type I | Partington Syndrome | Hypobetalipoproteinemias | Arterial Tortuosity Syndrome | Focal Facial Dermal Dysplasia | McLeod Syndrome | Coronary Artery Disease | Kallmann Syndrome | Binge Eating Disorder | Malaria, Cerebral | Dermatomyositis | Schuurs-Hoeijmakers Syndrome | Neurofibromatosis Type 2 | Hypertensive Nephropathy | Reye Syndrome | Neurocysticercosis | Corneal Neovascularization | Antenatal Bartter Syndrome Type 1 | Osteosarcoma | Martsolf Syndrome | Liver Failure, Acute Infantile | Precocious Puberty | Gout | Sarcoidosis | Non-Hodgkin Lymphoma | Porphyria | Wieacker-Wolff Syndrome | Orotic Aciduria | Sick Sinus Syndrome 1 | Vitamin A Deficiency | Myofibromatosis | Biotinidase Deficiency | Systemic Lupus Erythematosus | Ectrodactyly | Hyperphenylalaninemia