Disease

Dowling-Degos Disease

About the Disease
Dowling-Degos Disease, also known as reticular pigment anomaly of flexures, is related to hidradenitis suppurativa and reticulate acropigmentation of kitamura. An important gene associated with Dowling-Degos Disease is POGLUT1 (Protein O-Glucosyltransferase 1), and among its related pathways/superpathways are Neuroscience and Pre-NOTCH Expression and Processing. Affiliated tissues include skin and liver, and related phenotypes are progressive reticulate hyperpigmentation and abnormality of the neck

Common Targets
POFUT1 | PSENEN

疾病靶点研报
Dowling-Degos Disease

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

Other Diseases

Hypophosphatemic Rickets, Autosomal Recessive, 1 | Hypokalemic Periodic Paralysis | Short-chain Acyl-CoA Dehydrogenase Deficiency | Distal Spinal Muscular Atrophy | Interstitial Lung Diseases | Incontinentia Pigmenti | Tay-Sachs Disease | VEXAS Syndrome | Wolfram Syndrome | Thyroiditis, Autoimmune | Dubin-Johnson Syndrome | Portal Vein Thrombosis | Colon Adenoma | Orotic Aciduria | Schwannomatosis | Non-proliferative Diabetic Retinopathy | Acute Lung Injury | Spinocerebellar Ataxia Type 38 | Carcinoma, Small Cell | Schizophrenia, Paranoid | Intestinal Pseudo-obstruction | CDKL5 Deficiency Disorder | Sickle Cell Disease | Fascioliasis | Aneurysm, Abdominal Aortic | Stuttering | Galactosemia | Nevus | Vitamin B12 Deficiency | Osteogenesis Imperfecta | Hypodontia | Mevalonate Kinase Deficiency | Eosinophilic Asthma | Ganglioglioma | Fabry's Disease | Pompe Disease | Hypomyelination With Atrophy Of Basal Ganglia And Cerebellum | Hartnup Disease | Osteitis | Choroiditis | Primary Lateral Sclerosis | Congenital Fiber-type Disproportion Myopathy | Van Der Knaap Disease | Moyamoya Disease | Blau Syndrome | Harlequin Ichthyosis | Best Macular Dystrophy | Prader-Willi Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Pathological Gambling | Haim-Munk Syndrome | Long QT Syndrome Type 2 | Congenital Torticollis | Methemoglobinemia | Stroke, Ischemic | Anti-NMDA Receptor Encephalitis | Sensorineural Hearing Loss | Priapism | Keratosis, Seborrheic | Crouzon Syndrome With Acanthosis Nigricans | Hyperparathyroidism, Primary | Cavitary Optic Disc Anomalies | Spinocerebellar Ataxia Type 21 | Guttate Psoriasis | Retinal Diseases | Diabetic Nephropathy | Megacystis-microcolon-intestinal Hypoperistalsis Syndrome | Dystonia | Small Lymphocytic Lymphoma | Bruck Syndrome | Cystitis | Chondroma | Tinea | Ependymoma | Wolman Disease | Rhabdoid Tumor | Hypervalinemia | Esophagitis, Eosinophilic | Hepatitis, Autoimmune | Barrett Esophagus | Myofibrillar Myopathy | Hyperparathyroidism, Secondary | Kernicterus | Hyperlipidemia Type V | Tonsillitis | Ichthyosis | Ectodermal Dysplasia | Hyperthyroidism | Leigh Syndrome | DICER1 Syndrome | Alveolar Capillary Dysplasia | T-cell Leukemia | Metanephric Adenoma | Fuchs Heterochromic Iridocyclitis | Salla Disease | Adenosine Deaminase Deficiency | Narcolepsy | GLUT1 Deficiency Syndrome | T-cell Lymphoma, Subcutaneous Panniculitis-like | Melnick-Needles Syndrome | Trichuriasis | Palsy, Cerebral | Ichthyosis Hystrix, Curth-Macklin Type | Mitochondrial Cytopathy | Esophageal Carcinoma | Micropenis | Transcobalamin Deficiency | Diastrophic Dysplasia | Hydrolethalus Syndrome | Exocrine Pancreatic Insufficiency | Saul-Wilson Syndrome | Spondyloperipheral Dysplasia | Delirium | Seizures | Charcot-Marie-Tooth Disease, Type 2C | Common Variable Immunodeficiency | Acute Motor Axonal Neuropathy | Cardiac Sarcoidosis | Osteoporosis-pseudoglioma Syndrome | Adenomyosis | Arthritis | Choroideremia | Primary Hyperoxaluria Type 1 | Dysequilibrium Syndrome | Speech Disorders | Multisystemic Smooth Muscle Dysfunction Syndrome | Hashimoto Thyroiditis | Liddle Syndrome | ACTH-independent Macronodular Adrenal Hyperplasia | Language Disorders | Congenital Bilateral Absence Of Vas Deferens | Angioedema | Androgen Insensitivity | Lattice Corneal Dystrophy Type 1 | Basal Ganglia Disease, Biotin-responsive | Alopecia Areata | Myelofibrosis | Scleritis | Otosclerosis | Spondylo-megaepiphyseal-metaphyseal Dysplasia | Vestibular Disease | Mycosis Fungoides | Prolidase Deficiency | Babesiosis | Infantile Liver Failure Syndrome 1 | Dupuytren Disease | Osteogenesis Imperfecta Type III | Cockayne Syndrome | Lymphangioleiomyomatosis | Pachyonychia Congenita | Tic Disorder | Unverricht-Lundborg Syndrome | Corticobasal Syndrome | Marinesco-Sjogren Syndrome | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Bullous Pemphigoid | Brugada Syndrome 1 | Sponastrime Dysplasia | Alopecia Totalis | Alexander Disease | Hypersensitivity | Encephalopathy | Papilledema | Obesity, Morbid | Plasma Cell Dyscrasia | Retinal Vasculitis | Alzheimer Disease, Late Onset | Aneurysm, Thoracic Aortic | Subcortical Band Heterotopia | Asplenia | Situs Inversus | Autoimmune Disease | Lymphangioma | Spondylocarpotarsal Synostosis Syndrome | Pulmonary Alveolar Microlithiasis | Oligodendroglioma | Impulse Control Disorder | Hypoparathyroidism | Fetal Alcohol Syndrome | Leukoencephalopathy, Progressive Multifocal | 17-beta-hydroxysteroid Dehydrogenase X Deficiency | WAGR Syndrome | Iron Overload | Learning Disability | Arthritis, Psoriatic | Hepatitis | Hemorrhoids | Lymphoma, Mantle Cell | Intracranial Hypertension | Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive 1 | Angioedema, Hereditary | Microphthalmia, Syndromic 7 | Chylothorax, Congenital | Congenital Stationary Night Blindness | Hereditary Pyropoikilocytosis | Histiocytic Sarcoma | Neuroendocrine Cancer | Gestational Trophoblastic Disease | Mucolipidosis Type II | Cranial Nerve Disease | Retinitis Pigmentosa 3 | Bartsocas-Papas Syndrome | Myoclonic Epilepsy With Ragged Red Fibers | Keratitis-ichthyosis-deafness Syndrome | Raynaud Phenomenon | Bietti Crystalline Dystrophy | Congestive Heart Failure | Blue Nevus | Pituitary Stalk Interruption Syndrome | Pitt-Hopkins Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Senior-Loken Syndrome | Psoriasis | Proteus Syndrome | Meningioma | Enterocolitis, Necrotizing | Glycogen Storage Disease Type 0, Muscle | Charcot-Marie-Tooth Disease Type 2T | Double Outlet Right Ventricle | Amyotrophic Lateral Sclerosis, Juvenile | Aspergillosis | Marshall-Smith Syndrome | Peripheral Neuropathy | Spinocerebellar Ataxia Type 31 | Giant Axonal Neuropathy | Neuroma | Dysfibrinogenemia | Cutaneous Angiosarcoma | Hypophosphatemic Rickets With Hypercalciuria, Hereditary | Ophthalmia, Sympathetic | Charcot-Marie-Tooth Disease, Type 1A | Campomelic Dysplasia | Crisponi Syndrome | Inflammatory Joint Disease | Creutzfeldt-Jakob Disease | Hepatic Veno-occlusive Disease | Hemangioma | Progressive Encephalopathy-optic Atrophy Syndrome | CREST Syndrome | Lesch-Nyhan Syndrome | Oculocutaneous Albinism | Pernicious Anemia | Noonan Syndrome-like Disorder With Loose Anagen Hair | Jacobsen Syndrome | Poretti-Boltshauser Syndrome | Intermittent Explosive Disorder | Colitis | Uremic Pruritus | Intellectual Disability, Autosomal Dominant 5 | Cerebrovascular Disorders | Primary Hyperoxaluria Type 3 | Poirier-Bienvenu Neurodevelopmental Syndrome | Hypertrophy | Cryptorchidism | Pelvic Inflammatory Disease | Carpenter Syndrome | Chronic Periodontitis | Perivascular Epithelioid Cell Tumor | Tangier Disease | Tenosynovial Giant Cell Tumor | Ameloblastic Carcinoma | Epidermolysis Bullosa Simplex, Generalized | Systemic Lupus Erythematosus | Intermittent Claudication | Generalized Epilepsy With Febrile Seizures Plus | Achondrogenesis | Hemoglobinopathies | Acromesomelic Dysplasia | Filariasis | Niemann-Pick Disease, Type A | Tricho-hepato-enteric Syndrome | Jaundice, Obstructive | Pulmonary Capillary Hemangiomatosis | Orthostatic Intolerance | Pigment Dispersion Syndrome | Sialidosis | Takenouchi-Kosaki Syndrome | Non-Hodgkin Lymphoma | Melanocytic Nevus | X-linked Acrogigantism | Spinocerebellar Ataxia Type 10 | Greig Cephalopolysyndactyly Syndrome | Spinal Cord Diseases | Multiple System Atrophy | Spondylosis | Knobloch Syndrome | Progressive Familial Intrahepatic Cholestasis Type 3 | Wolff-Parkinson-White Syndrome | Nijmegen Breakage Syndrome | Sezary Syndrome | Retinopathy Of Prematurity | Pericarditis | Sleep Apnea | Osteopathia Striata With Cranial Sclerosis | Antisocial Personality Disorder | Tylosis With Esophageal Cancer | Colitis, Collagenous | Hyperuricemic Nephropathy, Familial Juvenile | Rash | Epidermolysis Bullosa Simplex | Antisynthetase Syndrome | Melanoma, Malignant | Plasma Cell Leukemia | Niemann-Pick Disease, Type C | Autism | Chitayat Syndrome | Seborrheic Dermatitis | Viral Meningitis | Spinal And Bulbar Muscular Atrophy | Lactose Intolerance | Chloridorrhea, Congenital | 3-methylcrotonyl-CoA Carboxylase Deficiency | Cold-induced Sweating Syndrome | Reflex Epilepsy | VACTERL Association | Frontometaphyseal Dysplasia | Focal Dermal Hypoplasia | Japanese Encephalitis | Hyperkeratosis | Esthesioneuroblastoma | Lipid Storage Myopathy | Cluster Headache | Trismus-pseudocamptodactyly Syndrome | Bloom Syndrome | Genee-Wiedemann Syndrome | Familial Dysautonomia | Sialidosis Type I | Dyggve-Melchior-Clausen Disease | Atrioventricular Septal Defect | Tendinopathy | Cerebrotendinous Xanthomatosis | Coffin-Lowry Syndrome | Endophthalmitis | Alpha-mannosidosis | Vitelliform Macular Dystrophy | Disseminated Intravascular Coagulation | Hemorrhage | Amblyopia | Polyarteritis Nodosa | Wieacker-Wolff Syndrome | Chronic Neutrophilic Leukemia | Congenital Muscular Dystrophy | Congenital Dysfibrinogenemia | Woodhouse-Sakati Syndrome | Thalassemia | Purpura | Porphyria | Arthritis, Reactive | Avellino Corneal Dystrophy | Hypertelorism | Hydrocephalus, Normal Pressure | Cholangiocarcinoma | Whipple's Disease | Primary Progressive Aphasia | Glutaric Aciduria Type 2 | Aldosteronism | Premenstrual Syndrome | Hypotrichosis, Congenital, With Juvenile Macular Dystrophy | Mitochondrial DNA Depletion Syndrome 13 | Kaposiform Hemangioendothelioma | Aphasia | Waardenburg Syndrome Type 4 | Keratoconus | Microtia | Mandibuloacral Dysplasia With Type A Lipodystrophy | Neurogenic Bladder | DNA Ligase IV Deficiency | Inflammatory Linear Verrucous Epidermal Nevus | Porencephaly | Polyomavirus Nephropathy | Hartsfield Syndrome | Occipital Neuralgia | Progressive Familial Intrahepatic Cholestasis | Lipid Metabolism Disorders | Purpura, Thrombotic Thrombocytopenic | Mast Cell Leukemia | Temtamy Preaxial Brachydactyly Syndrome | Dystonia-parkinsonism, X-linked | Dental Caries | Hypogammaglobulinemia | Aplasia Cutis Congenita | Esophageal Motility Disorders | Periventricular Nodular Heterotopia | Congenital Nystagmus | Metachromatic Leukodystrophy | Nephritis, Interstitial | Cholestasis, Intrahepatic | Crimean-Congo Hemorrhagic Fever | Hypertension, Essential | Cardiofaciocutaneous Syndrome | Aldosterone Synthase Deficiency | Spondylometaphyseal Dysplasia | Primary Aldosteronism | Myoclonus | Celiac Disease | Pulmonary Stenosis | Fahr Disease | Early Infantile Epileptic Encephalopathy 28 | Low Phospholipid Associated Cholelithiasis | Major Depression