Herpes Genitalis

About the Disease
Genital Herpes, also known as herpes genitalis, is related to herpes simplex and chancroid, and has symptoms including sores, fever and swollen glands. An important gene associated with Genital Herpes is ACKR1 (Atypical Chemokine Receptor 1 (Duffy Blood Group)), and among its related pathways/superpathways are Innate Immune System and MIF Mediated Glucocorticoid Regulation. The drugs Famciclovir and Acyclovir have been mentioned in the context of this disorder. Affiliated tissues include genital system, rectum and t cells, and related phenotypes are homeostasis/metabolism and immune system

Common Targets
PGR | IFI16 | IFNG | Interferon (nonspecified subtype) | G7099 | TLR7 | TLR8 | DNA-Directed DNA Polymerase Complex | G3569

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Other Diseases

Jalili Syndrome | Postpartum Depression | Angioimmunoblastic T-cell Lymphoma | WAGR Syndrome | Polycythemia | Pitt-Hopkins Syndrome | Polycystic Liver | Seminoma | Chitayat Syndrome | Pulmonary Tuberculosis | Arteriovenous Malformations | Bainbridge-Ropers Syndrome | Paraganglioma | Lyme Disease | Smoldering Myeloma | GLUT1 Deficiency Syndrome | Adrenoleukodystrophy, X-linked | Pyruvate Kinase Deficiency | Metanephric Adenoma | Erectile Dysfunction | Orthostatic Intolerance | Urofacial Syndrome | Reticular Dysgenesis | Mannosidase Deficiency Diseases | Cyst | Allan-Herndon-Dudley Syndrome | Retinal Dystrophy, Early-onset Severe | Hairy Cell Leukemia | Atelosteogenesis Type 1 | Choroiditis | Myotonic Disorders | Premature Ejaculation | Myelitis, Transverse | Vitamin B12 Deficiency | Metabolic Diseases | Lamellar Ichthyosis | Vaginitis | Scabies | Juvenile Xanthogranuloma | Supravalvular Aortic Stenosis | Bursitis | Hereditary Elliptocytosis | Cancer, Brain | Tracheal Disorders | Lymphoproliferative Disorders | Acute Generalized Exanthematous Pustulosis | Acute Tubular Necrosis | Poirier-Bienvenu Neurodevelopmental Syndrome | Congenital Hypofibrinogenemia | Scleritis | Creatine Deficiency Syndrome Due To AGAT Deficiency | Larsen Syndrome | Phenylketonuria | 3-methylcrotonyl-CoA Carboxylase Deficiency | Primary Torsion Dystonia | Esophageal Adenocarcinoma | Corneal Dystrophies, Hereditary | Periodic Limb Movement Disorder | Marinesco-Sjogren Syndrome | Macrophagic Myofasciitis | Alexander Disease | Sponastrime Dysplasia | Hypokalemia | Waardenburg Syndrome Type 2 | Cone Dystrophy | Apparent Mineralocorticoid Excess Syndrome | Pelizaeus-Merzbacher Disease | Alpha-1 Antitrypsin Deficiency | Malaria | Chondrodysplasia Punctata 1, X-linked Recessive | Porokeratosis | Neutropenia | Kleine-Levin Syndrome | Lipid Metabolism Disorders | Xeroderma Pigmentosum | Eosinophilic Asthma | Mevalonate Kinase Deficiency | Chromosome 17q21.31 Deletion Syndrome | Trichotillomania | Periventricular Nodular Heterotopia | Congenital Ichthyosiform Erythroderma | Idiopathic Pulmonary Fibrosis | AIDS | Lymphangioleiomyomatosis | Chronic Mucocutaneous Candidiasis | Down Syndrome | Hypogonadism | Pemphigus | Vestibular Disease | Rift Valley Fever | Paracoccidioidomycosis | Retinal Degeneration | Progressive Familial Intrahepatic Cholestasis Type 3 | Hereditary Spherocytosis | Inflammatory Myopathy | McKusick Type Metaphyseal Chondrodysplasia | Splenomegaly | Spondylocostal Dysostosis | Spinal Muscular Atrophy Type 3 | Gastrointestinal Disorders | Hennekam Lymphangiectasia-lymphedema Syndrome | Keloid | Medulloblastoma | Charcot-Marie-Tooth Disease Type 2D | Hypospadias | Retinal Telangiectasia | Familial Hemiplegic Migraine | Hepatitis, Autoimmune | Hepatitis B, Chronic | Apert Syndrome | Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form | Overactive Bladder | Sezary Syndrome | Chanarin-Dorfman Syndrome | Intellectual Disability, Autosomal Dominant 5 | 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Leishmaniasis, Cutaneous | MELAS Syndrome | GM2-gangliosidosis AB Variant | Light Chain Amyloidosis | Silicosis | Multiple System Atrophy | Meier-Gorlin Syndrome | Posterior Polar Cataract | Chronic Thromboembolic Pulmonary Hypertension | Diabetes Insipidus, Neurogenic | Warsaw Breakage Syndrome | Hyperkalemic Periodic Paralysis | Synovitis | Thyrotoxic Periodic Paralysis | Spinocerebellar Ataxia | Pathological Gambling | CHOPS Syndrome | Ectopia Lentis, Isolated, Autosomal Recessive | Fabry's Disease | Sorsby Fundus Dystrophy | Hyperbilirubinemia, Neonatal | Pityriasis Rubra Pilaris | Cherubism | Carcinoma, Squamous Cell | Congenital Adrenal Hyperplasia | Multifocal Motor Neuropathy | Chronic Leukemia | 3-hydroxy-3-methylglutaric Aciduria | Behcet's Disease | Antiphospholipid Syndrome | Kidney Stones | McCune-Albright Syndrome | Superficial Spreading Melanoma | Cartilage Disorders | Dysgerminoma | Hepatitis D | Paget's Disease Of The Breast | Thromboembolism | Vitiligo | Inflammatory 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