Parvovirus B19 Infection

About the Disease
Erythema Infectiosum, also known as fifth disease, is related to pure red-cell aplasia and anemia, autoimmune hemolytic, and has symptoms including exanthema, fever and pruritus. An important gene associated with Erythema Infectiosum is CD40LG (CD40 Ligand), and among its related pathways/superpathways are Hematopoietic Stem Cells and Lineage-specific Markers and A-beta Uptake and Degradation. The drugs MF59 oil emulsion and Vaccines have been mentioned in the context of this disorder. Affiliated tissues include skin, bone marrow and bone.

Common Targets
PTPRS

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Achromatopsia | Alveolar Capillary Dysplasia | Combined Deficiency Of Factor V And Factor VIII | Eccrine Porocarcinoma | Ulcerative Colitis | Hemolytic Uremic Syndrome, Atypical | Carbamoyl Phosphate Synthetase I Deficiency | Hepatic Steatosis | Orotic Aciduria | Crouzon Syndrome With Acanthosis Nigricans | Whipple's Disease | Diabetic Neuropathy | Primary Hyperoxaluria Type 1 | Giant Cell Glioblastoma | Hepatic Veno-occlusive Disease | Cancer, Kidney | Glaucomatocyclitic Crisis | Impulse Control Disorder | Ileitis | IgA Deficiency | Keratitis-ichthyosis-deafness Syndrome | Reticular Dysgenesis | Nevus | Precocious Puberty | Charcot-Marie-Tooth Disease Type 4B1 | Niemann-Pick Disease, Type A | Neonatal Progeroid Syndrome | Nephropathy | Porphyria | Membranous Nephropathy | Presbyopia | Early Infantile Epileptic Encephalopathy | Myopia | Neuroma | Greig Cephalopolysyndactyly Syndrome | Senior-Loken Syndrome | Rickets | Liddle Syndrome | Meniere's Disease | Hepatitis | Castleman Disease | Skin Fragility-woolly Hair Syndrome | Congenital Sodium Diarrhea | Neurogenic Bladder | Fascioliasis | Macular Degeneration | Essential Fructosuria | Cerebellar Ataxia, Cayman Type | Early Infantile Epileptic Encephalopathy 4 | Chloridorrhea, Congenital | Xeroderma Pigmentosum Variant Type | Neural Tube Defect | AIDS | Acute Generalized Exanthematous Pustulosis | Obsessive-compulsive Disorder | Cancer, Skin | Takotsubo Cardiomyopathy | Osteogenesis Imperfecta Type II | Congenital Heart Block | Hyperglycemia | 3C Syndrome | Intermittent Explosive Disorder | Leukemia-lymphoma, Adult T-cell | Panic Disorder | Stargardt Disease | Oligodendroglioma | Congenital Aniridia | Lennox-Gastaut Syndrome | 3-hydroxy-3-methylglutaric Aciduria | Spinal Muscular Atrophy | Spinocerebellar Ataxia Type 21 | Hereditary Neuropathy With Liability To Pressure Palsies | Granuloma Annulare | Cerebrotendinous Xanthomatosis | Lipid Metabolism Disorders | Erdheim-Chester Disease | Charcot-Marie-Tooth Disease 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Prediabetes | Trichuriasis | Spinocerebellar Ataxia Type 12 | Thyroid Dysgenesis | Renal Hypouricemia | Juvenile Hyaline Fibromatosis | Teratozoospermia | DICER1 Syndrome | CDKL5 Deficiency Disorder | GATA2 Deficiency | Vitelliform Macular Dystrophy | High Molecular Weight Kininogen Deficiency | Congenital Dysfibrinogenemia | Spinocerebellar Ataxia Type 38 | Aarskog-Scott Syndrome | Burn-McKeown Syndrome | Heavy Chain Disease | Blue Rubber Bleb Nevus Syndrome | Ophthalmia, Sympathetic | H Syndrome | Polyarteritis Nodosa | Hypotrichosis | Rhizomelic Chondrodysplasia Punctata | Plasma Cell Dyscrasia | Inflammatory Joint Disease | Hypertensive Retinopathy | Hyperthyroidism | Tyrosine Hydroxylase Deficiency | Glaucoma, Congenital | Pituitary Dwarfism | Adenocarcinoma | Christianson Syndrome | Charcot-Marie-Tooth Disease, Type 1A | FG Syndrome | Peeling Skin Syndrome, Acral Type | Spondylolisthesis | Carcinoma, Signet Ring Cell | Mastitis | Hypertension, Portal | Sarcoidosis, Pulmonary | 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