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Glycogen Storage Disease Type VIII
MeSH HeadingGlycogen Storage Disease Type VIII
Tree NumberC16.320.322.217
Tree NumberC16.320.565.202.449.620
Tree NumberC18.452.648.202.449.620
Annotationdo not use / congen & do not coord with INFANT, NEWBORN, DISEASES
Scope NoteAn x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively mild; hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present. Liver shrinkage occurs in response to glucagon.
Entry TermGlycogenosis 8
Allowable QualifiersBL CF CI CL CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Entry VersionGLYCOGEN STORAGE DIS VIII
Previous Indexing Glycogenosis (1966-1974)
Online Noteuse GLYCOGEN STORAGE DISEASE TYPE VIII to search GLYCOGENOSIS 8 1975-88
History Note91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 8 see under GLYCOGENOSIS 1975-88
Date of Entry19741212
Unique IDD006015


MeSH Tree Structures

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Genetic Diseases, X-Linked [C16.320.322]
Aicardi Syndrome [C16.320.322.030]
Androgen-Insensitivity Syndrome [C16.320.322.061]
Barth Syndrome [C16.320.322.068]
Bulbo-Spinal Atrophy, X-Linked [C16.320.322.076]
Choroideremia [C16.320.322.092]
Dent Disease [C16.320.322.100]
Dyskeratosis Congenita [C16.320.322.108]
Ectodermal Dysplasia 1, Anhidrotic [C16.320.322.116]
Fabry Disease [C16.320.322.124]
Focal Dermal Hypoplasia [C16.320.322.186]
Glycogen Storage Disease Type IIb [C16.320.322.201]
Arrow pointing to current tree nodeGlycogen Storage Disease Type VIII [C16.320.322.217]
Granulomatous Disease, Chronic [C16.320.322.233]
Hemophilia B [C16.320.322.235]
Hyper-IgM Immunodeficiency Syndrome, Type 1 [C16.320.322.237]
Hypophosphatemic Rickets, X-Linked Dominant [C16.320.322.239]
Ichthyosis, X-Linked [C16.320.322.241]
Isolated Noncompaction of the Ventricular Myocardium [C16.320.322.370]
Mental Retardation, X-Linked [C16.320.322.500]  +
Muscular Dystrophy, Duchenne [C16.320.322.562]
Muscular Dystrophy, Emery-Dreifuss [C16.320.322.625]
Oculocerebrorenal Syndrome [C16.320.322.750]
Ornithine Carbamoyltransferase Deficiency Disease [C16.320.322.828]
Pelizaeus-Merzbacher Disease [C16.320.322.906]
Wiskott-Aldrich Syndrome [C16.320.322.937]
X-Linked Combined Immunodeficiency Diseases [C16.320.322.968]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Metabolism, Inborn Errors [C16.320.565]
         Carbohydrate Metabolism, Inborn Errors [C16.320.565.202]
            Glycogen Storage Disease [C16.320.565.202.449]
Glycogen Storage Disease Type I [C16.320.565.202.449.448]
Glycogen Storage Disease Type II [C16.320.565.202.449.500]
Glycogen Storage Disease Type IIb [C16.320.565.202.449.510]
Glycogen Storage Disease Type III [C16.320.565.202.449.520]
Glycogen Storage Disease Type IV [C16.320.565.202.449.540]
Glycogen Storage Disease Type V [C16.320.565.202.449.560]
Glycogen Storage Disease Type VI [C16.320.565.202.449.580]
Glycogen Storage Disease Type VII [C16.320.565.202.449.600]
Arrow pointing to current tree nodeGlycogen Storage Disease Type VIII [C16.320.565.202.449.620]

 
Nutritional and Metabolic Diseases [C18]
   Metabolic Diseases [C18.452]
      Metabolism, Inborn Errors [C18.452.648]
         Carbohydrate Metabolism, Inborn Errors [C18.452.648.202]
            Glycogen Storage Disease [C18.452.648.202.449]
Glycogen Storage Disease Type I [C18.452.648.202.449.448]
Glycogen Storage Disease Type II [C18.452.648.202.449.500]
Glycogen Storage Disease Type IIb [C18.452.648.202.449.510]
Glycogen Storage Disease Type III [C18.452.648.202.449.520]
Glycogen Storage Disease Type IV [C18.452.648.202.449.540]
Glycogen Storage Disease Type V [C18.452.648.202.449.560]
Glycogen Storage Disease Type VI [C18.452.648.202.449.580]
Glycogen Storage Disease Type VII [C18.452.648.202.449.600]
Arrow pointing to current tree nodeGlycogen Storage Disease Type VIII [C18.452.648.202.449.620]

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