Glycogen Storage Disease Type VIII [glykogenóza typu VIII]

topical
Terms

glykogen - nemoc z ukládání typ VIII

 

Glycogenosis 8

Persistent link   https://www.medvik.cz/link/D006015
Definition

An 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.

Annotation
do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D006015 MeSH Browser
CUI
M0009476
Previous indexing
Glycogenosis (1966-1974)
History note
91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 8 see under GLYCOGENOSIS 1975-88
Online note
use GLYCOGEN STORAGE DISEASE TYPE VIII to search GLYCOGENOSIS 8 1975-88
Public note
91; was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 8 see under GLYCOGENOSIS 1975-88

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.322 Genetic Diseases, X-Linked 59
C16.320.322.030 Aicardi Syndrome
C16.320.322.061 Androgen-Insensitivity Syndrome 56
C16.320.322.068 Barth Syndrome 6
C16.320.322.076 Bulbo-Spinal Atrophy, X-Linked 8
C16.320.322.092 Choroideremia 3
C16.320.322.100 Dent Disease 1
C16.320.322.108 Dyskeratosis Congenita 9
C16.320.322.116 Ectodermal Dysplasia 1, Anhidrotic 3
C16.320.322.124 Fabry Disease 187
C16.320.322.186 Focal Dermal Hypoplasia 6
C16.320.322.201 Glycogen Storage Disease Type IIb 11
C16.320.322.217 Glycogen Storage Disease Type VIII
C16.320.322.233 Granulomatous Disease, Chronic 54
C16.320.322.235 Hemophilia B 214
C16.320.322.237 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
C16.320.322.241 Ichthyosis, X-Linked 9
C16.320.322.370 Isolated Noncompaction of the Ventricular Myocardium 11
C16.320.322.500 X-Linked Intellectual Disability 17
C16.320.322.562 Muscular Dystrophy, Duchenne 133
C16.320.322.625 Muscular Dystrophy, Emery-Dreifuss 18
C16.320.322.750 Oculocerebrorenal Syndrome 9
C16.320.322.828 Ornithine Carbamoyltransferase Deficiency Disease 19
C16.320.322.906 Pelizaeus-Merzbacher Disease 11
C16.320.322.937 Wiskott-Aldrich Syndrome 20
C16.320.322.968 X-Linked Combined Immunodeficiency Diseases 4
C16.320.565 Metabolism, Inborn Errors 711
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors 36
C16.320.565.202.449 Glycogen Storage Disease 44
C16.320.565.202.449.448 Glycogen Storage Disease Type I 15
C16.320.565.202.449.500 Glycogen Storage Disease Type II 59
C16.320.565.202.449.510 Glycogen Storage Disease Type IIb 11
C16.320.565.202.449.520 Glycogen Storage Disease Type III 8
C16.320.565.202.449.540 Glycogen Storage Disease Type IV 1
C16.320.565.202.449.560 Glycogen Storage Disease Type V
C16.320.565.202.449.580 Glycogen Storage Disease Type VI
C16.320.565.202.449.600 Glycogen Storage Disease Type VII
C16.320.565.202.449.620 Glycogen Storage Disease Type VIII
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 196
C18.452.648 Metabolism, Inborn Errors 711
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors 36
C18.452.648.202.449 Glycogen Storage Disease 44
C18.452.648.202.449.448 Glycogen Storage Disease Type I 15
C18.452.648.202.449.500 Glycogen Storage Disease Type II 59
C18.452.648.202.449.510 Glycogen Storage Disease Type IIb 11
C18.452.648.202.449.520 Glycogen Storage Disease Type III 8
C18.452.648.202.449.540 Glycogen Storage Disease Type IV 1
C18.452.648.202.449.560 Glycogen Storage Disease Type V
C18.452.648.202.449.580 Glycogen Storage Disease Type VI
C18.452.648.202.449.600 Glycogen Storage Disease Type VII
C18.452.648.202.449.620 Glycogen Storage Disease Type VIII

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