Glycogen Storage Disease [glykogenóza]

topical
45
Terms

glykogen - nemoc z ukládání
porucha ukládání glykogenu
poruchy ukládání glykogenu

 

Glycogenosis

Persistent link   https://www.medvik.cz/link/D006008
Definition

A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.

Annotation
an inborn error of carbohydrate metab; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D006008 MeSH Browser
CUI
M0009469
History note
89; was GLYCOGENOSIS 1963-88
Online note
use GLYCOGEN STORAGE DISEASE to search GLYCOGENOSIS 1966-88
Public note
89; was GLYCOGENOSIS 1963-88

C Diseases
C16.320.565.202.303 Fucosidosis 2
C16.320.565.202.355 Galactosemias 44
C16.320.565.202.449 Glycogen Storage Disease 45
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
C16.320.565.202.460 Hyperoxaluria, Primary 10
C16.320.565.202.589 Lactose Intolerance 132
C16.320.565.202.607 Mannosidase Deficiency Diseases 1
C16.320.565.202.670 Mucolipidoses 10
C16.320.565.202.715 Mucopolysaccharidoses 81
C18.452 Metabolic Diseases 1 200
C18.452.648.202.303 Fucosidosis 2
C18.452.648.202.355 Galactosemias 44
C18.452.648.202.449 Glycogen Storage Disease 45
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
C18.452.648.202.460 Hyperoxaluria, Primary 10
C18.452.648.202.589 Lactose Intolerance 132
C18.452.648.202.607 Mannosidase Deficiency Diseases 1
C18.452.648.202.670 Mucolipidoses 10
C18.452.648.202.715 Mucopolysaccharidoses 81

Glycogen Storage Disease 0, Liver Disease MeSH Browser

Glycogen Storage Disease 0, Muscle Disease MeSH Browser

Glycogen Storage Disease IC Disease MeSH Browser

Glycogen Storage Disease IXB Disease MeSH Browser

Glycogen Storage Disease IXC Disease MeSH Browser

Glycogen Storage Disease Type Ix Disease MeSH Browser

Glycogen Storage Disease XII Disease MeSH Browser

Glycogen Storage Disease XIII Disease MeSH Browser

Glycogen Storage Disease XIV Disease MeSH Browser

Glycogen Storage Disease of Heart, Lethal Congenital Disease MeSH Browser

Glycogen Storage Disease, Type IXA2 Disease MeSH Browser

Glycogen Storage Disease, Type IXD Disease MeSH Browser

Lactate dehydrogenase deficiency type A Disease MeSH Browser

Liver Glycogenosis, X-Linked, Type II Disease MeSH Browser

Polyglucosan Body Disease, Adult Form Disease MeSH Browser