Glycogen Storage Disease Type VI [glykogenóza typu VI]

topical
Terms

glykogen - nemoc z ukládání typ VI
glykogenóza typ 6
glykogenóza typ VI
glykogenóza VI
Hersova nemoc

 

Glycogenosis 6
Glycogenosis Type VI
Glycogenosis VI
Hepatic Glycogen Phosphorylase Deficiency
Hers Disease
Hers' Disease
Liver Phosphorylase Deficiency Syndrome

Persistent link   https://www.medvik.cz/link/D006013
Definition

A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.

DUI
D006013 MeSH Browser
CUI
M0009474
Previous indexing
Glycogenosis (1966-1974); Liver Diseases (1966-1974); Glucosyltransferases/metabolism (1966-1974)
History note
91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 6 see under GLYCOGENOSIS 1975-88
Online note
use GLYCOGEN STORAGE DISEASE TYPE VI to search GLYCOGENOSIS 6 1975-88
Public note
91; was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 6 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 1 215
C16.320.565 Metabolism, Inborn Errors 714
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors 36
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
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 200
C18.452.648 Metabolism, Inborn Errors 714
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors 36
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

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