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 0
CF
cerebrospinal fluid 0
CI
chemically induced 0
CL
classification 0
CO
complications 0
DI
diagnosis 0
DG
diagnostic imaging 0
DH
diet therapy 0
DT
drug therapy 0
EC
economics 0
EM
embryology 0
EN
enzymology 0
EP
epidemiology 0
EH
ethnology 0
ET
etiology 0
GE
genetics 0
HI
history 0
IM
immunology 0
ME
metabolism 0
MI
microbiology 0
MO
mortality 0
NU
nursing 0
PS
parasitology 0
PA
pathology 0
PP
physiopathology 0
PC
prevention & control 0
PX
psychology 0
RT
radiotherapy 0
RH
rehabilitation 0
SU
surgery 0
TH
therapy 0
UR
urine 0
VE
veterinary 0
VI
virology 0

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 212
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 171
C18.452 Metabolic Diseases 1 192
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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