Mucopolysaccharidoses [mukopolysacharidózy]

topical
81
Terms

mukopolysacharidosa
mukopolysacharidosy
mukopolysacharidóza

 

Mucopolysaccharidosis

Persistent link   https://www.medvik.cz/link/D009083
Definition

Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.

Annotation
lysosomal storage dis; types I through VII except V are available as main headings: V = MUCOPOLYSACCHARIDOSIS V see MUCOPOLYSACCHARIDOSIS I; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D009083 MeSH Browser
CUI
M0014167
History note
92; was MUCOPOLYSACCHARIDOSIS 1974-91
Online note
use MUCOPOLYSACCHARIDOSES to search MUCOPOLYSACCHARIDOSIS 1974-91
Public note
92; was MUCOPOLYSACCHARIDOSIS 1974-91

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 10
CO
complications 7
DI
diagnosis 32
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 5
EC
economics 1
EM
embryology
EN
enzymology 1
EP
epidemiology 1
EH
ethnology
ET
etiology 5
GE
genetics 8
HI
history
IM
immunology
ME
metabolism 6
MI
microbiology
MO
mortality 1
NU
nursing
PS
parasitology
PA
pathology 6
PP
physiopathology 9
PC
prevention & control 1
PX
psychology 3
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 27
UR
urine 1
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.565 Metabolism, Inborn Errors 711
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors 36
C16.320.565.202.125 Congenital Disorders of Glycosylation 29
C16.320.565.202.251 Fructose Metabolism, Inborn Errors 5
C16.320.565.202.303 Fucosidosis 2
C16.320.565.202.355 Galactosemias 44
C16.320.565.202.402 Glucosephosphate Dehydrogenase Deficiency 15
C16.320.565.202.449 Glycogen Storage Disease 44
C16.320.565.202.460 Hyperoxaluria, Primary 9
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
C16.320.565.202.715.640 Mucopolysaccharidosis I 29
C16.320.565.202.715.645 Mucopolysaccharidosis II 25
C16.320.565.202.715.650 Mucopolysaccharidosis III 10
C16.320.565.202.715.655 Mucopolysaccharidosis IV 13
C16.320.565.202.715.670 Mucopolysaccharidosis VI 8
C16.320.565.202.715.675 Mucopolysaccharidosis VII 1
C16.320.565.202.720 Multiple Carboxylase Deficiency
C16.320.565.202.810 Pyruvate Metabolism, Inborn Errors 6
C16.320.565.595 Lysosomal Storage Diseases 72
C16.320.565.595.100 Aspartylglucosaminuria
C16.320.565.595.201 Cholesterol Ester Storage Disease 13
C16.320.565.595.377 Cystinosis 16
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System 13
C16.320.565.595.577 Mannosidase Deficiency Diseases 1
C16.320.565.595.600 Mucopolysaccharidoses 81
C16.320.565.595.600.640 Mucopolysaccharidosis I 29
C16.320.565.595.600.645 Mucopolysaccharidosis II 25
C16.320.565.595.600.650 Mucopolysaccharidosis III 10
C16.320.565.595.600.655 Mucopolysaccharidosis IV 13
C16.320.565.595.600.670 Mucopolysaccharidosis VI 8
C16.320.565.595.600.675 Mucopolysaccharidosis VII 1
C16.320.565.595.800 Pycnodysostosis 2
C17 Skin and Connective Tissue Diseases 32
C17.300 Connective Tissue Diseases 281
C17.300.550 Mucinoses 17
C17.300.550.274 Ganglion Cysts 12
C17.300.550.550 Mucinosis, Follicular 9
C17.300.550.575 Mucopolysaccharidoses 81
C17.300.550.575.640 Mucopolysaccharidosis I 29
C17.300.550.575.645 Mucopolysaccharidosis II 25
C17.300.550.575.650 Mucopolysaccharidosis III 10
C17.300.550.575.655 Mucopolysaccharidosis IV 13
C17.300.550.575.670 Mucopolysaccharidosis VI 8
C17.300.550.575.675 Mucopolysaccharidosis VII 1
C17.300.550.590 Myxedema 41
C17.300.550.750 Scleredema Adultorum 8
C17.300.550.875 Scleromyxedema 15
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
C18.452.648.202.125 Congenital Disorders of Glycosylation 29
C18.452.648.202.251 Fructose Metabolism, Inborn Errors 5
C18.452.648.202.303 Fucosidosis 2
C18.452.648.202.355 Galactosemias 44
C18.452.648.202.402 Glucosephosphate Dehydrogenase Deficiency 15
C18.452.648.202.449 Glycogen Storage Disease 44
C18.452.648.202.460 Hyperoxaluria, Primary 9
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
C18.452.648.202.715.640 Mucopolysaccharidosis I 29
C18.452.648.202.715.645 Mucopolysaccharidosis II 25
C18.452.648.202.715.650 Mucopolysaccharidosis III 10
C18.452.648.202.715.655 Mucopolysaccharidosis IV 13
C18.452.648.202.715.670 Mucopolysaccharidosis VI 8
C18.452.648.202.715.675 Mucopolysaccharidosis VII 1
C18.452.648.202.720 Multiple Carboxylase Deficiency
C18.452.648.202.810 Pyruvate Metabolism, Inborn Errors 6
C18.452.648.595 Lysosomal Storage Diseases 72
C18.452.648.595.100 Aspartylglucosaminuria
C18.452.648.595.201 Cholesterol Ester Storage Disease 13
C18.452.648.595.377 Cystinosis 16
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System 13
C18.452.648.595.577 Mannosidase Deficiency Diseases 1
C18.452.648.595.600 Mucopolysaccharidoses 81
C18.452.648.595.600.640 Mucopolysaccharidosis I 29
C18.452.648.595.600.645 Mucopolysaccharidosis II 25
C18.452.648.595.600.650 Mucopolysaccharidosis III 10
C18.452.648.595.600.655 Mucopolysaccharidosis IV 13
C18.452.648.595.600.670 Mucopolysaccharidosis VI 8
C18.452.648.595.600.675 Mucopolysaccharidosis VII 1
C18.452.648.595.800 Pycnodysostosis 2

Hyaluronidase Deficiency Disease MeSH Browser

Mucopolysaccharidoses, Unclassified Types Disease MeSH Browser

Mucopolysaccharidosis Type VIII Disease MeSH Browser

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