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MUCOPOLYSACCHARIDOSES
Descriptors Found:
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DeCS
Descriptor
English
:
Mucopolysaccharidoses
Descriptor
Spanish
:
Mucopolisacaridosis
Descriptor
Portuguese
:
Mucopolissacaridoses
Tree Number:
C16.320.565.202.715
C16.320.565.595.600
C17.300.550.575
C18.452.648.202.715
C18.452.648.595.600
Definition
English
:
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.
Indexing Annotation
English
:
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
History Note
English
:
92; was MUCOPOLYSACCHARIDOSIS 1974-91
Allowable Qualifiers
English
:
BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis
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
RA
radiography
RI
radionuclide imaging
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
US
ultrasonography
UR
urine
VE
veterinary
VI
virology
Record Number:
30388
Unique Identifier:
D009083
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
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