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MANNOSIDASE DEFICIENCY DISEASES
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DeCS
Descriptor
English
:
Mannosidase Deficiency Diseases
Descriptor
Spanish
:
Enfermedades por Deficiencia de Manosidasa
Descriptor
Portuguese
:
Doenças por Deficiência de Manosidase
Synonyms
English
:
Mannosidosis
Tree Number:
C16.320.565.202.607
C16.320.565.595.577
C18.452.648.202.607
C18.452.648.595.577
Definition
English
:
Diseases caused by the loss of one or more
enzymes
involved in the
hydrolysis
of mannoside linkages (
MANNOSIDASES
). The defects in enzyme activity are primarily associated with genetic
mutation
of the
genes
that
codes
for a particular mannosidase isoenzyme.
See Related
English
:
Mannosidases
History Note
English
:
2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003
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:
38053
Unique Identifier:
D044904
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
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