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GANGLIOSIDE STORAGE DISORDER
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DeCS
Descriptor
English
:
Gangliosidoses
Descriptor
Spanish
:
Gangliosidosis
Descriptor
Portuguese
:
Gangliosidoses
Synonyms
English
:
Ganglioside Storage Diseases
Ganglioside Storage Disorders
Gangliosidosis
Ganglioside Storage Disease
Ganglioside Storage Disorder
Storage Disease, Ganglioside
Storage Diseases, Ganglioside
Storage Disorder, Ganglioside
Storage Disorders, Ganglioside
Tree Number:
C10.228.140.163.100.435.825.300
C16.320.565.189.435.825.300
C16.320.565.398.641.803.350
C16.320.565.595.554.825.300
C18.452.132.100.435.825.300
C18.452.584.687.803.350
C18.452.648.189.435.825.300
C18.452.648.398.641.803.350
C18.452.648.595.554.825.300
Definition
English
:
A group of autosomal recessive lysosomal storage disorders marked by the accumulation of
GANGLIOSIDES
. They are caused by impaired
enzymes
or defective cofactors required for normal ganglioside degradation in the
LYSOSOMES
.
Gangliosidoses
are classified by the specific ganglioside accumulated in the defective degradation pathway.
Indexing Annotation
English
:
coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and
GANGLIOSIDOSES
, GM2 are available
See Related
English
:
Mucolipidoses
History Note
English
:
1992(1976)
Allowable Qualifiers
English
:
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
Record Number:
30336
Unique Identifier:
D005733
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
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