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HYPERCHYLOMICRONEMIA, FAMILIAL
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DeCS
Descriptor
English
:
Hyperlipoproteinemia Type I
Descriptor
Spanish
:
Hiperlipoproteinemia Tipo I
Descriptor
Portuguese
:
Hiperlipoproteinemia Tipo I
Synonyms
English
:
Apolipoprotein C-II Deficiency
Hyperchylomicronemia, Familial
Lipoprotein Lipase Deficiency, Familial
Tree Number:
C16.320.565.398.465
C18.452.584.500.500.644.237
C18.452.648.398.465
Definition
English
:
An inherited condition due to a deficiency of either
LIPOPROTEIN LIPASE
or
APOLIPOPROTEIN C-II
(a lipase-activating protein). The lack of
lipase
activities results in inability to remove
CHYLOMICRONS
and
TRIGLYCERIDES
from the
blood
which has a creamy top layer after standing.
See Related
English
:
Apolipoprotein C-II
Lipoprotein Lipase
History Note
English
:
2007 (1980)
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:
8246
Unique Identifier:
D008072
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
LIS