Search on: HYPERLIPOPROTEINEMIA TYPE I 
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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:
 

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