Hyperlipoproteinemia Type I [hyperlipoproteinemie typ I]

topical
21
Terms

apolipoprotein C-II - nedostatek
Burger-Grutzova nemoc
deficit apolipoproteinu C-II
familiární deficit lipoproteinové lipázy
familiární deficit LPL
familiární hyperchylomikronemie
familiární hyperlipoproteinemie typ I
hyperchylomikronémie familiární
hyperlipoproteinémie typ I
hyperlipoproteinemie typ Ia
hyperlipoproteinemie typ Ib
hyperlipoproteinémie typ Ib
LLD
LPLD
nedostatek apolipoproteinu C-II

 

Apolipoprotein C-II Deficiency
Burger-Grutz Syndrome
C-II Anapolipoproteinemia
Chylomicronemia, Familial
Familial Fat-Induced Hypertriglyceridemia
Familial Hyperchylomicronemia
Familial Hyperlipoproteinemia Type 1
Familial Lipoprotein Lipase Deficiency
Familial LPL Deficiency
Hyperchylomicronemia, Familial
Hyperlipemia, Essential Familial
Hyperlipemia, Idiopathic, Burger-Grutz Type
Hyperlipoproteinemia Type Ia
Hyperlipoproteinemia Type Ib
Hyperlipoproteinemia, Type I
Hyperlipoproteinemia, Type Ia
Hyperlipoproteinemia, Type Ib
Lipase D Deficiency
LIPD Deficiency
Lipoprotein Lipase Deficiency
Lipoprotein Lipase Deficiency, Familial

Persistent link   https://www.medvik.cz/link/D008072
Definition

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.

DUI
D008072 MeSH Browser
CUI
M0012579
Previous indexing
Hyperlipidemia/familial & genetic (1966-1979)
History note
2007 (1980)
Public note
2007; see LIPOPROTEIN LIPASE DEFICIENCY, FAMILIAL 1991-2006, see HYPERLIPOPROTEINEMIA 1980-1990

Allowable subheadings

BL
blood 1
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 3
DI
diagnosis 11
DG
diagnostic imaging
DH
diet therapy 2
DT
drug therapy 3
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 2
GE
genetics 8
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
PP
physiopathology 1
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 8
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.565 Metabolism, Inborn Errors 714
C16.320.565.398 Lipid Metabolism, Inborn Errors 154
C16.320.565.398.224 Barth Syndrome 6
C16.320.565.398.450 Hyperlipidemia, Familial Combined 68
C16.320.565.398.465 Hyperlipoproteinemia Type I 21
C16.320.565.398.481 Hyperlipoproteinemia Type II 456
C16.320.565.398.483 Hyperlipoproteinemia Type III 19
C16.320.565.398.487 Hyperlipoproteinemia Type IV 14
C16.320.565.398.493 Hyperlipoproteinemia Type V 6
C16.320.565.398.500 Hypolipoproteinemias 35
C16.320.565.398.641 Lipidoses 35
C16.320.565.398.745 Lipodystrophy, Congenital Generalized 1
C16.320.565.398.850 Smith-Lemli-Opitz Syndrome 30
C16.320.565.398.925 Xanthomatosis, Cerebrotendinous
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 200
C18.452.584 Lipid Metabolism Disorders 99
C18.452.584.500 Dyslipidemias 1 652
C18.452.584.500.500 Hyperlipidemias 1 238
C18.452.584.500.500.644 Hyperlipoproteinemias 771
C18.452.584.500.500.644.237 Hyperlipoproteinemia Type I 21
C18.452.584.500.500.644.475 Hyperlipoproteinemia Type II 456
C18.452.584.500.500.644.485 Hyperlipoproteinemia Type III 19
C18.452.584.500.500.644.490 Hyperlipoproteinemia Type IV 14
C18.452.584.500.500.644.495 Hyperlipoproteinemia Type V 6
C18.452.584.563 Lipid Metabolism, Inborn Errors 154
C18.452.584.563.224 Barth Syndrome 6
C18.452.584.563.450 Hyperlipidemia, Familial Combined 68
C18.452.584.563.465 Hyperlipoproteinemia Type I 21
C18.452.584.563.481 Hyperlipoproteinemia Type II 456
C18.452.584.563.483 Hyperlipoproteinemia Type III 19
C18.452.584.563.487 Hyperlipoproteinemia Type IV 14
C18.452.584.563.493 Hyperlipoproteinemia Type V 6
C18.452.584.563.497 Hypobetalipoproteinemia, Familial, Apolipoprotein B 1
C18.452.584.563.500 Hypolipoproteinemias 35
C18.452.584.563.641 Lipidoses 35
C18.452.584.563.745 Lipodystrophy, Congenital Generalized 1
C18.452.584.563.798 Lipodystrophy, Familial Partial 1
C18.452.584.563.824 Shwachman-Diamond Syndrome 2
C18.452.584.563.850 Smith-Lemli-Opitz Syndrome 30
C18.452.584.563.925 Xanthomatosis, Cerebrotendinous
C18.452.648 Metabolism, Inborn Errors 714
C18.452.648.398 Lipid Metabolism, Inborn Errors 154
C18.452.648.398.224 Barth Syndrome 6
C18.452.648.398.450 Hyperlipidemia, Familial Combined 68
C18.452.648.398.465 Hyperlipoproteinemia Type I 21
C18.452.648.398.481 Hyperlipoproteinemia Type II 456
C18.452.648.398.483 Hyperlipoproteinemia Type III 19
C18.452.648.398.487 Hyperlipoproteinemia Type IV 14
C18.452.648.398.493 Hyperlipoproteinemia Type V 6
C18.452.648.398.500 Hypolipoproteinemias 35
C18.452.648.398.641 Lipidoses 35
C18.452.648.398.745 Lipodystrophy, Congenital Generalized 1
C18.452.648.398.850 Smith-Lemli-Opitz Syndrome 30
C18.452.648.398.925 Xanthomatosis, Cerebrotendinous

Familial hyperchylomicronemia syndrome Disease MeSH Browser

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