ArcPathVisio
Brace
Octagon
Ellipse
EndoplasmicReticulum
HexagonPathVisio
GolgiApparatus
MimDegradation
Mitochondria
Octagon
PentagonPathVisio
Rectangle
RoundedRectangle
SarcoplasmicReticulum
TrianglePathVisio
none
x
Causes
Liver
Transport
Chylomicron
Familial GPIHBP1 deficiency
Chylomicron remnant
Familial lipase maturation
factor 1 deficiency
ANGPTL8
ANGPTL4
ANGPTL3
Familial lipoprotein lipase deficiency
VLDL
APOA2
APOA4
APOA1
PLTP
Cholesterol
HDL
LDL
Familial apolipoprotein C-II deficiency
LRP1
Familial chylomicronemia
due to inhibition of
lipoprotein lipase
activity
Familial hyperlipidemia
Lipoprotein
IDL
Type I
CETP
LIPC
LCAT
LDLR
Cholesterol
Triglyceride
Phospholipid
GPIHBP1
LPL
APOC2
APOA5
CETP
Binding
Inhibition
Conversion
Gene/protein
Metabolite
Catalysis
Stimulation
Mutations
Legend
x
CETP
LPL
GPIHBP1
LPL
SEL1L
LMF1
Name: Familial hyperlipidemia type 1
Last Modified: 20211130083934
Organism: Homo sapiens