ArcPathVisio
Brace
Octagon
Ellipse
EndoplasmicReticulum
HexagonPathVisio
GolgiApparatus
MimDegradation
Mitochondria
Octagon
PentagonPathVisio
Rectangle
RoundedRectangle
SarcoplasmicReticulum
TrianglePathVisio
none
Norum disease
Abetalipoproteinemia
Alcohol
Diabetes mellitus
Malabsorption
Malnutrition
Caused by
Tangier disease
Cancer
Familial hypobetalipoproteinemia
Hypothyroidism
Endocrine/metabolic disorders
Hyperthyroidism
Drugs
Nephrotic syndrome
Kidney failure
Familial GPIHBP1 deficiency
Chronic infections
Familial combined hypolipidemia
Familial lipase maturation factor 1 deficiency
Caused by
Hyperlipidemia
Progeria Associated Lipodystrophy
Congenital Generalized Lipodystrophy
(CGL)
Type IV
Hypolipoproteinemia
Familial Partial Lipodystrophy
(FPLD)
Dyslipidemia
Type I
Lipodystrophy
Type III
Acquired Partial Lipodystrophy
Type II
Adipose levels
Decreased levels
Autoinflammatory lipodystrophy
Within blood
Within adipocytes
HIV-associated Lipodystrophy
Increased levels
Acquired Generalized Lipodystrophy
Acquired
Acquired
Familial / Congenital
Familial Combined Hyperlipidemia
Familial Hypertriglyceridemia
Familial Hypercholesterolemia
Familial Dysbetalipoproteinemia
Familial chylomicronemia due to LPL inhibition
Familial apoprotein CII deficiency
Familial Hyperchylomicronemia
Mixed hyperlipidemia
Familial / Congenital
CGL4
CGL3
CGL1
CGL2
FPLD6
FPLD5
FPLD2
FPLD3
FPLD4
FPLD1
Acquired
Familial / Congenital
Type V
Familial hypobetalipoproteinemia type 1
Familial hypobetalipoproteinemia type 2
Name: Meta pathway lipodystrophy, dyslipidemia and hyperlipidemia
Last Modified: 20230131214626
Organism: Homo sapiens