|
Lipoprotein lipase
deficiency |
OMIM:238600 |
|
|
Apolipoprotein C-II
deficiency |
OMIM:207750 |
|
|
Familial
dysbetalipoproteinemia (FD) |
OMIM:107741 |
|
|
Hepatic lipase
deficiency |
OMIM:151670 |
|
|
Hypercholesterolémie
familiární, homozygotní forma |
Familial
hypercholesterolemia (FH) homozygous |
OMIM:143890 |
|
Hypercholesterolémie
familiární, heterozygotní forma |
Familial
hypercholesterolemia (FH) heterozygous |
OMIM:143890 |
|
Familiární defekt apolipoproteinu B100 |
Defective
apolipoprotein B-100 |
OMIM:107730 |
|
Apolipoprotein A-I
deficiency (familial) |
OMIM:107680 |
|
|
Apolipoprotein A-I
deficiency (struktural mutations) |
OMIM:107680 |
|
|
Alfa-an-lipoproteinémie
(Tangierská nemoc) |
Tangier disease |
OMIM:205400 |
|
LCAT deficiency
(complete) |
OMIM:2454900 |
|
|
LCAT deficiency
(partial) |
OMIM:2454900 |
|
|
Abetalipoproteinemia |
OMIM:200100 |
|
|
(homozygotní forma) |
Hypobetalipoproteinemia
(homozygous) |
OMIM:107730 |
|
(heterozygotní
forma) |
Hypobetalipoproteinemia
(heterozygous) |
OMIM:107730 |