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Hyperlipemia

Hyperlipemia is a lipid disorder characterized by elevated cholesterol and/or triglyceride levels.

Systematic

Dyslipidemia
Apolipoprotein deficiency
Betalipoprotein deficiency
Epigenetic dyslipidemia
Hyperalphalipoproteinemia 1
Hyperalphalipoproteinemia 2
Hyperlipemia
Chylomicronemia
ABCA1
ABCG5
APOA5
APOC2
APOE
Chylomicron retention disease
SAR1B
GPIHBP1
LCAT
LIPA
LIPC
LMF1
LPL
SAR1B
Familial combined Hyperlipemia
Combined familial hyperlipidemia with VLDL overproduction
APOE
GCKR
OSBPL10
USF1
Combined familial hyperlipidemia with adipose tissue dysfunction
C5AR2
CREB3L3
LEPR
LIPE
PNPLA2
PPARG
USF1
Combined familial hyperlipidemia with dysfunctional LDL clearance
ATF6
LDLR
PCSK9
Combined familial hyperlipidemia with dysfunctional VLDL metabolism
ANGPTL8
APOA1
APOA4
APOA5
APOC3
CETP
GALNT2
LCAT
LIPC
LIPG
LPL
RXRG
USF1
Hypercholesterolemia
Autosomal dominant hypercholesterolemia 1
LDLR
Autosomal dominant hypercholesterolemia 2
APOB
Autosomal dominant hypercholesterolemia 3
PCSK9
Autosomal recessive hypercholesterolemia
LDLRAP1
Low density lipoprotein cholesterol level quantitative trait locus
HMGCR
Lp(a) hyperlipoproteinemia
LPA
Hypertriglyceridemia
APOA5
APOE
Combined lipase deficiency
LMF1
GPIHBP1
LIPC
LIPE
LPL
Plasma triglyceride level quantitative trait locus
ANGPTL4
Transient infantile hypertriglyceridemia
GPD1
Lysosomal acid lipase deficiency
LIPA
Hypoalphalipoproteinemia
Hypobetalipoproteinemia

References:

1.

Hayden MR et al. (1987) DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemias.

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2.

Beratis NG et al. (1976) Alkaline phosphatase activity in cultured skin fibroblasts from fibrodysplasia ossificans progressiva.

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3.

Cohen RB et al. (1993) The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients.

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4.

Connor JM et al. (1993) A three generation family with fibrodysplasia ossificans progressiva.

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5.

Kaplan FS et al. (1993) Genetic transmission of fibrodysplasia ossificans progressiva. Report of a family.

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6.

Kaplan FS et al. (1993) The histopathology of fibrodysplasia ossificans progressiva. An endochondral process.

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7.

Schroeder HW et al. (1980) The hand and foot malformations in fibrodysplasia ossificans progressiva.

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8.

Connor JM et al. (1982) Genetic aspects of fibrodysplasia ossificans progressiva.

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9.

Tünte W et al. (1967) [On the genetics of myositis ossificans progressiva].

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10.

Rogers JG et al. (1979) Paternal age effect in fibrodysplasia ossificans progressiva.

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11.

Kaplan FS et al. (2008) Response to "Mutations of the NOGGIN and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al.

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12.

Seemann P et al. (2008) The tale of FOP, NOGGIN and myristoylation: no data, no proof!

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13.

Kitterman JA et al. (2005) Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva.

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14.

de la Peña LS et al. (2005) Fibrodysplasia ossificans progressiva (FOP), a disorder of ectopic osteogenesis, misregulates cell surface expression and trafficking of BMPRIA.

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15.

Daltroff G et al. (1992) [Fibromatosis and fibrodysplasia ossificans progressiva. An avoidable diagnostic error].

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16.

Maxwell WA et al. (1977) Histochemical and ultrastructural studies in fibrodysplasia ossificans progressiva (myositis ossificans progressiva).

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17.

Lucotte G et al. (2000) Localization of the gene for fibrodysplasia ossificans progressiva (FOP) to chromosome 17q21-22.

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18.

Allayee H et al. (2003) Biochemical and genetic association of plasma apolipoprotein A-II levels with familial combined hyperlipidemia.

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19.

Steingrímsson E et al. (1995) Murine chromosomal location of five bHLH-Zip transcription factor genes.

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20.

Viollet B et al. (1996) Immunochemical characterization and transacting properties of upstream stimulatory factor isoforms.

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21.

Ye M et al. (1993) The secretion of fluid by renal cysts from patients with autosomal dominant polycystic kidney disease.

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22.

None (1969) Polycythemia resulting from abnormal hemoglobins.

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23.

WITHERSPOON FG et al. (1948) Familial urticaria due to cold.

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24.

Siegel AM et al. (2005) Adult-onset epilepsy in focal cortical dysplasia of Taylor type.

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25.

DORMANDY TL et al. (1961) Familial fructose and galactose intolerance.

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26.

SAMOLS E et al. (1963) Insulin response to fructose and galactose.

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27.

Turner RC et al. (1972) Familial fructose and galactose intolerance.

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28.

Feldman G et al. (2000) Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31.

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29.

Rogers JG et al. (1979) Fibrodysplasia ossificans progressiva. A survey of forty-two cases.

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30.

OMIM.ORG article

Omim 229500 external link
31.

OMIM.ORG article

Omim 135100 external link
32.

OMIM.ORG article

Omim 612781 external link
33.

Wikipedia article

Wikipedia EN (Food_intolerance) external link
Update: Aug. 14, 2020
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