Hypoalphalipoproteinemia

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Hypoalphalipoproteinemia
Classification and external resources
ICD-10 E78.6
ICD-9 272.5
OMIM 604091
eMedicine med/3368 
MeSH D052456

Hypoalphalipoproteinemia is a high-density lipoprotein deficiency, inherited in an autosomal dominant manner.[1]

Hypoalphalipoproteinemia has an autosomal dominant pattern of inheritance.
Hypoalphalipoproteinemia has an autosomal dominant pattern of inheritance.

It can be associated with LDL receptor.[2]

[edit] References

  1. ^ Online 'Mendelian Inheritance in Man' (OMIM) 604091
  2. ^ Pisciotta L, Calabresi L, Lupattelli G, et al (September 2005). "Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes". Atherosclerosis 182 (1): 153–9. doi:10.1016/j.atherosclerosis.2005.01.048. PMID 16115486. 
v • d • e
Lipid metabolism disorders / Inborn error of lipid metabolism - dyslipidemia (E78 and E71.3, 272)
Hyperlipidemia
Hypolipoproteinemia
Lipodystrophy
Fatty acid metabolism deficiency
Cholesterol synthesis
Other


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