Primary hypoalphalipoproteinemia

Primary hypoalphalipoproteinemia
ICD-10	E78.6
ICD-9	272.5
OMIM	604091
eMedicine	med/3368
MeSH	D052456

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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

Primary hypoalphalipoproteinemia has an autosomal dominant pattern of inheritance.

It can be associated with LDL receptor.

References

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