Congenital Disorder

Hypoalphalipoproteinemias

AMW:DIS:160117

Conditions with abnormally low levels of ALPHA-LIPOPROTEINS (high-density lipoproteins) in the blood. Hypoalphalipoproteinemia can be associated with mutations in genes encoding APOLIPOPROTEIN A-I; LECITHIN CHOLESTEROL ACYLTRANSFERASE; and ATP-BINDING CASSETTE TRANSPORTERS.

Pathology clinical

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Tangier Disease has parent Hypoalphalipoproteinemias

Lecithin Cholesterol Acyltransferase Deficiency has parent Hypoalphalipoproteinemias

Hypoalphalipoproteinemias has parent Hypolipoproteinemias

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