Hypoalphalipoproteinemia, primary, 1

MONDO:0011393

Any ypoalphalipoproteinemia in which the cause of the disease is a mutation in the ABCA1 gene.

Also known as: HDL deficiency, familial, 1, hypoalphalipoproteinemia, familial, FHA, FHD, HDL cholesterol, Low serum, HDLD, familial HDL deficiency, high density lipoprotein deficiency

26 clinical trials for this condition and its sub-types.

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