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hypoalphalipoproteinemia, primary, 1

Disease Summary
Associated Targets (2)
Tclin

1

Tbio

1


GARD Rare
Mondo Description Any ypoalphalipoproteinemia in which the cause of the disease is a mutation in the ABCA1 gene.
Uniprot Description Inherited as autosomal dominant trait. It is characterized by moderately low HDL cholesterol, predilection toward premature coronary artery disease (CAD) and a reduction in cellular cholesterol efflux.
Mondo Term and Equivalent IDs
MONDO:0011393:  hypoalphalipoproteinemia, primary, 1
GARD:0002872: