Hypoalphalipoproteinemia, primary, 1

Definition

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 — per MONDO

Also identified as

• DOID 0080957 per MONDO
• OMIM 604091 per MONDO
• UMLS C5231558 per MONDO