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familial hyperalphalipoproteinemia

Benign condition associated with decreased risk of atherosclerosis. Genetics: - autosomal dominant inheritance - associated with CETP deficiency - associated with defects in APOC3 (type 2) [3] Laboratory: elevated HDL cholesterol

Related

cholesteryl ester transfer protein (CETP) deficiency high density lipoprotein (HDL)

General

hyperlipoproteinemia (HLP)

Database Correlations

OMIM correlations

References

  1. Clinical Diagnosis & Management by Laboratory Methods, J.B. Henry (ed), W.B. Saunders Co., Philadelphia, PA. 1991, pg 209
  2. OMIM :accession 143470
  3. OMIM :accession 614028