Catalog

Familial apolipoprotein C-II deficiency

No MMS code

Link to WHO Definition

Familial apolipoprotein C-II deficiency – http://id.who.int/icd/entity/877401371

This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons.