Preferred Label : Familial apolipoprotein C-II deficiency;
ICD-11 definition : 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.;
Origin ID : 877401371;
Automatic exact mappings (from CISMeF team)
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.
