Apolipoprotein C2 deficiency

Synonym(s)
- APOC2-related familial Hyperchylomicronemia,
- Hyperlipoproteinemia type 1B
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- APOC2 / Apolipoprotein C2
  19q13.32
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Apolipoprotein C2
Disease group(s)
- 15.2 Hypertriglyceridemias