Lecithin:cholesterol acyltransferase deficiency

Synonym(s)
- Norum disease
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- LCAT / Lecithin Cholesterol Acyltransferase
  16q22.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Lecithin-cholesterol acyltransferase
Disease group(s)
- 15.4 Disorders of high-density lipoprotein (HDL) metabolism
Child entries
- Fish-eye disease
- Lecithin:cholesterol acyltransferase deficiency, familial