Orphanet: Familial lipoprotein lipase deficiency

Search for a rare disease

* (*) mandatory field

Other search option(s)

Suggest an update

(*) Required fields.


Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image

Familial lipoprotein lipase deficiency


Classification level: Subtype of disorder
  • Synonym(s):
    • LPL deficiency
  • Prevalence: 1-9 / 1 000 000
  • Inheritance: -
  • Age of onset: Infancy, Childhood
  • ICD-10: E78.3
  • OMIM: 144250  238600
  • UMLS: C0023817
  • MeSH: -
  • GARD: 12241
  • MedDRA: -

Detailed information


The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.