familial lipase maturation factor 1 deficiency

Summary
Synonym
  • LPL and HL deficiency
  • LPL and HTGL deficiency
  • combined lipase deficiency
  • familial LMF1 deficiency
  • lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency
Definition
A familial chylomicronemia syndrome characterized by hypertriglyceridemia, chylomicronemia, and decreased lipase activity that has_material_basis_in homozygous mutation in the LMF1 gene on chromosome 16p13.3.
Super Class
autosomal recessive disease familial chylomicronemia syndrome
Disease Ontology
DOID:0111422
Mondo Disease Ontology
ORDO
OMIM
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
64788 LMF1 lipase maturation factor 1

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024