Wolman disease

Summary
Synonym
  • Acid esterase deficiency
  • Acid lipase deficiency
  • Wolman xanthomatosis
  • Wolman's disease
  • Wolman's or triglyceride storage type III disease
  • Xanthomatosis, familial
  • acute infantile lysosomal acid lipase deficiency
  • complete LAL deficiency
  • complete LIPA deficiency
  • complete cholesterol ester hydrolase deficiency
  • complete lysosomal acid lipase deficiency
Definition
A lysosomal acid lipase deficiency characterized by infantile onset of rapidly progressive accumulation of cholesteryl esters and triglycerides throughout the body, resulting in hepatosplenomegaly, severe malnutrition, jaundice, vomiting, diarrhea, steatorrhea. Death usually occurs within the first year of life.
Super Class
lysosomal acid lipase deficiency
External Links
Disease Ontology
DOID:14497
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 18 of 18 in total
Gene ID Gene Symbol Description Source
4684 NCAM1 neural cell adhesion molecule 1
6319 SCD stearoyl-CoA desaturase
6441 SFTPD surfactant protein D
6515 SLC2A3 solute carrier family 2 member 3
8435 SOAT2 sterol O-acyltransferase 2
8513 LIPF lipase F, gastric type
9415 FADS2 fatty acid desaturase 2
79153 GDPD3 glycerophosphodiester phosphodiesterase domain containing 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
16889 Lipa lysosomal acid lipase A

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Last updated: August 19, 2024