Term Name:	lysosomal acid lipase deficiency
Synonyms:	LAL deficiency, LAL-D
Definition:	A lipid storage disease characterized by dyslipidemia and accumulation of cholesteryl esters and triglycerides within various organs that has_material_basis_in homozygous or compound heterozygous mutation in the LIPA gene on chromosome 10q23.31.
Ontology:	Human Disease [DOID:0080217]   ( DOID:0080217 )