lysosomal lipid storage disorder
An inherited metabolic disorder in which harmful amounts of lipids accumulate in cells and tissues. Because of a functionally impaired hydrolase or auxiliary protein, their lipid substrates cannot be degraded, accumulate in the lysosome, and slowly spread to other intracellular membranes. [ PMID:21502308 Wikipedia:Lipid_storage_disorder ]
Term info
- Orphanet:79204 (MONDO:equivalentTo)
- DOID:9455 (MONDO:equivalentTo)
- MESH:D008064 (MONDO:equivalentTo)
- UMLS:CN205834 (MONDO:equivalentTo)
- SCTID:10741005 (MONDO:equivalentTo)
- ICD9:272.7 (MONDO:i2s)
- ICD9:272.8 (DOID:9455)
disease_grouping, ordo_group_of_disorders
An inherited metabolic disorder in which harmful amounts of lipids accumulate in cells and tissues. Because of a functionally impaired hydrolase or auxiliary protein, their lipid substrates cannot be degraded, accumulate in the lysosome, and slowly spread to other intracellular membranes.
http://identifiers.org/mesh/D008064, http://linkedlifedata.com/resource/umls/id/CN205834, http://purl.obolibrary.org/obo/DOID_9455, http://identifiers.org/snomedct/10741005, http://purl.obolibrary.org/obo/Orphanet_79204
http://purl.obolibrary.org/obo/MONDO_0019255
lipid storage disease, lipoid storage diseas, inborn lipid storage disorder, lipoid storage disorder, lipoid storage disease, rare inborn error of lipid storage, inborn error of lipid storage
lipoidosis, lipidoses, lipidosis, lipoidoses
MONDO:0019245