disease caused by disruption of disease has basis in disruption of sphingolipid metabolic process lysosomal lipid storage disorder sphingolipidosis An inherited metabolic disorder that affects the lysosomal degradation of the spinhgolipids. Representative examples include Gaucher disease, Tay-Sachs disease, and Niemann-Pick disease. DOID:1927 GARD:0007672 ICD10:E75.0 ICD10:E75.1 ICD10:E75.2 ICD10:E75.3 MESH:D013106 MONDO:0019255 NCIT:C117254 Orphanet:79225 SCTID:238028008 UMLS:C0037899 https://rarediseases.info.nih.gov/diseases/7672/sphingolipidosis sphingolipidoses sphingolipidosis, NOS