neutral lipid storage disease Neutral lipid storage disease (NLSD) refers to a group of diseases characterized by a deficit in the degradation of cytoplasmic triglycerides and their accumulation in cytoplasmic lipid vacuoles in most tissues of the body. The group is heterogeneous: currently cases of NLSD with icthyosis (NLSDI/Dorfman-Chanarin disease) and NLSD with myopathy (NLSDM/neutral lipid storage myopathy) can be distinguished. icd11.foundation:621440298 lipidosis with triglycerid storage disease NANDO:1200622 NANDO:2200997 Chanarin-Dorfman syndrome Editor note: DOID:0050729 and wikipedia treat CD-syndrome and NLSD as one, but we follow orphanet is placing CD as a subtype. MEDGEN:1853293 MONDO:0015611 GARD:0003262 DOID:0050729 lipidosis with triglyceride storage disease UMLS:C5848057 Orphanet:165 disorder of phospholipids, sphingolipids and fatty acids biosynthesis lysosomal lipid storage disorder