Sulfatidosis
A group of inherited metabolic disorders characterized by the intralysosomal accumulation of sulfur-containing lipids (SULFATIDES), including SULFOGLYCOSPHINGOLIPIDS normally found in the MYELIN SHEATH of the brain. These disorders are caused by defective degradative enzymes leading to substrate accumulation (or storage).
Year introduced: 2007
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Tree Number(s): C10.228.140.163.100.435.825.850, C16.320.565.189.435.825.850, C16.320.565.398.641.803.925, C16.320.565.595.554.825.850, C18.452.132.100.435.825.850, C18.452.584.563.641.803.925, C18.452.648.189.435.825.850, C18.452.648.398.641.803.925, C18.452.648.595.554.825.850
MeSH Unique ID: D052516
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