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Sulfatidosis MeSH Descriptor Data 2023


MeSH Heading
Sulfatidosis
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
Unique ID
D052516
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D052516
Scope Note
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).
Public MeSH Note
2007; see LEUKODYSTROPHY, METACHROMATIC 1974-2006
History Note
2007; use LEUKODYSTROPHY, METACHROMATIC 1974-2006
Date Established
2007/01/01
Date of Entry
2006/07/05
Revision Date
2021/07/01
Sulfatidosis Preferred
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