Diseases

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).

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

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).

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MeSH Record

Synonyms

1 entry terms
  • Sulfatidoses

MeSH Record

Aspects Covered

34 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

History Note

2007; use LEUKODYSTROPHY, METACHROMATIC 1974-2006

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References

  1. National Library of Medicine. Sulfatidosis. Medical Subject Headings (MeSH). 2026. Unique ID D052516. http://id.nlm.nih.gov/mesh/2026/D052516
  2. Sulfatidosis. In: Wikipedia. https://en.wikipedia.org/wiki/Sulfatidosis
  3. Sulfatidosis. In: Wikidata. https://www.wikidata.org/wiki/Q7636192