Multiple Sulfatase Deficiency Disease
"Multiple Sulfatase Deficiency Disease" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An inherited metabolic disorder characterized by the intralysosomal accumulation of sulfur-containing lipids (sulfatides) and MUCOPOLYSACCHARIDES. Excess levels of both substrates are present in urine. This is a disorder of multiple sulfatase (arylsulfatases A, B, and C) deficiency which is caused by the mutation of sulfatase-modifying factor-1. Neurological deterioration is rapid.
| Descriptor ID |
D052517
|
| MeSH Number(s) |
C10.228.140.163.100.435.825.850.750 C16.320.565.189.435.825.850.750 C16.320.565.398.641.803.925.750 C16.320.565.595.554.825.850.750 C18.452.132.100.435.825.850.750 C18.452.584.687.803.925.750 C18.452.648.189.435.825.850.750 C18.452.648.398.641.803.925.750 C18.452.648.595.554.825.850.750
|
| Concept/Terms |
Multiple Sulfatase Deficiency Disease- Multiple Sulfatase Deficiency Disease
- Multiple Sulfatase Deficiency
- Multiple Sulfatase Deficiencies
- Multiple Sulphatase Deficiency Disease
- Mucosulfatidosis
Sulfatidosis, Juvenile, Austin Type- Sulfatidosis, Juvenile, Austin Type
- Sulfatidosis Juvenile, Austin Type
- Juvenile Sulfatidosis
- Juvenile Sulfatidoses
- Sulfatidoses, Juvenile
- Sulfatidosis, Juvenile
|
Below are MeSH descriptors whose meaning is more general than "Multiple Sulfatase Deficiency Disease".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Brain Diseases [C10.228.140]
- Brain Diseases, Metabolic [C10.228.140.163]
- Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
- Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
- Sphingolipidoses [C10.228.140.163.100.435.825]
- Sulfatidosis [C10.228.140.163.100.435.825.850]
- Multiple Sulfatase Deficiency Disease [C10.228.140.163.100.435.825.850.750]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Metabolism, Inborn Errors [C16.320.565]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
- Sphingolipidoses [C16.320.565.189.435.825]
- Sulfatidosis [C16.320.565.189.435.825.850]
- Multiple Sulfatase Deficiency Disease [C16.320.565.189.435.825.850.750]
- Lipid Metabolism, Inborn Errors [C16.320.565.398]
- Lipidoses [C16.320.565.398.641]
- Sphingolipidoses [C16.320.565.398.641.803]
- Sulfatidosis [C16.320.565.398.641.803.925]
- Multiple Sulfatase Deficiency Disease [C16.320.565.398.641.803.925.750]
- Lysosomal Storage Diseases [C16.320.565.595]
- Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
- Sphingolipidoses [C16.320.565.595.554.825]
- Sulfatidosis [C16.320.565.595.554.825.850]
- Multiple Sulfatase Deficiency Disease [C16.320.565.595.554.825.850.750]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
- Sphingolipidoses [C18.452.132.100.435.825]
- Sulfatidosis [C18.452.132.100.435.825.850]
- Multiple Sulfatase Deficiency Disease [C18.452.132.100.435.825.850.750]
- Lipid Metabolism Disorders [C18.452.584]
- Lipidoses [C18.452.584.687]
- Sphingolipidoses [C18.452.584.687.803]
- Sulfatidosis [C18.452.584.687.803.925]
- Multiple Sulfatase Deficiency Disease [C18.452.584.687.803.925.750]
- Metabolism, Inborn Errors [C18.452.648]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
- Sphingolipidoses [C18.452.648.189.435.825]
- Sulfatidosis [C18.452.648.189.435.825.850]
- Multiple Sulfatase Deficiency Disease [C18.452.648.189.435.825.850.750]
- Lipid Metabolism, Inborn Errors [C18.452.648.398]
- Lipidoses [C18.452.648.398.641]
- Sphingolipidoses [C18.452.648.398.641.803]
- Sulfatidosis [C18.452.648.398.641.803.925]
- Multiple Sulfatase Deficiency Disease [C18.452.648.398.641.803.925.750]
- Lysosomal Storage Diseases [C18.452.648.595]
- Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
- Sphingolipidoses [C18.452.648.595.554.825]
- Sulfatidosis [C18.452.648.595.554.825.850]
- Multiple Sulfatase Deficiency Disease [C18.452.648.595.554.825.850.750]
Below are MeSH descriptors whose meaning is more specific than "Multiple Sulfatase Deficiency Disease".
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