"Mucopolysaccharidosis VI" 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.
Mucopolysaccharidosis with excessive CHONDROITIN SULFATE B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-ACETYLGALACTOSAMINE-4-SULFATASE (arylsulfatase B).
| Descriptor ID |
D009087
|
| MeSH Number(s) |
C16.320.565.202.715.670 C16.320.565.595.600.670 C17.300.550.575.670 C18.452.648.202.715.670 C18.452.648.595.600.670
|
| Concept/Terms |
Mucopolysaccharidosis VI- Mucopolysaccharidosis VI
- Arylsulfatase B Deficiency
- Arylsulfatase B Deficiencies
- Deficiencies, Arylsulfatase B
- Deficiency, Arylsulfatase B
- Maroteaux-Lamy Syndrome
- Maroteaux Lamy Syndrome
- Syndrome, Maroteaux-Lamy
- Mucopolysaccharidosis Type VI
- Type VI, Mucopolysaccharidosis
- Mucopolysaccharidosis Type 6
- Type 6, Mucopolysaccharidosis
- N-Acetylgalactosamine-4-Sulfatase Deficiency
- Deficiencies, N-Acetylgalactosamine-4-Sulfatase
- Deficiency, N-Acetylgalactosamine-4-Sulfatase
- N-Acetylgalactosamine-4-Sulfatase Deficiencies
- Polydystrophic Dwarfism
- Dwarfism, Polydystrophic
- ARSB Deficiency
- ARSB Deficiencies
- Deficiencies, ARSB
- Deficiency, ARSB
- Mucopolysaccharidosis 6
|
Below are MeSH descriptors whose meaning is more general than "Mucopolysaccharidosis VI".
Below are MeSH descriptors whose meaning is more specific than "Mucopolysaccharidosis VI".
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