Mucopolysaccharidosis VII
"Mucopolysaccharidosis VII" 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 characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase.
| Descriptor ID |
D016538
|
| MeSH Number(s) |
C16.320.565.202.715.675 C16.320.565.595.600.675 C17.300.550.575.675 C18.452.648.202.715.675 C18.452.648.595.600.675
|
| Concept/Terms |
Mucopolysaccharidosis VII- Mucopolysaccharidosis VII
- Mucopolysaccharidosis VIIs
- VIIs, Mucopolysaccharidosis
- Sly Disease
- Disease, Sly
- beta-Glucuronidase Deficiency
- Deficiencies, beta-Glucuronidase
- Deficiency, beta-Glucuronidase
- beta Glucuronidase Deficiency
- beta-Glucuronidase Deficiencies
- GUSB Deficiency
- Deficiencies, GUSB
- Deficiency, GUSB
- GUSB Deficiencies
- Mucopolysaccharidosis Type VII
- Mucopolysaccharidosis Type VIIs
- Type VII, Mucopolysaccharidosis
- Type VIIs, Mucopolysaccharidosis
- Mucopolysaccharidosis 7
- Sly Syndrome
- Syndrome, Sly
|
Below are MeSH descriptors whose meaning is more general than "Mucopolysaccharidosis VII".
Below are MeSH descriptors whose meaning is more specific than "Mucopolysaccharidosis VII".
This graph shows the total number of publications written about "Mucopolysaccharidosis VII" by people in this website by year, and whether "Mucopolysaccharidosis VII" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Mucopolysaccharidosis VII" by people in Profiles.
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A new case report of severe mucopolysaccharidosis type VII: diagnosis, treatment with haematopoietic cell transplantation and prenatal diagnosis in a second pregnancy. Ital J Pediatr. 2018 Nov 16; 44(Suppl 2):128.