| Descriptor English: | Mucopolysaccharidosis VII | ||||||
| Descriptor Spanish: |
Mucopolisacaridosis VII
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| Descriptor Portuguese: | Mucopolissacaridose VII | ||||||
| Descriptor French: | Mucopolysaccharidose de type VII | ||||||
| Entry term(s): |
Deficiencies, GUSB Deficiencies, beta-Glucuronidase Deficiency, GUSB Deficiency, beta-Glucuronidase Disease, Sly GUSB Deficiencies GUSB Deficiency Mucopolysaccharidosis 7 Mucopolysaccharidosis Type VII Mucopolysaccharidosis Type VIIs Mucopolysaccharidosis VIIs Sly Disease Sly Syndrome Syndrome, Sly Type VII, Mucopolysaccharidosis Type VIIs, Mucopolysaccharidosis VIIs, Mucopolysaccharidosis beta Glucuronidase Deficiency beta-Glucuronidase Deficiencies beta-Glucuronidase Deficiency |
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| Tree 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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D016538 | ||||||
| Scope note: | Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Mucopolysaccharidoses (1974-1991) |
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| Public MeSH Note: | 92 |
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| History Note: | 92 |
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| Entry Version: | MPS VII |
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| DeCS ID: | 29955 | ||||||
| Unique ID: | D016538 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1992/01/01 | ||||||
| Date of Entry: | 1991/06/21 | ||||||
| Revision Date: | 2013/07/08 |
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Mucopolysaccharidosis VII
- Preferred
| Concept UI |
M0025240 |
| Scope note | Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase. |
| Preferred term | Mucopolysaccharidosis VII |
| Entry term(s) |
Deficiencies, GUSB Deficiencies, beta-Glucuronidase Deficiency, GUSB Deficiency, beta-Glucuronidase Disease, Sly GUSB Deficiencies GUSB Deficiency Mucopolysaccharidosis 7 Mucopolysaccharidosis Type VII Mucopolysaccharidosis Type VIIs Mucopolysaccharidosis VIIs Sly Disease Sly Syndrome Syndrome, Sly Type VII, Mucopolysaccharidosis Type VIIs, Mucopolysaccharidosis VIIs, Mucopolysaccharidosis beta Glucuronidase Deficiency beta-Glucuronidase Deficiencies beta-Glucuronidase Deficiency |
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