| Descriptor English: | Mucopolysaccharidoses | ||||
| Descriptor Spanish: |
Mucopolisacaridosis
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| Descriptor Portuguese: | Mucopolissacaridoses | ||||
| Descriptor French: | Mucopolysaccharidoses | ||||
| Entry term(s): |
Mucopolysaccharidosis |
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| Tree number(s): |
C16.320.565.202.715 C16.320.565.595.600 C17.300.550.575 C18.452.648.202.715 C18.452.648.595.600 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D009083 | ||||
| Scope note: | Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. |
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| Annotation: | lysosomal storage dis; types I through VII except V are available as main headings: V = MUCOPOLYSACCHARIDOSIS V see MUCOPOLYSACCHARIDOSIS I; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
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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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| Public MeSH Note: | 92; was MUCOPOLYSACCHARIDOSIS 1974-91 |
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| Online Note: | use MUCOPOLYSACCHARIDOSES to search MUCOPOLYSACCHARIDOSIS 1974-91 |
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| History Note: | 92; was MUCOPOLYSACCHARIDOSIS 1974-91 |
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| DeCS ID: | 30388 | ||||
| Unique ID: | D009083 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 1974/01/01 | ||||
| Date of Entry: | 1999/01/01 | ||||
| Revision Date: | 2006/07/05 |
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Mucopolysaccharidoses
- Preferred
| Concept UI |
M0014167 |
| Scope note | Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. |
| Preferred term | Mucopolysaccharidoses |
| Entry term(s) |
Mucopolysaccharidosis |
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