| Descriptor English: | Mannosidase Deficiency Diseases | ||||||
| Descriptor Spanish: |
Enfermedades por Deficiencia de Manosidasa
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| Descriptor Portuguese: | Doenças por Deficiência de Manosidase | ||||||
| Descriptor French: | Mannosidoses | ||||||
| Entry term(s): |
Deficiency Disease, Mannosidase Deficiency Diseases, Mannosidase Deficiency Syndrome, Mannosidase Deficiency Syndromes, Mannosidase Diseases, Mannosidase Deficiency Mannosidase Deficiency Disease Mannosidase Deficiency Syndrome Mannosidase Deficiency Syndromes Mannosidoses Mannosidosis |
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| Tree number(s): |
C16.320.565.202.607 C16.320.565.595.577 C18.452.648.202.607 C18.452.648.595.577 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D044904 | ||||||
| Scope note: | Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme. |
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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: |
Mannosidosis (1984-2003) |
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| Public MeSH Note: | 2004; see MANNOSIDOSIS 1984-2003 |
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| History Note: | 2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003 |
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| Entry Version: | MANNOSIDASE DEFIC DIS |
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| Related: |
Mannosidases
MeSH | ||||||
| DeCS ID: | 38053 | ||||||
| Unique ID: | D044904 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2004/01/01 | ||||||
| Date of Entry: | 2003/07/09 | ||||||
| Revision Date: | 2013/07/08 |
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Mannosidase Deficiency Diseases
- Preferred
| Concept UI |
M0446510 |
| Scope note | Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme. |
| Preferred term | Mannosidase Deficiency Diseases |
| Entry term(s) |
Deficiency Disease, Mannosidase Deficiency Diseases, Mannosidase Deficiency Syndrome, Mannosidase Deficiency Syndromes, Mannosidase Diseases, Mannosidase Deficiency Mannosidase Deficiency Disease Mannosidase Deficiency Syndrome Mannosidase Deficiency Syndromes Mannosidoses Mannosidosis |
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