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DeCS
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Descriptor English:
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Mannosidase Deficiency Diseases
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Descriptor Spanish:
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enfermedades por deficiencia de manosidasa
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Descriptor Portuguese:
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Doenças por Deficiência de Manosidase
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Synonyms English:
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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:
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C16.320.565.202.607
C16.320.565.595.577
C18.452.648.202.607
C18.452.648.595.577
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Definition English:
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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. |
See Related English:
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Mannosidases
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History Note English:
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2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003
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Allowable Qualifiers English:
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Record Number:
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38053
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Unique Identifier:
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D044904
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Occurrence in VHL:
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Similar:
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DeCS
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