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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Mannosidase Deficiency Diseases
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Mannosidase Deficiency Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lysosomal Storage Diseases > Mannosidase Deficiency Diseases
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lysosomal Storage Diseases > Mannosidase Deficiency Diseases

Preferred term

Mannosidase Deficiency Diseases  

Type

  • mesh:Descriptor

Definition

  • 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.

Broader concept

Narrower concepts

Related concepts

Entry terms

  • Mannosidase Deficiency Syndromes
  • Mannosidosis

Allowable Qualifier(s)

In other languages

  • Mannosidoses

    French

  • Déficits en mannosidase
  • Maladies dues au déficit en mannosidase

URI

http://data.loterre.fr/ark:/67375/JVR-B2CPSJS3-Z

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RDF/XML TURTLE JSON-LD Created 7/9/03, last modified 7/8/13