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Concept information

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

Terme préférentiel

Mannosidase Deficiency Diseases  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Concepts spécifiques

Concepts associés

Synonyme(s)

  • Mannosidase Deficiency Syndromes
  • Mannosidosis

Qualificatif(s) autorisé(s)

Traductions

  • Mannosidoses

    français

  • 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 Date de création 09/07/2003, dernière modification le 08/07/2013