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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

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Mannosidase Deficiency Diseases  

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Tipo

  • mesh:Descriptor

Definición

  • 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.

Concepto genérico

Conceptos específicos

Conceptos relacionados

Etiquetas alternativas

  • Mannosidase Deficiency Syndromes
  • Mannosidosis

En otras lenguas

  • Mannosidoses

    francés

  • 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 Creado 9/7/03, última modificación 8/7/13