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

Preferred term

Mannosidase Deficiency Diseases  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Related concepts

Entry terms

  • Deficiency Syndrome, Mannosidase
  • Deficiency Syndromes, Mannosidase
  • Mannosidase Deficiency Syndrome
  • Mannosidase Deficiency Syndromes
  • Mannosidoses
  • Mannosidosis

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.

History note

  • 2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003

In other languages

  • mannosidoosit

    Finnish

  • mannosidaasipuute
  • mannosidaasipuutesairaudet
  • mannosidaasipuutesairaus
  • mannosidaasipuutos
  • mannosidaasipuutossairaudet
  • mannosidaasipuutossairaus
  • mannosidoosi
  • Mannosidasbristsjukdomar

    Swedish

  • Mannosidos

URI

http://www.yso.fi/onto/mesh/D044904

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