Mannosidase Deficiency Diseases

**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.

**Tree numbers:** - C16.320.565.202.607 - C16.320.565.595.577 - C18.452.648.202.607 - C18.452.648.595.577

**Synonyms:** - Mannosidosis - Mannosidase Deficiency Syndromes