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Mannosidase Deficiency Diseases
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.
Subtype terms (2)
More specific conditions that are subtypes of Mannosidase Deficiency Diseases in the MeSH hierarchy.
- alpha-Mannosidosis
12 drugs (9 approved, 3 experimental)
- beta-Mannosidosis
Drugs by status
Organizations
Organization Involved with Phase 3 Indications (5)
Organization Involved with Phase 2 Indications (5)
Organization Involved with Phase 1 Indications (1)