Sjukdomar orsakade av förlust av ett eller fler enzym som deltar i hydrolys av mannosidlänkningar (mannosidaser). Bristerna i enzymaktivitet är främst förknippade med mutation av de gener som kodar för ett särskilt mannosidasisoenzym.
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.
Mannosidos
Deficiency Disease, Mannosidase — Deficiency Diseases, Mannosidase — Diseases, Mannosidase Deficiency — Mannosidase Deficiency Disease — Mannosidase Deficiency Syndromes — Deficiency Syndrome, Mannosidase — Deficiency Syndromes, Mannosidase — Mannosidase Deficiency Syndrome — Mannosidosis — Mannosidoses