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.
ID
http://purl.bioontology.org/ontology/MESH/D044904
altLabel
Mannosidase Deficiency Disease
Diseases, Mannosidase Deficiency
Mannosidase Deficiency Syndrome
Deficiency Disease, Mannosidase
Mannosidase Deficiency Syndromes
Mannosidosis
Deficiency Syndromes, Mannosidase
Deficiency Syndrome, Mannosidase
Mannosidoses
Deficiency Diseases, Mannosidase
AQL
BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
cui
C1257960
DC
1
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.
DX
20040101
FX
D008361
HN
2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003