MeSH Browser

MeSH Heading: Mannosidase Deficiency Diseases
Tree Number(s): C16.320.565.202.607; C16.320.565.595.577; C18.452.648.202.607; C18.452.648.595.577
Unique ID: D044904
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D044904
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.
Entry Version: MANNOSIDASE DEFIC DIS
Entry Term(s): Mannosidase Deficiency Syndromes; Mannosidosis
Previous Indexing: Mannosidosis (1984-2003)
See Also: Mannosidases
Public MeSH Note: 2004; see MANNOSIDOSIS 1984-2003
History Note: 2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003
Date Established: 2004/01/01
Date of Entry: 2003/07/09
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Mannosidase Deficiency Diseases MeSH Descriptor Data 2025