Mannosidase Deficiency Diseases [nemoci z nedostatku mannosidázy]
topical
1
- Terms
-
mannosidasy - nemoci z nedostatku
mannosidóza
-
Mannosidase Deficiency Syndromes
Mannosidosis
Persistent link
https://www.medvik.cz/link/D044904
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.
- DUI
- D044904 MeSH Browser
- CUI
- M0446510
- Previous indexing
- Mannosidosis (1984-2003)
- History note
- 2004; use MANNOSIDOSIS, ALPHA B, LYSOSOMAL 1984-2003
- Public note
- 2004; see MANNOSIDOSIS 1984-2003
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology 1
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics 1
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology 1
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology
...
Occurrences in Medvik records
C
Diseases
C16.320.565.202.720
Multiple Carboxylase Deficiency
C16.320.565.595.100
Aspartylglucosaminuria
C18.452.648.202.720
Multiple Carboxylase Deficiency
C18.452.648.595.100
Aspartylglucosaminuria