Mucopolysaccharidoses [mukopolysacharidózy]
topical
81
- Terms
-
mukopolysacharidosa
mukopolysacharidosy
mukopolysacharidóza
-
Mucopolysaccharidosis
Persistent link
https://www.medvik.cz/link/D009083
Definition
Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
- Annotation
- lysosomal storage dis; types I through VII except V are available as main headings: V = MUCOPOLYSACCHARIDOSIS V see MUCOPOLYSACCHARIDOSIS I; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
- DUI
- D009083 MeSH Browser
- CUI
- M0014167
- History note
- 92; was MUCOPOLYSACCHARIDOSIS 1974-91
- Online note
- use MUCOPOLYSACCHARIDOSES to search MUCOPOLYSACCHARIDOSIS 1974-91
- Public note
- 92; was MUCOPOLYSACCHARIDOSIS 1974-91
Allowable subheadings
- BL
- blood 0
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 10
- CO
- complications 7
- DI
- diagnosis 32
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 5
- EC
- economics 1
- EM
- embryology 0
- EN
- enzymology 1
- EP
- epidemiology 1
- EH
- ethnology 0
- ET
- etiology 5
- GE
- genetics 8
- HI
- history 0
- IM
- immunology 0
- ME
- metabolism 6
- MI
- microbiology 0
- MO
- mortality 1
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 6
- PP
- physiopathology 9
- PC
- prevention & control 1
- PX
- psychology 3
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 0
- TH
- therapy 27
- UR
- urine 1
- VE
- veterinary 0
- VI
- virology 0
...
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