Gangliosidoses [gangliosidóza]
topical
11
- Terms
-
Ganglioside Storage Diseases
Ganglioside Storage Disorders
Gangliosidosis
Persistent link
https://www.medvik.cz/link/D005733
Definition
A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway.
- Annotation
- coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and GANGLIOSIDOSES, GM2 are available
- kombinuj IM s konkrétním gangliosidem (IM), ale k dispozici jsou i deskriptory GANGLIOSIDÓZA GM1 a GANGLIOSIDÓZY GM2
- DUI
- D005733 MeSH Browser
- CUI
- M0008988
- Previous indexing
- Lipoidosis (1966-1975); Gangliosides (1966-1975)
- History note
- 1992(1976)
- Public note
- 1992; see GANGLIOSIDOSIS 1976-91
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis 4
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 1
- EH
- ethnology 1
- ET
- etiology 5
- GE
- genetics 1
- HI
- history
- IM
- immunology
- ME
- metabolism 1
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 2
- PP
- physiopathology
- 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