- Concept UI
- M0008925
- Scope Note
- A glycosphingolipid that accumulates due to a deficiency of hexosaminidase A or B (BETA-N-ACETYLHEXOSAMINIDASES), or GM2 activator protein, resulting in GANGLIOSIDOSES, heredity metabolic disorders that include TAY-SACHS DISEASE and SANDHOFF DISEASE.
- Terms
-
G(M2) Ganglioside
Preferred Term
Term UI
T017174
Date01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1975)
-
GM2 Ganglioside
Term UI
T000952288
Date02/28/2019
LexicalTag
NON
ThesaurusID
NLM (2020)
-
Tay-Sachs Disease Ganglioside
Term UI
T017175
Date05/20/1976
LexicalTag
EPO
ThesaurusID
UNK (19XX)
-
Ganglioside GM2
Term UI
T017176
Date04/23/1988
LexicalTag
NON
ThesaurusID
UNK (19XX)