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The way concept relations are shown:
G(M2) Ganglioside
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ G(M2) Ganglioside 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ G(M2) Ganglioside 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ G(M2) Ganglioside 2 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ G(M2) Ganglioside 2 coordinate conceptsX |
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History note: | Gangliosides (1974)X |
historyNote*: | 91(75); was see under GANGLIOSIDES 1975-90
X |
publicMeSHNote*: | 91; was see under GANGLIOSIDES 1975-90
X |
Scope note: | A glycosphingolipid that accumulates due to a deficiency of hexosaminidase A or B (BETA-N-ACETYLHEXOSAMINIDASE), or GM2 activator protein, resulting in GANGLIOSIDOSES, heredity metabolic disorders that include TAY-SACHS DISEASE and SANDHOFF DISEASE.
X |
activeMeSHYear*: | |
dateCreated*: | 1974-11-19X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2004-07-07X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | ssbX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | G(M2)-gangliosidi (fi) XTay-Sachs Disease Ganglioside (en, replaced) Ganglioside GM2 (en, replaced) Gangliósido G(M2) (es) γαγγλιοσίδιο G(M2) (el) G(M2)-Gangliosid (de) G(M2) gangliosid (cs) Gangliosido de la Enfermedad de Tay-Sach (es, replaced) Tay-Sachs-Gangliosid (de, replaced) |
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