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G(M2) gangliozid

  1. Record numberd005678
    Date06.06.2025
    TypeM - MESH
    Topical termG(M2) gangliozid
    Other termEnglish (Pseudonym) GM2 Ganglioside
    English (Pseudonym) Tay-Sachs Disease Ganglioside
    Slovak (Pseudonym) GM2 gangliozid
    Slovak (Pseudonym) gangliozid Tayovej-Sachsovej choroby
    Slovak (Pseudonym) gangliozid Tay-Sachsovej choroby
    See also(Skutočné meno) Sandhoffova choroba
    (Skutočné meno) Tay-Sachsova choroba
    UDCD09.400.410.420.025.475.400D10.390.470.025.475.400D10.570.877.360.025.475.400
    NoteA 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.
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Number of the records: 1  

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