U.S. National Library of Medicine
A group of recessively inherited diseases characterized by the intralysosomal accumulation of G(M2) GANGLIOSIDE in the neuronal cells. Subtypes include mutations of enzymes in the BETA-N-ACETYLHEXOSAMINIDASES system or G(M2) ACTIVATOR PROTEIN leading to disruption of normal degradation of GANGLIOSIDES, a subclass of ACIDIC GLYCOSPHINGOLIPIDS.
The numerical value of gangliosidoses, gm2 in Chaldean Numerology is: 2
The numerical value of gangliosidoses, gm2 in Pythagorean Numerology is: 4
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