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What (who) is GM2 gangliosidoses - definition
GM2 gangliosidoses
HUMAN DISEASE
GM2 gangliosidosis; Gangliosidoses gm2; Gangliosidosis gm1; GM2 Gangliosidosis; Gangliosidosis (Type2)(GM2); Gm2 gangliosidoses; Gangliosidoses GM2; Gangliosidosis GM1
The GM2 gangliosidoses are a group of three related genetic disorders that result from a deficiency of the enzyme beta-hexosaminidase. This enzyme catalyzes the biodegradation of fatty acid derivatives known as gangliosides.
GM2A
MAMMALIAN PROTEIN FOUND IN HOMO SAPIENS
Ganglioside GM2 activator protein; GM2 ganglioside activator; GM2A (gene)
GM2 ganglioside activator also known as GM2A is a protein which in humans is encoded by the GM2A gene.
Gangliosidosis
HUMAN DISEASE
Gangliosidoses
Gangliosidosis contains different types of lipid storage disorders caused by the accumulation of lipids known as gangliosides. There are two distinct genetic causes of the disease.
