GM1 gangliosidosis

MONDO:0018149

A rare lysosomal storage disorder characterized biochemically by deficient beta-galactosidase activity and clinically by a wide range of variable neurovisceral, ophthalmological and dysmorphic features.

Also known as: Beta-galactosidase-1 deficiency, GLB1 deficiency, GM>1< gangliosidosis, Landing disease, Landing syndrome, gangliosidosis GM1, Beta galactosidase 1 deficiency, Beta-galactosidosis

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