GM2 gangliosidosis, rabbit

MONDO:1012691

A lysosomal storage disease that occurs in rabbits in which there is a buildup of GM2 gangliosides in the brain due to the lack of the enzyme β-hexosaminidase A. It is characterised by rapidly progression of neurological signs.

Also known as: gangliosidosis, GM2, type I (B variant), rabbit

0 clinical trials for this condition and its sub-types, 0 tagged with GM2 gangliosidosis, rabbit itself.

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↑ Gangliosidosis, non-human animal (0)

Including sub-types (0) Tagged with GM2 gangliosidosis, rabbit (0)

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