GM2 gangliosidosis, GM2A-related, domestic cat

MONDO:1010878

A lysosomal storage disease in cats due to a mutation in the GM2A gene. There is a buildup of G(M2) gangliosides in tissues. It is characterised by progressive neuromuscular dysfunction.

Also known as: gangliosidosis, GM2, GM2A, (AB variant) domestic cat

0 clinical trials for this condition and its sub-types, 0 tagged with GM2 gangliosidosis, GM2A-related, domestic cat itself.

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Including sub-types (0) Tagged with GM2 gangliosidosis, GM2A-related, domestic cat (0)

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