GM2 gangliosidosis, HEXB-related, domestic cat

MONDO:1010884

A lysosomal storage disease in cats due to a mutation in the HEXB gene. There is a buildup of GM2 gangliosides in tissues due to the lack of the enzyme hexosaminidase. Characterised by progressive neuromuscular dysfunction and impaired growth from an early age.

Also known as: gangliosidosis, GM2, type II (Sandhoff or variant 0), domestic cat

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

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

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