GM2 gangliosidosis, HEXB-related, domestic cat
MONDO:1010884A 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.
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Disease
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Gangliosidosis, domestic cat
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Gangliosidosis, non-human animal
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Hereditary disease, non-human animal
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Inborn errors of metabolism, non-human animal
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Lysosomal storage disease, domestic cat
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Lysosomal storage disease, non-human animal
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Metabolic disease, non-human animal
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Non-human animal disease
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