GM2 gangliosidosis, HEXA-related, dog
MONDO:1012687A lysosomal storage disease that occurs in dogs due to a mutation in the HEXA gene.
Also known as: gangliosidosis, GM2, type I (B variant), dog
0 clinical trials for this condition and its sub-types.
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Disease
(618)
Gangliosidosis, dog
(0)
Gangliosidosis, non-human animal
(0)
Hereditary disease, non-human animal
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Inborn errors of metabolism, non-human animal
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Lysosomal storage disease, dog
(0)
Lysosomal storage disease, non-human animal
(0)
Metabolic disease, non-human animal
(0)
Non-human animal disease
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