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GM2 gangliosidosis, HEXA-related, sheep

MONDO:1012690

A lysosomal storage disease that occurs in sheep due to a mutation in the HEXA gene.

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

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Gangliosidosis, non-human animal (0) Hereditary disease, non-human animal (0) Inborn errors of metabolism, non-human animal (0) Lysosomal storage disease, non-human animal (0) Metabolic disease, non-human animal (0) Non-human animal disease (0)

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