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, 0 tagged with GM2 gangliosidosis, HEXA-related, sheep itself.

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