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Glycogen storage disease, PYGM-related, cattle

MONDO:1010703

Any glycogen storage disease that occurs in cattle due to a mutation in the PYGM gene.

Also known as: myophosphorylase deficiency, cattle, glycogen storage disease V, cattle

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

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Broader categories

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

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