Glycogen storage disease due to liver phosphorylase kinase deficiency
MONDO:0020693A benign form of phosphorylase kinase deficiency caused by variants in PHKA2 or PHKG2 and characterized by hepatomegaly, growth retardation, and mild delay in motor development during childhood.
3 clinical trials for this condition and its sub-types, 0 tagged with Glycogen storage disease due to liver phosphorylase kinase deficiency itself.
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Browse by category →Sub-types of Glycogen storage disease due to liver phosphorylase kinase deficiency
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Glycogen storage disease IXa1 2 trials
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Glycogen storage disease IXc 2 trials
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