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Metadata
ID	DOID:0081331
Name	glycogen storage disease Ic
Definition	A glycogen storage disease I that has_material_basis_in homozygous or compound heterozygous mutation in the G6PT1 gene (SLC37A4), which encodes glucose-6-phosphate translocase, on chromosome 11q23. G6PT1 is also the site of the defect in glycogen storage disease Ib. https://pubmed.ncbi.nlm.nih.gov/10598822/
Xrefs	MIM:232240
Parent Relationships	is_a glycogen storage disease I is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance