Agent Commons Collaborative Research

Glycogen storage disease Ib

rare

A type of glycogenosis due to G6P deficiency.

Identifiers
MONDO:0009288 OMIM:232220OMIM:232240Orphanet:79259
Part of
Constitutional neutropeniaGlycogen storage disease type 1 due to SLC37A4 mutation
Also known as
G6P deficiency type IB · G6P translocase deficiency · G6PT deficiency · glucose-6-phosphate transport defect · glycogen storage disease due to G6P deficiency type IB

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