Glycogen storage disease Ib

MONDO:0009288

A type of glycogenosis due to G6P deficiency.

Also known as: G6P deficiency type IB, G6P translocase deficiency, G6PT deficiency, GSD Ib, GSD due to G6P deficiency type IB, GSD due to G6PT deficiency, GSD type 1 non a, GSD type 1b

4 clinical trials for this condition and its sub-types, 3 tagged with Glycogen storage disease Ib itself.

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Where it sits in the disease tree

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Part of

↑ Constitutional neutropenia (28) ↑ Glycogen storage disease type 1 due to SLC37A4 mutation (3)

Including sub-types (4) Tagged with Glycogen storage disease Ib (3)

Trials to join now! 1 Not yet finished but already full! 2

Can home tests replace lab draws for rare disease patients?

Diagnosis Recruiting now

This study aims to see if a home lactate meter and a standard glucose meter give accurate readings compared to lab tests in people with glycogen storage disease types Ia, Ib, and XI. Ten participants will have an 8-hour hospital stay with hourly blood draws and finger-stick tests…

Sponsor: Connecticut Children's Medical Center • Aim: Diagnosis

Last updated Jun 27, 2026 13:01 UTC

Glycogen storage disease Ib

Where it sits in the disease tree

Can home tests replace lab draws for rare disease patients?