Glycogen storage disease Ib
MONDO:0009288A 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.
Follow this condition — get notified about new trialsBroader categories
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Can home tests replace lab draws for rare disease patients?
Diagnosis Recruiting nowThis 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
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Can a national registry unlock the genetic secrets of glycogen storage diseases in indian children?
Knowledge-focused Recruiting nowThis study aims to create a nationwide registry of Indian children with hepatic glycogen storage diseases (GSDs), a group of inherited metabolic disorders affecting the liver and muscles. By collecting genetic, clinical, and outcome data from 250 children, researchers hope to map…
Sponsor: Institute of Liver and Biliary Sciences, India • Aim: Knowledge-focused
Last updated Aug 07, 2026 00:00 UTC