Cure My Disease

Don't miss your cure!

 Log in / Sign up

Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form

MONDO:0017698

Also known as: GBE deficiency, congenital neuromuscular form, GSD due to glycogen branching enzyme deficiency, congenital neuromuscular form, GSD type 4, congenital neuromuscular form, GSDIV, congenital neuromuscular form, glycogen storage disease type 4, congenital neuromuscular form, glycogen storage disease type IV, congenital neuromuscular form, glycogenosis due to glycogen branching enzyme deficiency, congenital neuromuscular form, glycogenosis type 4, congenital neuromuscular form

24 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (618) Metabolic disease (215) Hereditary disease (172) Inborn errors of metabolism (42) Human disease (14) Disorder of glycogen metabolism (11) Carbohydrate metabolism disease (3) Disease of genetic or genomic mechanism (2) Inborn carbohydrate metabolic disorder (2) Glycogen storage disease due to glycogen branching enzyme deficiency (1)
Trials to join now! 13 Not yet recruiting 3 Not yet finished but already full! 3 Completed 5
Sort by