Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form
MONDO:0017699Also known as: GBE deficiency, childhood combined hepatic and myopathic form, GSD due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form, GSD type 4, childhood combined hepatic and myopathic form, GSDIV, childhood combined hepatic and myopathic form, glycogen storage disease type 4, childhood combined hepatic and myopathic form, glycogen storage disease type IV, childhood combined hepatic and myopathic form, glycogenosis due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form, glycogenosis type 4, childhood combined hepatic and myopathic form
1 clinical trial for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Disorder of glycogen metabolism
(14)
Human disease
(14)
Carbohydrate metabolism disease
(3)
Disease of genetic or genomic mechanism
(2)
Glycogen storage disease due to glycogen branching enzyme deficiency
(2)
Inborn carbohydrate metabolic disorder
(2)