Disorder of glycogen metabolism
MONDO:0002412An inherited metabolic disorder characterized either by defects in glycogen synthesis or defects in the breaking down of glycogen. It results either in the creation of abnormal forms of glycogen or accumulation of glycogen in the tissues.
Also known as: GSD, glycogen storage disease, glycogen storage disorder, glycogenoses, glycogenosis, inborn error of glycogen metabolic process, inborn glycogen metabolic process disorder, inborn glycogen storage disorder
87 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Glycogen storage disease II
(28)
Glycogen storage disease due to acid maltase deficiency, late-onset
(16)
Glycogen storage disease due to acid maltase deficiency, infantile onset
(9)
Glycogen storage disease I
(8)
Glycogen storage disease due to glucose-6-phosphatase deficiency type IA
(7)
Danon disease
(5)
Glycogen storage disease Ib
(3)
Glycogen storage disease IXa1
(2)
Glycogen storage disease IXa2
(2)
Glycogen storage disease IXb
(2)
Glycogen storage disease IXc
(2)
Glycogen storage disease V
(2)
Adult polyglucosan body disease
(1)
Glycogen storage disease due to GLUT2 deficiency
(1)
Glycogen storage disease due to glycogen branching enzyme deficiency
(1)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency
(1)
Glycogen storage disease due to muscle beta-enolase deficiency
(1)
Glycogen storage disease due to phosphoglycerate mutase deficiency
(1)
Glycogen storage disease III
(1)
Glycogen storage disease IX
(1)
Broader categories
Disease
(618)
Metabolic disease
(215)
Hereditary disease
(172)
Inborn errors of metabolism
(42)
Human disease
(14)
Carbohydrate metabolism disease
(3)
Disease of genetic or genomic mechanism
(2)
Inborn carbohydrate metabolic disorder
(2)
Inborn disorder of energy metabolism
(1)
Disease by developmental or physiological process
(0)