Glycogen storage disease XV
MONDO:0013291Glycogen storage disease type 15 is an extremely rare genetic glycogen storage disease reported in one patient to date. Clinical signs included muscle weakness, cardiac arrhythmia associated with accumulation of abnormal storage material in the heart and glycogen depletion in skeletal muscle.
Also known as: GSD type 15, GSD type XV, GSD with severe cardiomyopathy due to glycogenin deficiency, glycogen storage disease XV, glycogen storage disease type 15, glycogen storage disease type XV, glycogenosis type 15, glycogenosis type XV
1 clinical trial for this condition and its sub-types.
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Disease
(717)
Metabolic disease
(241)
Hereditary disease
(188)
Inborn errors of metabolism
(47)
Disorder of glycogen metabolism
(15)
Human disease
(15)
Carbohydrate metabolism disease
(4)
Disease of genetic or genomic mechanism
(2)
Inborn carbohydrate metabolic disorder
(2)
Inborn disorder of energy metabolism
(1)