Glycogen storage disease IX
MONDO:0700291A group of inborn errors of glycogen metabolism that is clinically and genetically heterogeneous. This group comprises GSD due to liver phosphorylase kinase (PhK) deficiency, GSD due to muscle PhK deficiency and GSD due to liver and muscle PhK deficiency.
Also known as: GSD IX, GSD type 9, GSD type IX, GSD9, GSDIX, glycogen storage disease 9, glycogen storage disease IX, glycogen storage disease type 9
3 clinical trials for this condition and its sub-types.
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Broader categories
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)
Inborn carbohydrate metabolic disorder
(2)
Inborn disorder of energy metabolism
(1)