Danon disease
MONDO:0010281A lysosomal glycogen storage disease characterized by severe cardiomyopathy and variable degrees of muscle weakness, frequently associated with intellectual deficit.
Also known as: ANTOPOL disease, Danon disease, Danon disease, X-linked dominant, GSD due to LAMP-2 deficiency, LAMP2 lysosomal glycogen storage disease, glycogen storage disease type IIb, glycogenosis due to LAMP-2 deficiency, lysosomal glycogen storage disease caused by mutation in LAMP2
6 clinical trials for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Lysosomal storage disease
(35)
Disorder of glycogen metabolism
(14)
Human disease
(14)
Carbohydrate metabolism disease
(3)
Disease of genetic or genomic mechanism
(2)
Inborn carbohydrate metabolic disorder
(2)