An X-linked dominant multisystem disorder resulting in cardiomyopathy, myopathy and INTELLECTUAL DISABILITY. It is caused by mutation in the gene encoding LYSOSOMAL-ASSOCIATED MEMBRANE PROTEIN 2.
Also Known As:
Antopol Disease; Danon Disease; Glycogen Storage Cardiomyopathy; Glycogen Storage Disease IIb; Glycogen Storage Disease Limited to the Heart; Glycogen Storage Disease Type 2B; Lysosomal Glycogen Storage Disease with Normal Acid Maltase; Lysosomal Glycogen Storage Disease without Acid Maltase Deficiency; Pseudoglycogenosis 2; Pseudoglycogenosis II; Vacuolar Cardiomyopathy and Myopathy, X-linked; X-Linked Vacuolar Cardiomyopathy and Myopathy; Cardiomyopathies, Glycogen Storage; Cardiomyopathy, Glycogen Storage; Disease, Antopol; Glycogen Storage Cardiomyopathies; Pseudoglycogenosis 2s; Pseudoglycogenosis IIs; Vacuolar Cardiomyopathy and Myopathy, X linked; X Linked Vacuolar Cardiomyopathy and Myopathy