Catalog

Dilated cardiomyopathy due to lysosomal storage disorder

No MMS code

Link to WHO Definition

Dilated cardiomyopathy due to lysosomal storage disorder – http://id.who.int/icd/entity/418533851

Dilated cardiomyopathy due to a lysosomal storage disorder is the presence of dilated cardiomyopathy in association with the lysosomal accumulation of any of a variety of accumulated substrates as seen in the sphingolipidoses (such as Gaucher disease), oligosaccharidoses, mucolipidoses, mucopolysaccharidoses, lipoprotein storage disorders, lysosomal transport defects, neuronal ceroid lipofuscinoses, and others.