Catalog

Hypertrophic cardiomyopathy due to lysosomal storage disease

No MMS code

Link to WHO Definition

Hypertrophic cardiomyopathy due to lysosomal storage disease – http://id.who.int/icd/entity/1286416076

Hypertrophic cardiomyopathy due to a lysosomal storage disorder is the presence of hypertrophic cardiomyopathy in association with the lysosomal accumulation of any of a variety of accumulated substrates as seen in the sphingolipidoses (such as α-galactosidase-A deficiency (Anderson-Fabry disease)), oligosaccharidoses, mucolipidoses (such as I-cell disease), mucopolysaccharidoses (such as α-liduronidase deficiency (Hurler syndrome)), lipoprotein storage disorders, lysosomal transport defects, and others.