Catalog

Restrictive cardiomyopathy due to storage disease

No MMS code

Link to WHO Definition

Restrictive cardiomyopathy due to storage disease – http://id.who.int/icd/entity/1721344709

Restrictive cardiomyopathy due to storage disease is the presence of restrictive cardiomyopathy in the presence of a glycogen, sphingolipidoses (such as α-galactosidase-A deficiency (Anderson-Fabry disease)), mucopolysaccharidoses (such as α-l iduronidase deficiency (Hurler syndrome)), iron-overload (such as haemochromatosis), or other storage disorder known to be significantly associated with restrictive cardiomyopathy.