Catalog

Gaucher disease type 3

No MMS code

Link to WHO Definition

Gaucher disease type 3 – http://id.who.int/icd/entity/312650726

Gaucher disease type 3 is the subacute neurological form of Gaucher disease (a lysosomal storage disorder caused by a deficiency in glucocerebrosidase) characterised by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1 (see this term).