Gaucher disease type 3 (Q84640): Difference between revisions

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Latest revision as of 09:59, 15 August 2026

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).

Language	Label	Description	Also known as
default for all languages	ID_312650726
English	Gaucher disease type 3	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).