Gaucher disease type 3 (Q84640): Difference between revisions
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13 August 2026
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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 |
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| 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). |
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CID11:ID_312650726
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dki-india-ID_312650726
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Concluído
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13 August 2026
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