Encephalopathy due to prosaposin deficiency (Q55455): Difference between revisions
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Revision as of 03:06, 14 August 2026
Encephalopathy due to prosaposin deficiency is a lysosomal storage disease belonging to the group of sphingolipidoses, and is a severe neurovisceral disease manifesting immediately after birth and following a rapidly progressive fatal course.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_935370911 |
||
| English | Encephalopathy due to prosaposin deficiency |
Encephalopathy due to prosaposin deficiency is a lysosomal storage disease belonging to the group of sphingolipidoses, and is a severe neurovisceral disease manifesting immediately after birth and following a rapidly progressive fatal course. |
Statements
CID11:ID_935370911
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