Encephalopathy due to prosaposin deficiency (Q55455): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
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
0 references
dki-india-ID_935370911
0 references
Concluído
0 references
