Encephalopathy due to prosaposin deficiency (Q55455): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A encefalopatia por deficiência de prosaposina é uma doença de depósito lisossomal pertencente ao grupo das esfingolipidoses e é uma doença neurovisceral grave que se manifesta imediatamente após o nascimento e segue um curso fatal de progressão muito rápida.
@@ description / en / description / en @@
+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.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/935370911
@@ Property / Canonical URI: https://id.who.int/icd/entity/935370911 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_935370911
@@ Property / CURIE: CID11:ID_935370911 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_935370911
@@ Property / Canary Token: dki-india-ID_935370911 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest 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.