GM1 gangliosidosis (Q90733): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A gangliosidose GM1 é uma doença rara de depósito lisossomal caracterizada bioquimicamente pela atividade deficiente da beta-galactosidase e clinicamente por uma ampla gama de características neuroviscerais, oftalmológicas e dismórficas.
@@ description / en / description / en @@
+GM1 gangliosidosis is a rare lysosomal storage disorder characterised biochemically by deficient beta-galactosidase activity and clinically by a wide range of variable neurovisceral, ophthalmological and dysmorphic features.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/401105928
@@ Property / Canonical URI: https://id.who.int/icd/entity/401105928 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_401105928
@@ Property / CURIE: CID11:ID_401105928 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_401105928
@@ Property / Canary Token: dki-india-ID_401105928 / 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 17:43, 15 August 2026

GM1 gangliosidosis is a rare lysosomal storage disorder characterised biochemically by deficient beta-galactosidase activity and clinically by a wide range of variable neurovisceral, ophthalmological and dysmorphic features.

Language	Label	Description	Also known as
default for all languages	ID_401105928
English	GM1 gangliosidosis	GM1 gangliosidosis is a rare lysosomal storage disorder characterised biochemically by deficient beta-galactosidase activity and clinically by a wide range of variable neurovisceral, ophthalmological and dysmorphic features.