Mucopolysaccharidosis type 6 (Q40079): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A mucopolissacaridose tipo VI (tipo 6) é uma doença de depósito lisossomal com envolvimento multissistêmico progressivo, associada à deficiência de arilsulfatase B levando ao acúmulo de sulfato de dermatan. O transtorno mostra um amplo espectro de sintomas, desde formas de progressão lenta a rápida.
@@ description / en / description / en @@
+Mucopolysaccharidosis type 6 (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate. The disorder shows a wide spectrum of symptoms from slowly to rapidly progressing forms.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1288379621
@@ Property / Canonical URI: https://id.who.int/icd/entity/1288379621 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:5C56.33
@@ Property / CURIE: CID11:5C56.33 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-5C56.33
@@ Property / Canary Token: dki-india-5C56.33 / 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
@@ Property / Linked ICD 10 @@
+E76.2
@@ Property / Linked ICD 10: E76.2 / rank @@
+Normal rank

Latest revision as of 05:44, 13 August 2026

Mucopolysaccharidosis type 6 (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate. The disorder shows a wide spectrum of symptoms from slowly to rapidly progressing forms.

Language	Label	Description	Also known as
default for all languages	5C56.33
English	Mucopolysaccharidosis type 6	Mucopolysaccharidosis type 6 (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate. The disorder shows a wide spectrum of symptoms from slowly to rapidly progressing forms.