Glycogen storage disease due to muscle glycogen phosphorylase kinase deficiency (Q100848): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A doença de depósito de glicogênio devido à deficiência de fosforilase quinase muscular é um erro inato benigno do metabolismo do glicogênio caracterizado pela intolerância ao exercício.
@@ description / en / description / en @@
+Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterised by exercise intolerance.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/273845529
@@ Property / Canonical URI: https://id.who.int/icd/entity/273845529 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_273845529
@@ Property / CURIE: CID11:ID_273845529 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_273845529
@@ Property / Canary Token: dki-india-ID_273845529 / 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 +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 17:37, 16 August 2026

Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterised by exercise intolerance.

Language	Label	Description	Also known as
default for all languages	ID_273845529
English	Glycogen storage disease due to muscle glycogen phosphorylase kinase deficiency	Glycogen storage disease due to muscle phosphorylase kinase (PhK) deficiency is a benign inborn error of glycogen metabolism characterised by exercise intolerance.