Nonclassical phenylketonuria (Q39988): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A fenilcetonúria leve é uma forma rara de fenilcetouria (PKU), um erro inato do metabolismo de aminoácidos, caracterizado por sintomas de PKU de gravidade leve a moderada.
@@ description / en / description / en @@
+Mild phenylketonuria is a rare form of phenylketonuria (PKU), an inborn error of amino acid metabolism, characterised by symptoms of PKU of mild to moderate severity.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/2132400826
@@ Property / Canonical URI: https://id.who.int/icd/entity/2132400826 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:5C50.01
@@ Property / CURIE: CID11:5C50.01 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-5C50.01
@@ Property / Canary Token: dki-india-5C50.01 / 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 @@
+E70.1
@@ Property / Linked ICD 10: E70.1 / rank @@
+Normal rank

Latest revision as of 05:37, 13 August 2026

Mild phenylketonuria is a rare form of phenylketonuria (PKU), an inborn error of amino acid metabolism, characterised by symptoms of PKU of mild to moderate severity.

Language	Label	Description	Also known as
default for all languages	5C50.01
English	Nonclassical phenylketonuria	Mild phenylketonuria is a rare form of phenylketonuria (PKU), an inborn error of amino acid metabolism, characterised by symptoms of PKU of mild to moderate severity.