Classical phenylketonuria (Q39986): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A fenilcetonúria clássica é uma forma grave de fenilcetonúria (PKU), um erro inato do metabolismo dos aminoácidos, caracterizado por déficit intelectual grave e complicações neuropsiquiátricas em pacientes não tratados.
@@ description / en / description / en @@
+Classical phenylketonuria is a severe form of phenylketonuria (PKU) an inborn error of amino acid metabolism characterised in untreated patients by severe intellectual deficit and neuropsychiatric complications.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/2084504393
@@ Property / Canonical URI: https://id.who.int/icd/entity/2084504393 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:5C50.00
@@ Property / CURIE: CID11:5C50.00 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-5C50.00
@@ Property / Canary Token: dki-india-5C50.00 / 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 @@
+E70.0
@@ Property / Linked ICD 10: E70.0 / rank @@
+Normal rank

Latest revision as of 05:37, 13 August 2026

Classical phenylketonuria is a severe form of phenylketonuria (PKU) an inborn error of amino acid metabolism characterised in untreated patients by severe intellectual deficit and neuropsychiatric complications.

Language	Label	Description	Also known as
default for all languages	5C50.00
English	Classical phenylketonuria	Classical phenylketonuria is a severe form of phenylketonuria (PKU) an inborn error of amino acid metabolism characterised in untreated patients by severe intellectual deficit and neuropsychiatric complications.