Carnosinaemia (Q39999): Difference between revisions

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@@ Property / CURIE @@
+CID11:5C50.F1
@@ Property / CURIE: CID11:5C50.F1 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-5C50.F1
@@ Property / Canary Token: dki-india-5C50.F1 / 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 @@
+E70.8
@@ Property / Linked ICD 10: E70.8 / rank @@
+Normal rank

Latest revision as of 05:38, 13 August 2026

Carnosinaemia is a very rare inherited disorder of the metabolism of peptides that presents with serum carnosinase deficiency, variable degrees of intellectual deficit, sometimes with seizures, while a few patients are asymptomatic.

Language	Label	Description	Also known as
default for all languages	5C50.F1
English	Carnosinaemia	Carnosinaemia is a very rare inherited disorder of the metabolism of peptides that presents with serum carnosinase deficiency, variable degrees of intellectual deficit, sometimes with seizures, while a few patients are asymptomatic.