Familial pseudohyperkalaemia (Q39535): Difference between revisions

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@@ Property / CURIE @@
+CID11:3A10.3
@@ Property / CURIE: CID11:3A10.3 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-3A10.3
@@ Property / Canary Token: dki-india-3A10.3 / 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
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
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+day
 Before
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@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ Property / Linked ICD 10 @@
+D58.8
@@ Property / Linked ICD 10: D58.8 / rank @@
+Normal rank

Latest revision as of 04:59, 13 August 2026

A disease caused by a genetically inherited mutation. This disease is characterised by a temperature-dependent defect in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C leading to elevated potassium levels in the blood that does not reflect the true potassium level. Confirmation is by identification of genetic mutation through genetic testing.

Language	Label	Description	Also known as
default for all languages	3A10.3
English	Familial pseudohyperkalaemia	A disease caused by a genetically inherited mutation. This disease is characterised by a temperature-dependent defect in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C leading to elevated potassium levels in the blood that does not reflect the true potassium level. Confirmation is by identification of genetic mutation through genetic testing.