Porokeratoses (Q44109): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/29524620
@@ Property / Canonical URI: https://id.who.int/icd/entity/29524620 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ED52
@@ Property / CURIE: CID11:ED52 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ED52
@@ Property / Canary Token: dki-india-ED52 / 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 @@
+L85.9
@@ Property / Linked ICD 10: L85.9 / rank @@
+Normal rank

Latest revision as of 11:26, 13 August 2026

Porokeratoses result from a clonal disorder of keratinization. They are characterised by one or more atrophic patches surrounded by a clinically and histologically distinctive ridged hyperkeratotic border (cornoid lamella). Multiple clinical variants of porokeratosis are recognised.

Language	Label	Description	Also known as
default for all languages	ED52
English	Porokeratoses	Porokeratoses result from a clonal disorder of keratinization. They are characterised by one or more atrophic patches surrounded by a clinically and histologically distinctive ridged hyperkeratotic border (cornoid lamella). Multiple clinical variants of porokeratosis are recognised.