Genetic syndromes with poikiloderma (Q44243): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Síndromes hereditárias em que a poiquilodermia (pigmentação cutânea, atrofia e telangiectasias) é uma característica notável.
@@ description / en / description / en @@
+Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1343350087
@@ Property / Canonical URI: https://id.who.int/icd/entity/1343350087 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:EC10
@@ Property / CURIE: CID11:EC10 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-EC10
@@ Property / Canary Token: dki-india-EC10 / 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 @@
+L99.8
@@ Property / Linked ICD 10: L99.8 / rank @@
+Normal rank

Latest revision as of 11:38, 13 August 2026

Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature.

Language	Label	Description	Also known as
default for all languages	EC10
English	Genetic syndromes with poikiloderma	Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature.