Poikiloderma (Q62989): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Poiquilodermia é definida como uma combinação de atrofia da pele, pigmentação e telangiectasias. É um componente de uma série de síndromes genéticas, de determinados transtornos autoimunes sistêmicos não específicos de órgãos, e pode ocorrer subsequente a lesão na pele, incluindo por radioterapia.
@@ description / en / description / en @@
+Poikiloderma is defined as a combination of skin atrophy, pigmentation and telangiectasia. It is a component of a number of genetic syndromes, of certain non-organ-specific systemic autoimmune disorders and may follow skin injury including from radiotherapy.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/657613175
@@ Property / Canonical URI: https://id.who.int/icd/entity/657613175 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_657613175
@@ Property / CURIE: CID11:ID_657613175 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_657613175
@@ Property / Canary Token: dki-india-ID_657613175 / 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

Latest revision as of 10:28, 14 August 2026

Poikiloderma is defined as a combination of skin atrophy, pigmentation and telangiectasia. It is a component of a number of genetic syndromes, of certain non-organ-specific systemic autoimmune disorders and may follow skin injury including from radiotherapy.

Language	Label	Description	Also known as
default for all languages	ID_657613175
English	Poikiloderma	Poikiloderma is defined as a combination of skin atrophy, pigmentation and telangiectasia. It is a component of a number of genetic syndromes, of certain non-organ-specific systemic autoimmune disorders and may follow skin injury including from radiotherapy.