Deletions of the short arm of chromosome 11 (Q46877): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Essas deleções podem dar origem à síndrome de Paris-Trousseau, um transtorno muito raro em que déficit intelectual, malformações cardíacas e anormalidades faciais estão associados a trombocitopenia e dismegacariopoiese.
@@ description / en / description / en @@
+These deletions may give rise to the Paris-Trousseau syndrome, a very rare disorder in which intellectual deficit, cardiac malformations and facial abnormalities are associated with thrombocytopenia and dysmegakaryopoiesis.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/127054483
@@ Property / Canonical URI: https://id.who.int/icd/entity/127054483 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD44.B1
@@ Property / CURIE: CID11:LD44.B1 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD44.B1
@@ Property / Canary Token: dki-india-LD44.B1 / 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 @@
+STEPHANY OLIVEIRA BASTOS
@@ Property / Linked ICD 10: STEPHANY OLIVEIRA BASTOS / rank @@
+Normal rank

Latest revision as of 15:44, 13 August 2026

These deletions may give rise to the Paris-Trousseau syndrome, a very rare disorder in which intellectual deficit, cardiac malformations and facial abnormalities are associated with thrombocytopenia and dysmegakaryopoiesis.

Language	Label	Description	Also known as
default for all languages	LD44.B1
English	Deletions of the short arm of chromosome 11	These deletions may give rise to the Paris-Trousseau syndrome, a very rare disorder in which intellectual deficit, cardiac malformations and facial abnormalities are associated with thrombocytopenia and dysmegakaryopoiesis.