Complete trisomy 18 (Q46806): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A trissomia 18 é uma anormalidade cromossômica associada à presença de um cromossomo 18 extra e caracterizada por atraso no crescimento, dolicocefalia, uma fácies característica, anomalias de membros e malformações viscerais.
@@ description / en / description / en @@
+Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterised by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1505179968
@@ Property / Canonical URI: https://id.who.int/icd/entity/1505179968 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD40.2
@@ Property / CURIE: CID11:LD40.2 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD40.2
@@ Property / Canary Token: dki-india-LD40.2 / 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 @@
+Q91.3
@@ Property / Linked ICD 10: Q91.3 / rank @@
+Normal rank

Latest revision as of 15:37, 13 August 2026

Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterised by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations.

Language	Label	Description	Also known as
default for all languages	LD40.2
English	Complete trisomy 18	Trisomy 18 is a chromosomal abnormality associated with the presence of an extra chromosome 18 and characterised by growth delay, dolichocephaly, a characteristic facies, limb anomalies and visceral malformations.