15q11 duplication or inversion (Q85727): Difference between revisions

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@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1920979014
@@ Property / Canonical URI: https://id.who.int/icd/entity/1920979014 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1920979014
@@ Property / CURIE: CID11:ID_1920979014 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1920979014
@@ Property / Canary Token: dki-india-ID_1920979014 / 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 11:05, 15 August 2026

The duplication/inversion 15q11 or isodicentric 15 chromosome (inv dup(15) or idic(15)) syndrome is a chromosomal disorder with distinctive clinical findings characterised by early central hypotonia, developmental delay and intellectual deficit, epilepsy, and autistic behaviour.

Language	Label	Description	Also known as
default for all languages	ID_1920979014
English	15q11 duplication or inversion	The duplication/inversion 15q11 or isodicentric 15 chromosome (inv dup(15) or idic(15)) syndrome is a chromosomal disorder with distinctive clinical findings characterised by early central hypotonia, developmental delay and intellectual deficit, epilepsy, and autistic behaviour.