15q24 deletion (Q101705): Difference between revisions

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@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1382727392
@@ Property / Canonical URI: https://id.who.int/icd/entity/1382727392 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1382727392
@@ Property / CURIE: CID11:ID_1382727392 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1382727392
@@ Property / Canary Token: dki-india-ID_1382727392 / 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 +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 18:32, 16 August 2026

15q24 microdeletion syndrome is a rare, recently described syndrome characterised cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.

Language	Label	Description	Also known as
default for all languages	ID_1382727392
English	15q24 deletion	15q24 microdeletion syndrome is a rare, recently described syndrome characterised cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.