17p13.3 duplication (Q92848): Difference between revisions

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@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/288421473
@@ Property / Canonical URI: https://id.who.int/icd/entity/288421473 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_288421473
@@ Property / CURIE: CID11:ID_288421473 / rank @@
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@@ Property / Canary Token: dki-india-ID_288421473 / rank @@
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+Concluído
@@ Property / Verification Status: Concluído / rank @@
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@@ 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
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+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 07:58, 16 August 2026

17p13.3 microduplication syndrome is a chromosomal anomaly characterised by a common clinical spectrum comprising mild to moderate psychomotor delay, hypotonia and discrete craniofacial dysmorphic features including a high forehead with frontal bossing, a small nose and a small mouth.

Language	Label	Description	Also known as
default for all languages	ID_288421473
English	17p13.3 duplication	17p13.3 microduplication syndrome is a chromosomal anomaly characterised by a common clinical spectrum comprising mild to moderate psychomotor delay, hypotonia and discrete craniofacial dysmorphic features including a high forehead with frontal bossing, a small nose and a small mouth.