1p36 deletion (Q105605): Difference between revisions

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@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1248053946
@@ Property / Canonical URI: https://id.who.int/icd/entity/1248053946 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1248053946
@@ Property / CURIE: CID11:ID_1248053946 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1248053946
@@ Property / Canary Token: dki-india-ID_1248053946 / 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 +2026-08-16T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-16T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 16 August 2026 / rank @@
+Normal rank

Latest revision as of 11:56, 17 August 2026

Monosomy 1p36 is a distinct chromosome deletion syndrome characterised by usually severe developmental delay, behavioural difficulties and self-injury, hypotonia and feeding problems with oropharyngeal dysphagia are frequent, and seizures. Other dysmorphic, cardiac, visual and auditive features have been described.

Language	Label	Description	Also known as
default for all languages	ID_1248053946
English	1p36 deletion	Monosomy 1p36 is a distinct chromosome deletion syndrome characterised by usually severe developmental delay, behavioural difficulties and self-injury, hypotonia and feeding problems with oropharyngeal dysphagia are frequent, and seizures. Other dysmorphic, cardiac, visual and auditive features have been described.