2q32q33 deletion (Q60201): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A síndrome de microdeleção 2q32q33 é uma anomalia cromossômica associada a um fenótipo variável envolvendo déficit intelectual moderado a grave, atraso significativo na fala, dificuldades persistentes de alimentação, retardo de crescimento e características dismórficas.
@@ description / en / description / en @@
+q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/2015922071
@@ Property / Canonical URI: https://id.who.int/icd/entity/2015922071 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_2015922071
@@ Property / CURIE: CID11:ID_2015922071 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_2015922071
@@ Property / Canary Token: dki-india-ID_2015922071 / 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 07:42, 14 August 2026

2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features.

Language	Label	Description	Also known as
default for all languages	ID_2015922071
English	2q32q33 deletion	2q32q33 microdeletion syndrome is a chromosomal anomaly associated with a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features.