8p11.2 deletion (Q101715): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A síndrome de deleção 8p11.2 é uma síndrome de gene contíguo caracterizada pela associação de esferocitose congênita, características dismórficas, retardo de crescimento e hipogonadismo hipogonadotrópico.
@@ description / en / description / en @@
+p11.2 deletion syndrome is a contiguous gene syndrome characterised by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.
@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1782338750
@@ Property / Canonical URI: https://id.who.int/icd/entity/1782338750 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1782338750
@@ Property / CURIE: CID11:ID_1782338750 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1782338750
@@ Property / Canary Token: dki-india-ID_1782338750 / 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 18:33, 16 August 2026

8p11.2 deletion syndrome is a contiguous gene syndrome characterised by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.

Language	Label	Description	Also known as
default for all languages	ID_1782338750
English	8p11.2 deletion	8p11.2 deletion syndrome is a contiguous gene syndrome characterised by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.