CATCH 22 phenotype (Q39701): Difference between revisions

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@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1868156761
@@ Property / Canonical URI: https://id.who.int/icd/entity/1868156761 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:LD44.N0
@@ Property / CURIE: CID11:LD44.N0 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-LD44.N0
@@ Property / Canary Token: dki-india-LD44.N0 / 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
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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
@@ Property / Linked ICD 10 @@
+D82.1
@@ Property / Linked ICD 10: D82.1 / rank @@
+Normal rank

Latest revision as of 05:13, 13 August 2026

Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal heart defects, a subtle but characteristic facial dysmorphism, cleft palate or velar insufficiency, and learning difficulties.

Language	Label	Description	Also known as
default for all languages	LD44.N0
English	CATCH 22 phenotype	Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal heart defects, a subtle but characteristic facial dysmorphism, cleft palate or velar insufficiency, and learning difficulties.