CATCH 22 phenotype (Q39701): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-LD44.N0 | |||
| Property / Canary Token: dki-india-LD44.N0 / rank | |||
Normal rank | |||
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. |
Statements
CID11:LD44.N0
0 references
dki-india-LD44.N0
0 references
