1q21.1 deletion (Q59705): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/1854309838 / rank | |||
Normal rank | |||
Revision as of 07:13, 14 August 2026
1q21.1 microdeletion syndrome is a recurrent deletion syndrome with variable clinical manifestations including variable intellectual deficit and facial dysmorphism, but without the clinical picture of thrombocytopenia - absent radius (TAR) syndrome, which is also caused by 1q21.1 deletions.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1854309838 |
||
| English | 1q21.1 deletion |
1q21.1 microdeletion syndrome is a recurrent deletion syndrome with variable clinical manifestations including variable intellectual deficit and facial dysmorphism, but without the clinical picture of thrombocytopenia - absent radius (TAR) syndrome, which is also caused by 1q21.1 deletions. |
