6p22 deletion (Q102063): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A síndrome de microdeleção 6p22 é uma anomalia cromossômica associada a um fenótipo clínico variável, incluindo atraso no desenvolvimento, dismorfismo facial, pescoço curto e malformações diversas. | |||
| description / en | description / en | ||
6p22 microdeletion syndrome is a chromosomal anomaly associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations. | |||
Revision as of 18:56, 16 August 2026
6p22 microdeletion syndrome is a chromosomal anomaly associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1950285766 |
||
| English | 6p22 deletion |
6p22 microdeletion syndrome is a chromosomal anomaly associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations. |
