6p22 deletion (Q102063)
From determinar.ia.br - Determine suas informações
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. |
Statements
CID11:ID_1950285766
0 references
dki-india-ID_1950285766
0 references
Concluído
0 references
