Fragile X chromosome (Q46933)
From determinar.ia.br - Determine suas informações
Fragile X syndrome is a rare genetic disease associated with mild to severe intellectual deficit that may be associated with behavioural disorders and characteristic physical features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD55 |
||
| English | Fragile X chromosome |
Fragile X syndrome is a rare genetic disease associated with mild to severe intellectual deficit that may be associated with behavioural disorders and characteristic physical features. |
