Fragile X chromosome (Q46933)

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.