Fragile X chromosome (Q46933): Difference between revisions
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Revision as of 15:50, 13 August 2026
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. |
Statements
CID11:LD55
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