Fragile X chromosome (Q46933): Difference between revisions
From determinar.ia.br - Determine suas informações
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| description / pt-br | description / pt-br | ||
A síndrome do X frágil é uma doença genética rara associada a déficit intelectual leve a grave que pode estar associada a transtornos comportamentais e características físicas distintas. | |||
| description / en | description / en | ||
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. | |||
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. |
