Prader-Willi syndrome (Q46700): Difference between revisions
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13 August 2026
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Latest revision as of 15:28, 13 August 2026
Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioural problems or severe psychiatric problems.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD90.3 |
||
| English | Prader-Willi syndrome |
Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behavioural problems or severe psychiatric problems. |
Statements
CID11:LD90.3
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dki-india-LD90.3
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Concluído
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13 August 2026
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