Prader-Willi syndrome (Q46700): Difference between revisions
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Síndrome de Prader-Willi é uma doença genética rara caracterizada por anormalidades hipotalâmico-hipofisárias com severa hipotonia durante o período neonatal e nos primeiros dois anos de vida e o aparecimento de hiperfagia com risco de obesidade mórbida durante a infância e a idade adulta, dificuldade de aprendizagem e problemas de comportamento ou problemas psiquiátricos graves. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/393773440 / rank | |||||||||||||||
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CID11:LD90.3 | |||||||||||||||
| Property / CURIE: CID11:LD90.3 / rank | |||||||||||||||
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dki-india-LD90.3 | |||||||||||||||
| Property / Canary Token: dki-india-LD90.3 / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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| Property / Linked ICD 10: CLINICA POLITANO / rank | |||||||||||||||
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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 |
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| 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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