LD90.3 Prader-Willi syndrome
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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.
synonyms
- Prader-Willi syndrome
- Willi-Prader syndrome
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