ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD29 — Syndromes with obesity as a major feature
LD90.3 — Prader-Willi syndrome
ICD-11 LD90.3 — 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.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere: