Prader-Willi syndrome

ICD-11 code : LD90.3;

Preferred Label : Prader-Willi syndrome;

ICD-11 definition : Prader-Willi syndrome is a rare genetic disorder characterized 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 behavioral problems or severe psychiatric problems.;

ICD-11 synonym : Willi-Prader syndrome;

Details

Origin ID

393773440;

Currated CISMeF NLP mapping
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category]
- Prader Willi syndrome [Disease (Nov.)]
- Prader-Labhart-Willi syndrome [PASCAL descriptor]
- Prader-Willi Syndrome [NCIt concept]
- Prader-Willi syndrome [DO Concept]
- Prader-Willi syndrome [MeSH concept]
- Prader-Willi syndrome [ICD-9 code]
- Prader-Willi syndrome [ORDO Disease]
- Prader-Willi syndrome [MedDRA Preferred Term]
- Prader-Willi syndrome (disorder) [SNOMED CT concept]
- Prader-willi syndrome [OMIM Phenotype]
- prader-willi syndrome [MeSH Descriptor]
- prader-willi syndrome [MedlinePlus Topic]
- prader-willi syndrome [SNOMED Notion]
ICD-10 Mapping
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category]
Validated automatic mappings to NTBT
- Congenital malformation syndromes associated with short stature (disorder) [SNOMED CT concept]

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