OMOP Concept 441963
Prader-Willi syndrome
StandardConditionSNOMED89392001Disorder
Maps from
9
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
9 source codes normalize to Prader-Willi syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 113206 | Royer's Syndrome | Non-standard |
| CIEL | 129270 | Prader-Willi syndrome | Non-standard |
| ICD10CM | Q87.11 | Prader-Willi syndrome | Non-standard |
| ICD10CN | Q87.808 | Cryptorchidism - dwarf - Low smart - obesity syndrome (machine translation) | Non-standard |
| ICD9CM | 759.81 | Prader-Willi syndrome | Non-standard |
| MeSH | D011218 | Prader-Willi Syndrome | Non-standard |
| Read | PKy0.11 | Prader-Willi Syndrome | Non-standard |
| Read | PKy0.12 | Prader-Willi syndrome | Non-standard |
| Read | PKy9300 | Prader - Willi syndrome | Non-standard |
Synonyms
Alternative names recorded for Prader-Willi syndrome across source vocabularies.
- Prader Labhart Willi syndrome
- Prader-Willi syndrome (disorder)
- síndrome de Prader-Willi
- síndrome de Prader-Willi (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(43)Roll up to these when you need a wider cohort.
- 1Congenital hypogonadotropic hypogonadism
- 1Genetic syndromic childhood obesity
- 1Multiple system malformation syndrome
- 1Neurodevelopmental disorder
- 2Congenital disease
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Genetic childhood obesity disorder
- 2Hypogonadotropic hypogonadism
- 3Childhood obesity
- 3Congenital malformation
- 3Disease
- 3Disorder of anterior pituitary
- 3Fetal and/or neonatal disorder
- 3Genetic obesity disorder
- 3Hypogonadism
- 3Hypopituitarism
- 4Clinical finding
- 4Disorder of endocrine gonad
- 4Disorder of pituitary gland
- 4Genetic disease
- 4Obesity
- 5Disorder of brain
- 5Disorder of endocrine system
- 5Disorder of reproductive system
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