OMOP Concept 4221110
Kenny syndrome
StandardConditionSNOMED82837002Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Kenny syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136306 | Kenny Syndrome | Non-standard |
| MeSH | C537020 | Kenny-Caffey syndrome, type 2 | Non-standard |
Synonyms
Alternative names recorded for Kenny syndrome across source vocabularies.
- Kenny-Caffey syndrome
- Kenny syndrome (disorder)
- síndrome de Kenny
- síndrome de Kenny (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Idiopathic hypoparathyroidism
- 1Osteochondrodysplasia syndrome
- 2Hypoparathyroidism
- 2Idiopathic disease
- 2Multiple system malformation syndrome
- 3Congenital malformation syndrome
- 3Decreased hormone secretion
- 3Disease
- 3Disorder of parathyroid gland
- 4Clinical finding
- 4Congenital malformation
- 4Decline in functional status
- 4Disorder of endocrine system
- 4Disorder of neck
- 4Endocrine finding
- 5Congenital disease
- 5Developmental disorder
- 5Disorder of body system
- 5Finding of neck region
- 5Functional finding
- 6Fetal and/or neonatal disorder
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