OMOP Concept 4052211
Cockayne syndrome
StandardConditionSNOMED21086008Disorder
Maps from
5
Descendants
4
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Cockayne syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 144635 | Cockayne syndrome | Non-standard |
| MeSH | D003057 | Cockayne Syndrome | Non-standard |
| Nebraska Lexicon | 21086008 | Cockayne syndrome | Non-standard |
| Read | PKy6100 | Cockayne syndrome | Non-standard |
| Read | PKyz.11 | Cockayne's syndrome | Non-standard |
Synonyms
Alternative names recorded for Cockayne syndrome across source vocabularies.
- Cockayne syndrome (disorder)
- síndrome de Cockayne
- síndrome de Cockayne (trastorno)
- síndrome de sordera - atrofia de retina - enanismo
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.
- 1Congenital anomaly of central nervous system
- 1Developmental hereditary disorder
- 1Hereditary cancer-predisposing syndrome
- 1Hereditary disorder of nervous system
- 1Multiple malformation syndrome with senile-like appearance
- 2Congenital anomaly of nervous system
- 2Developmental disorder
- 2Disorder of nervous system
- 2Disorder of the central nervous system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 3Central nervous system finding
- 3Congenital malformation
- 3Congenital malformation syndrome
- 3Disease
- 3Disorder of body system
- 3Genetic disease
- 4Clinical finding
- 4Congenital disease
- 5Disorder of fetus and/or newborn
Narrower concepts
(4)Included automatically when you query with descendants.
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