OMOP Concept 4252383
Barber-Say syndrome
StandardConditionSNOMED408537003Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2004
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to Barber-Say syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537908 | Barber Say syndrome | Non-standard |
| Nebraska Lexicon | 408537003 | Barber-Say syndrome | Non-standard |
| Read | PKyE.00 | Barber-Say syndrome | Non-standard |
Synonyms
Alternative names recorded for Barber-Say syndrome across source vocabularies.
- Barber-Say syndrome (disorder)
- síndrome de Barber-Say
- síndrome de Barber-Say (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(55)Roll up to these when you need a wider cohort.
- 1Atrophic condition of skin
- 1Congenital hypertrichosis
- 1Ectodermal dysplasia
- 1Genetic disease
- 1Microstomia
- 1Multiple malformation syndrome with facial defects as major feature
- 2Congenital anomaly of face
- 2Congenital anomaly of hair
- 2Congenital anomaly of mouth
- 2Congenital ectodermal defect
- 2Degenerative skin disorder
- 2Disease
- 2Genodermatosis
- 2Hypertrichosis
- 2Multiple system malformation syndrome
- 3Clinical finding
- 3Congenital anomaly of head
- 3Congenital anomaly of skin
- 3Congenital malformation
- 3Congenital malformation of upper alimentary tract
- 3Congenital malformation syndrome
- 3Degenerative disorder
- 3Disease of mouth
- 3Disorder of embryonic structure
- 3Disorder of face
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