OMOP Concept 36717526
Oculoosteocutaneous syndrome
StandardConditionSNOMED722061006Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Oculoosteocutaneous syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565893 | Brachymetapody-Anodontia-Hypotrichosis-Albinoidism | Non-standard |
| Nebraska Lexicon | 722061006 | Oculoosteocutaneous syndrome | Non-standard |
Synonyms
Alternative names recorded for Oculoosteocutaneous syndrome across source vocabularies.
- Oculoosteocutaneous syndrome (disorder)
- síndrome oculoosteocutáneo
- síndrome oculoosteocutáneo (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(63)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Ectodermal dysplasia with hair-tooth defects
- 1Hereditary disorder of the integument
- 1Hereditary disorder of tooth
- 2Autosomal hereditary disorder
- 2Congenital anomaly of hair
- 2Congenital anomaly of tooth
- 2Developmental disorder
- 2Digestive system hereditary disorder
- 2Disorder of integument
- 2Ectodermal dysplasia
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Tooth disorder
- 3Congenital abnormality of oral cavity
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of jaw
- 3Congenital anomaly of skin
- 3Congenital ectodermal defect
- 3Disease
- 3Disorder of body system
- 3Disorder of digestive organ
- 3Disorder of digestive system
- 3Disorder of hair
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