OMOP Concept 36716127
Isotretinoin-like syndrome
StandardConditionSNOMED722006004Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Isotretinoin-like syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535542 | Isotretinoin embryopathy like syndrome | Non-standard |
Synonyms
Alternative names recorded for Isotretinoin-like syndrome across source vocabularies.
- Isotretinoin embryopathy-like syndrome
- Isotretinoin embryopathy-like syndrome (disorder)
- Kawashima syndrome
- Microtia aortic arch syndrome
- síndrome de Kawashima
- síndrome similar a la embriopatía por isotretinoína
- síndrome similar a la embriopatía por isotretinoína (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(78)Roll up to these when you need a wider cohort.
- 1Auditory system hereditary disorder
- 1Cardiovascular system hereditary disorder
- 1Congenital anomaly of aortic arch
- 1Congenital anomaly of central nervous system
- 1Developmental hereditary disorder
- 1Hereditary disorder of nervous system
- 1Microtia
- 1Multiple malformation syndrome with facial defects as major feature
- 2Abnormality of aortic arch
- 2Congenital abnormality of external ear
- 2Congenital anomaly of aorta
- 2Congenital anomaly of face
- 2Congenital anomaly of nervous system
- 2Congenital anomaly of thorax
- 2Developmental disorder
- 2Disorder of auditory system
- 2Disorder of cardiovascular system
- 2Disorder of nervous system
- 2Disorder of the central nervous system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 3Cardiovascular finding
- 3Central nervous system finding
- 3Congenital abnormality of systemic artery
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