OMOP Concept 36675012
Pilodental dysplasia, refractive errors syndrome
StandardConditionSNOMED771240009Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2019
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Pilodental dysplasia, refractive errors syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535763 | Euhidrotic ectodermal dysplasia | Non-standard |
Synonyms
Alternative names recorded for Pilodental dysplasia, refractive errors syndrome across source vocabularies.
- Euhidrotic ectodermal dysplasia
- Kopysc Barczyk Krol syndrome
- Pilodental dysplasia, refractive errors syndrome (disorder)
- síndrome de displasia pilodental y errores de refracción
- síndrome de displasia pilodental y errores de refracción (trastorno)
- síndrome de Kopysc Barczyk Krol
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(70)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Developmental hereditary disorder
- 1Disorder of refraction
- 1Ectodermal dysplasia with hair-tooth defects
- 1Hereditary disorder of the integument
- 1Hereditary disorder of the visual system
- 1Hereditary disorder of tooth
- 2Autosomal hereditary disorder
- 2Congenital anomaly of hair
- 2Congenital anomaly of tooth
- 2Developmental disorder
- 2Digestive system hereditary disorder
- 2Disorder of integument
- 2Disorder of refraction AND/OR accommodation
- 2Ectodermal dysplasia
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Tooth disorder
- 2Visual system disorder
- 3Congenital abnormality of oral cavity
- 3Congenital anomaly of digestive organ
- 3Congenital anomaly of jaw
- 3Congenital anomaly of skin
- 3Congenital ectodermal defect
- 3Disease
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