OMOP Concept 36716167
Oro-facial digital syndrome type 10
StandardConditionSNOMED722075004Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to Oro-facial digital syndrome type 10 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563491 | Orofaciodigital Syndrome X | Non-standard |
| Nebraska Lexicon | 722075004 | Orofaciodigital syndrome with fibular aplasia | Non-standard |
Synonyms
Alternative names recorded for Oro-facial digital syndrome type 10 across source vocabularies.
- Figuera syndrome
- Oro-facial digital syndrome type 10 (disorder)
- Orofaciodigital syndrome type 10
- Orofaciodigital syndrome with fibular aplasia
- síndrome de Figuera
- síndrome orofacial digital tipo 10
- síndrome orofacial digital tipo 10 (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.
- 1Intellectual disability
- 1Oral-facial-digital syndrome
- 2Behavior finding
- 2Congenital abnormality of oral cavity
- 2Congenital anomaly of digit
- 2Ectodermal dysplasia
- 2Genetic disease
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Multiple malformation syndrome with facial-limb defects as major feature
- 2Neurodevelopmental disorder
- 3Cognitive function finding
- 3Congenital anomaly of limb
- 3Congenital anomaly of mouth
- 3Congenital ectodermal defect
- 3Developmental disorder
- 3Disease
- 3Disorder of digit
- 3Genodermatosis
- 3Intelligence finding
- 3Mental state, behavior and/or psychosocial function finding
- 3Multiple malformation syndrome with facial defects as major feature
- 3Multiple malformation syndrome with limb defect as major feature
- 3Oral cavity finding
- 4Clinical finding
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