OMOP Concept 36713733
Oro-facial digital syndrome type 9
StandardConditionSNOMED718680001Disorder
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 Oro-facial digital syndrome type 9 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C557818 | Orofaciodigital syndrome 9 | Non-standard |
| Nebraska Lexicon | 718680001 | Orofaciodigital syndrome with retinal abnormality | Non-standard |
Synonyms
Alternative names recorded for Oro-facial digital syndrome type 9 across source vocabularies.
- Oral-facial-digital syndrome type 9
- Oro-facial digital syndrome type 9 (disorder)
- Orofaciodigital syndrome type 9
- Orofaciodigital syndrome with retinal abnormality
- síndrome orofaciodigital tipo 9
- síndrome orofaciodigital tipo 9 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(86)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of retina
- 1Developmental hereditary disorder
- 1Digestive system hereditary disorder
- 1Hereditary disorder of the integument
- 1Hereditary disorder of the visual system
- 1Intellectual disability
- 1Oral-facial-digital syndrome
- 2Autosomal hereditary disorder
- 2Behavior finding
- 2Congenital abnormality of oral cavity
- 2Congenital anomaly of digit
- 2Congenital anomaly of posterior segment of eye
- 2Developmental disorder
- 2Disorder of digestive system
- 2Disorder of integument
- 2Ectodermal dysplasia
- 2Genetic disease
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Multiple malformation syndrome with facial-limb defects as major feature
- 2Neurodevelopmental disorder
- 2Retinal disorder
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