OMOP Concept 36714070
Syndactyly type 4
StandardConditionSNOMED719158007Disorder
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 Syndactyly type 4 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566092 | Syndactyly, Type IV | Non-standard |
| Nebraska Lexicon | 719158007 | Syndactyly type 4 | Non-standard |
Synonyms
Alternative names recorded for Syndactyly type 4 across source vocabularies.
- Haas type syndactyly
- sindactilia tipo 4
- sindactilia tipo 4 (trastorno)
- sindactilia tipo Haas
- Syndactyly type 4 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Syndactyly
- 2Autosomal hereditary disorder
- 2Congenital anomaly of digit
- 2Developmental disorder
- 2Hereditary disease
- 3Congenital anomaly of limb
- 3Disease
- 3Disorder of digit
- 3Genetic disease
- 4Clinical finding
- 4Congenital malformation
- 4Disorder of limb
- 5Congenital disease
- 5Finding of limb structure
- 6Disorder of fetus and/or newborn
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