OMOP Concept 36717429
Frank-Ter Haar syndrome
StandardConditionSNOMED720958002Disorder
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 Frank-Ter Haar syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537274 | Ter Haar syndrome | Non-standard |
Synonyms
Alternative names recorded for Frank-Ter Haar syndrome across source vocabularies.
- Frank-Ter Haar syndrome (disorder)
- síndrome de Frank-Ter-Haar
- síndrome de Frank-Ter-Haar (trastorno)
- Ter Haar syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(53)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Congenital anomaly of skeletal bone
- 1Developmental delay
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary disorder of the visual system
- 1Lesion of bone
- 1Megalocornea
- 1Multiple malformation syndrome with facial defects as major feature
- 1Skeletal dysplasia
- 2Autosomal hereditary disorder
- 2Congenital anomaly of face
- 2Congenital anomaly of musculoskeletal system
- 2Congenital structural abnormality of cornea
- 2Developmental disorder
- 2Disorder of bone
- 2Disorder of bone development
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
- 2Structural abnormality of skeleton
- 2Visual system disorder
- 3Bone finding
- 3Congenital anomaly of anterior segment of eye
Showing 25 of 53. Retrieve the full set via the API.
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