OMOP Concept 4300851
Baller-Gerold syndrome
StandardConditionSNOMED77608001Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Baller-Gerold syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 147984 | Baller-Gerold syndrome | Non-standard |
| MeSH | C536788 | Craniosynostosis radial aplasia syndrome | Non-standard |
Synonyms
Alternative names recorded for Baller-Gerold syndrome across source vocabularies.
- Baller-Gerold syndrome (disorder)
- Craniosynostosis-radial aplasia syndrome
- síndrome de Baller - Gerold
- síndrome de Baller - Gerold (trastorno)
- síndrome de craneosinostosis - aplasia radial
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 bone and joint
- 1Congenital dysplasia of radius
- 1Craniosynostosis syndrome
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 2Autosomal hereditary disorder
- 2Congenital anomaly of joint
- 2Congenital anomaly of radius
- 2Congenital anomaly of skeletal bone
- 2Congenital dysplasia of limb
- 2Developmental disorder
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Imperfect fusion of skull
- 2Lesion of bone
- 2Skeletal dysplasia
- 3Arthropathy
- 3Congenital anomaly of head
- 3Congenital anomaly of limb
- 3Congenital anomaly of musculoskeletal system
- 3Congenital anomaly of upper limb
- 3Cranial suture finding
- 3Disease
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