OMOP Concept 4113731
Singleton-Merten syndrome
StandardConditionSNOMED254114000Disorder
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 Singleton-Merten syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 158822 | Singleton-Merten syndrome | Non-standard |
| MeSH | C537343 | Singleton Merten syndrome | Non-standard |
Synonyms
Alternative names recorded for Singleton-Merten syndrome across source vocabularies.
- síndrome de Sigleon-Merten
- síndrome de Sigleon-Merten (trastorno)
- Singleton-Merten syndrome (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(45)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Developmental hereditary disorder
- 1Dysplasia with decreased bone density
- 1Hereditary disorder of immune system
- 1Hereditary disorder of musculoskeletal system
- 1Type I interferonopathy
- 2Autosomal hereditary disorder
- 2Bone density below reference range
- 2Congenital anomaly of skeletal bone
- 2Developmental disorder
- 2Disorder of immune function
- 2Disorder of musculoskeletal system
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Lesion of bone
- 2Monogenic autoinflammatory syndrome
- 2Skeletal dysplasia
- 3Autoinflammatory disease
- 3Bone densimetry abnormal
- 3Bone density finding
- 3Congenital anomaly of musculoskeletal system
- 3Disease
- 3Disorder of body system
- 3Disorder of bone
- 3Disorder of bone development
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