OMOP Concept 36715002
Acropectorovertebral dysplasia
StandardConditionSNOMED720457000Disorder
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 Acropectorovertebral dysplasia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C566319 | Acropectorovertebral Dysplasia, F-Form | Non-standard |
| Nebraska Lexicon | 720457000 | Acropectorovertebral dysplasia | Non-standard |
Synonyms
Alternative names recorded for Acropectorovertebral dysplasia across source vocabularies.
- Acropectorovertebral dysplasia (disorder)
- displasia acropectorovertebral
- displasia acropectorovertebral (trastorno)
- F syndrome
- síndrome F
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(59)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Congenital anomaly of digit
- 1Congenital anomaly of spine
- 1Congenital malformation of sternum
- 1Developmental hereditary disorder
- 1Disorder of vertebral column
- 1Dysostosis
- 1Hereditary disorder of musculoskeletal system
- 1Multiple malformation syndrome with limb defect as major feature
- 2Autosomal hereditary disorder
- 2Congenital anomaly of body wall
- 2Congenital anomaly of limb
- 2Congenital anomaly of skeletal bone
- 2Congenital anomaly of thoracic cage
- 2Congenital anomaly of vertebral region of back
- 2Congenital malformation of bone of thorax
- 2Developmental disorder
- 2Disorder of digit
- 2Disorder of musculoskeletal system
- 2Disorder of skeletal system
- 2Disorder of spinal region
- 2Finding of sternum structure
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Multiple system malformation syndrome
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