OMOP Concept 36715123
Cardiospondylocarpofacial syndrome
StandardConditionSNOMED720612000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
1 source code normalizes to Cardiospondylocarpofacial syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537269 | Forney Robinson Pascoe syndrome | Non-standard |
Synonyms
Alternative names recorded for Cardiospondylocarpofacial syndrome across source vocabularies.
- Cardiospondylocarpofacial syndrome (disorder)
- Forney Robinson Pascoe syndrome
- Forney syndrome
- Mitral regurgitation with deafness and skeletal anomalies syndrome
- síndrome cardioespondilocarpofacial
- síndrome cardioespondilocarpofacial (trastorno)
- síndrome de Forney-Robinson-Pascoe
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(91)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Cardiovascular system hereditary disorder
- 1Conductive hearing loss
- 1Congenital anomaly of ear with impairment of hearing
- 1Congenital anomaly of skeletal bone
- 1Congenital insufficiency of mitral valve
- 1Developmental hereditary disorder
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary hearing loss
- 1Multiple system malformation syndrome
- 1Short stature disorder
- 2Auditory system hereditary disorder
- 2Autosomal hereditary disorder
- 2Congenital anomaly of mitral valve
- 2Congenital anomaly of musculoskeletal system
- 2Congenital hearing disorder
- 2Congenital malformation of ear
- 2Congenital malformation syndrome
- 2Congenital valvular insufficiency
- 2Developmental disorder
- 2Disorder of bone development
- 2Disorder of cardiovascular system
- 2Disorder of ear
- 2Disorder of musculoskeletal system
- 2Disorder of stature
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