OMOP Concept 35622011
Craniofaciofrontodigital syndrome
StandardConditionSNOMED763320005Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Craniofaciofrontodigital syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C567298 | Craniofaciofrontodigital Syndrome | Non-standard |
Synonyms
Alternative names recorded for Craniofaciofrontodigital syndrome across source vocabularies.
- Cantu craniofaciofrontodigital syndrome
- Craniofaciofrontodigital syndrome (disorder)
- síndrome craneofaciofrontodigital
- síndrome craneofaciofrontodigital (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(73)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of skin
- 1Cutis laxa
- 1Dysostosis of bone of skull
- 1Genetic intellectual disability
- 1Metabolic bone disease
- 1Multiple malformation syndrome with facial defects as major feature
- 1Musculoskeletal and connective tissue disorder
- 1Short stature disorder
- 2Collagen and elastic tissue disorders affecting skin
- 2Congenital anomaly of face
- 2Congenital anomaly of integument
- 2Congenital anomaly of skull
- 2Disorder of bone
- 2Disorder of connective tissue
- 2Disorder of musculoskeletal system
- 2Disorder of skin
- 2Disorder of stature
- 2Dysostosis
- 2Genetic disease
- 2Intellectual disability
- 2Metabolic disease
- 2Metabolic disease of collagen
- 2Multiple system malformation syndrome
- 2Short stature
- 3Abnormal behavior
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