OMOP Concept 36715271
Capra DeMarco syndrome
StandardConditionSNOMED720815000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Capra DeMarco syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 720815000 | Familial scaphocephaly with radioulnar synostosis syndrome | Non-standard |
Synonyms
Alternative names recorded for Capra DeMarco syndrome across source vocabularies.
- Berant syndrome
- Capra DeMarco syndrome (disorder)
- Craniosynostosis, hydrocephalus, Arnold Chiari I malformation, radioulnar synostosis
- Familial scaphocephaly with radioulnar synostosis syndrome
- síndrome de Berant
- síndrome de Capra DeMarco
- síndrome de Capra DeMarco (trastorno)
- síndrome de escafocefalia familiar con sinostosis radiocubital
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(62)Roll up to these when you need a wider cohort.
- 1Chiari malformation type I
- 1Congenital anomaly of bone and joint
- 1Congenital hydrocephalus
- 1Congenital radioulnar synostosis
- 1Craniosynostosis syndrome
- 1Genetic disease
- 1Multiple malformation syndrome with limb defect as major feature
- 2Chiari malformation
- 2Congenital abnormal fusion of radius
- 2Congenital abnormal fusion of ulna
- 2Congenital anomaly of brain
- 2Congenital anomaly of joint
- 2Congenital anomaly of skeletal bone
- 2Disease
- 2Failure of differentiation of bones of forearm
- 2Hydrocephalus
- 2Imperfect fusion of skull
- 2Multiple system malformation syndrome
- 2Radioulnar synostosis
- 3Arthropathy
- 3Cerebellar hernia
- 3Clinical finding
- 3Congenital anomaly of central nervous system
- 3Congenital anomaly of head
- 3Congenital anomaly of musculoskeletal system
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