| Id | Description | Lang | Type | Status | Case? | Module | 
| 3322158013 | Capra DeMarco syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | 
| 3322159017 | Capra DeMarco syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | 
| 3322160010 | Familial scaphocephaly with radioulnar synostosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 3322161014 | Berant syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core | 
| 3322162019 | Craniosynostosis, hydrocephalus, Arnold Chiari I malformation, radioulnar synostosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core | 
| 6598041000146119 | syndroom van Capra-DeMarco | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) | 
| 6598061000146118 | Capra-DeMarco-syndroom | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) | 
| 8258651000146119 | syndroom van familiale scafocefalie en radio-ulnaire synostose | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) | 
| 8258661000146116 | syndroom van craniosynostose, hydrocefalie, malformatie van Arnold-Chiari type 1 en radio-ulnaire synostose | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) | 
| 10662731000146112 | Capra-DeMarco-syndroom (aandoening) | nl | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) | 
| 3322163012 | Syndrome with characteristics of sagittal craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis. Other clinical findings include blepharophimosis, small low-set ears, hypoplastic philtrum, kidney malformation, and hypogenitalism. The syndrome was described in two brothers from a non-consanguineous family. No causative mutation has been identified so far. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |