Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3643279010 | Craniosynostosis Herrmann Opitz type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3643280013 | Craniosynostosis Herrmann Opitz type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 766331000241114 | craniosynostose de Herrmann-Opitz (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 934641000172112 | craniosynostose de Herrmann-Opitz | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3643277012 | A rare bone development disorder with characteristics of intellectual disability, short stature, turribrachycephaly, facial dysmorphism (severe hypertelorism, hypoplasia of supraorbital ridges, abnormal ears, and micrognathia), bony defects of the occiput, and digital anomalies (including syndactyly, oligodactyly, and/or brachydactyly). Urethral atresia has also been reported. There have been no further descriptions in the literature since 1987. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Craniosynostosis Herrmann Opitz type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Craniosynostosis Herrmann Opitz type (disorder) | est un(e) (attribut) | syndrome de craniosynostose (trouble) | true | Inferred relationship | Some | ||
| Craniosynostosis Herrmann Opitz type (disorder) | localisation d'une constatation (attribut) | crâne (structure corporelle) | false | Inferred relationship | Some | ||
| Craniosynostosis Herrmann Opitz type (disorder) | morphologie associée (attribut) | Congenital premature fusion | true | Inferred relationship | Some | 1 | |
| Craniosynostosis Herrmann Opitz type (disorder) | localisation d'une constatation (attribut) | Joint structure of suture of skull | true | Inferred relationship | Some | 1 | |
| Craniosynostosis Herrmann Opitz type (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR