Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3310447015 | Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3310448013 | Cerebro-oculo-dento-auriculo-skeletal syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3310513016 | CODAS syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3310514010 | CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401590018 | Codas syndrome is a multiple congenital anomalies syndrome characterized by Cerebral, Ocular, Dental, Auricular and Skeletal anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5401591019 | Codas syndrome is a multiple congenital anomalies syndrome characterised by Cerebral, Ocular, Dental, Auricular and Skeletal anomalies. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
| Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 1 | |
| Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
| Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR