Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 7920012 | Robin sequence | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 7921011 | Micrognathia-glossoptosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 7922016 | Pierre Robin syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 783324010 | Robin sequence (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 1230294017 | Pierre Robin association | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 2598851000052112 | Pierre Robins syndrom | sv | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Robin sequence | Is a | Multisystem disorder O-P | false | Inferred relationship | Some | ||
| Robin sequence | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
| Robin sequence | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Robin sequence | Associated morphology | medfödd missbildning | false | Inferred relationship | Some | ||
| Robin sequence | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Robin sequence | Associated morphology | utvecklingsabnormitet | false | Inferred relationship | Some | 1 | |
| Robin sequence | Finding site | Face structure | true | Inferred relationship | Some | 1 | |
| Robin sequence | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Robin sequence | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome (disorder) | Is a | True | Robin sequence | Inferred relationship | Some | |
| Pierre Robin sequence faciodigital anomaly syndrome (disorder) | Is a | True | Robin sequence | Inferred relationship | Some | |
| Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome (disorder) | Is a | True | Robin sequence | Inferred relationship | Some | |
| Intellectual disability, brachydactyly, Pierre Robin syndrome (disorder) | Is a | True | Robin sequence | Inferred relationship | Some | |
| Robin sequence and oligodactyly syndrome | Is a | True | Robin sequence | Inferred relationship | Some | |
| Joint contractures, developmental delay, Pierre Robin syndrome (disorder) | Is a | True | Robin sequence | Inferred relationship | Some |
This concept is not in any reference sets
FHIR