Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 132153018 | Anomaly of chromosome pair 19 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 469771000241114 | anomalie du chromosome 19 (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 820730015 | Anomaly of chromosome pair 19 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 922911000172113 | anomalie du chromosome 19 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| 19q partial trisomy syndrome | est un(e) (attribut) | False | Anomaly of chromosome pair 19 | Inferred relationship | Some | |
| 19p13.12 microdeletion syndrome (disorder) | est un(e) (attribut) | False | Anomaly of chromosome pair 19 | Inferred relationship | Some | |
| 19q13.11 microdeletion syndrome (disorder) | est un(e) (attribut) | False | Anomaly of chromosome pair 19 | Inferred relationship | Some | |
| Deletion of part of chromosome 19 (disorder) | est un(e) (attribut) | True | Anomaly of chromosome pair 19 | Inferred relationship | Some | |
| Partial trisomy of chromosome 19 | est un(e) (attribut) | True | Anomaly of chromosome pair 19 | Inferred relationship | Some | |
| Ring chromosome 19 syndrome | est un(e) (attribut) | True | Anomaly of chromosome pair 19 | Inferred relationship | Some |
This concept is not in any reference sets
FHIR