Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770693017 | Congenital/genetic syndrome with poikiloderma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1781863011 | Congenital/genetic syndrome with poikiloderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 707981000077112 | poïkilodermie avec syndrome génétique ou congénital (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 85191000077116 | poïkilodermie avec syndrome génétique ou congénital | 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 |
| Hereditary sclerosing poikiloderma of Weary (disorder) | est un(e) (attribut) | False | Congenital/genetic syndrome with poikiloderma (disorder) | Inferred relationship | Some |
Reference Sets
Canada English language reference set (foundation metadata concept)
Concept inactivation indicator reference set
Description inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR