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 |
| 7948801000146110 | congenitaal en/of genetisch syndroom met poikilodermie | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 7948821000146119 | congenitaal en/of genetisch syndroom met poikilodermie (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| congenitaal en/of genetisch syndroom met poikilodermie | Is a | Secondary telangiectasia (disorder) | false | Inferred relationship | Some | ||
| congenitaal en/of genetisch syndroom met poikilodermie | Is a | Poikiloderma (disorder) | false | Inferred relationship | Some | ||
| congenitaal en/of genetisch syndroom met poikilodermie | Associated morphology | Telangiectasis | false | Inferred relationship | Some | 1 | |
| congenitaal en/of genetisch syndroom met poikilodermie | Associated morphology | degeneratie (afwijkende morfologie) | false | Inferred relationship | Some | ||
| congenitaal en/of genetisch syndroom met poikilodermie | Finding site | Microscopic skin vascular structure | false | Inferred relationship | Some | 1 | |
| congenitaal en/of genetisch syndroom met poikilodermie | Is a | Congenital disease (disorder) | false | Inferred relationship | Some | ||
| congenitaal en/of genetisch syndroom met poikilodermie | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
| congenitaal en/of genetisch syndroom met poikilodermie | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
| congenitaal en/of genetisch syndroom met poikilodermie | Associated morphology | Poikiloderma | false | Inferred relationship | Some | 2 | |
| congenitaal en/of genetisch syndroom met poikilodermie | Finding site | Microscopic skin vascular structure | false | Inferred relationship | Some | 1 | |
| congenitaal en/of genetisch syndroom met poikilodermie | Associated morphology | Telangiectasis | false | Inferred relationship | Some | 1 | |
| congenitaal en/of genetisch syndroom met poikilodermie | Associated morphology | Poikiloderma | false | Inferred relationship | Some | 2 | |
| congenitaal en/of genetisch syndroom met poikilodermie | Finding site | Skin structure | false | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary sclerosing poikiloderma of Weary (disorder) | Is a | False | congenitaal en/of genetisch syndroom met poikilodermie | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
Description inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR