Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Aug 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5091237016 | Human dermatosparaxis EDS VIIC (Ehlers-Danlos syndrome type 7C) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5091238014 | Dermatosparaxis Ehlers-Danlos syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5091239018 | Ehlers-Danlos syndrome type 7C | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5091240016 | Dermatosparaxis Ehlers-Danlos syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5091241017 | Dermatosparaxis EDS (Ehlers-Danlos syndrome) | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5091242012 | A form of Ehlers-Danlos syndrome (EDS) with characteristics of extreme skin fragility and laxity, a prominent facial gestalt, excessive bruising and sometimes major complications due to visceral and vascular fragility. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Is a | Ehlers-Danlos syndrome (disorder) | true | Inferred relationship | Some | ||
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Finding site | Bone structure | true | Inferred relationship | Some | 1 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 1 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Associated morphology | Dysplasia | true | Inferred relationship | Some | 2 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Finding site | Connective tissue structure | true | Inferred relationship | Some | 3 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 3 | |
Dermatosparaxis Ehlers-Danlos syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 3 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)