Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3499490015 | Hereditary anetoderma (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3499491016 | Hereditary macular atrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3499492011 | Hereditary anetoderma | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3500008013 | An extremely rare genetic skin disease characterised by loss of elastin tissue leading to localised areas of flaccid skin and a family history of the disorder. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3500009017 | An extremely rare genetic skin disease characterized by loss of elastin tissue leading to localized areas of flaccid skin and a family history of the disorder. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary anetoderma (disorder) | morphologie associée (attribut) | Focal atrophy | true | Inferred relationship | Some | 1 | |
| Hereditary anetoderma (disorder) | est un(e) (attribut) | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Hereditary anetoderma (disorder) | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
| Hereditary anetoderma (disorder) | est un(e) (attribut) | Anetoderma | true | Inferred relationship | Some | ||
| Hereditary anetoderma (disorder) | est un(e) (attribut) | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Hereditary anetoderma (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 | |
| Hereditary anetoderma (disorder) | localisation d'une constatation (attribut) | structure de la peau | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR