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 |
| 1770665016 | Skin damage resulting from congenital/hereditary neuropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 1781838011 | Skin damage resulting from congenital/hereditary neuropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Skin damage resulting from congenital/hereditary neuropathy (disorder) | Due to | atteinte d'un nerf périphérique | false | Inferred relationship | Some | 1 | |
| Skin damage resulting from congenital/hereditary neuropathy (disorder) | est un(e) (attribut) | Dermatosis secondary to peripheral nerve disorder | false | Inferred relationship | Some | ||
| Skin damage resulting from congenital/hereditary neuropathy (disorder) | localisation d'une constatation (attribut) | structure de la peau | false | Inferred relationship | Some | 2 | |
| Skin damage resulting from congenital/hereditary neuropathy (disorder) | est un(e) (attribut) | Congenital disease | false | Inferred relationship | Some | ||
| Skin damage resulting from congenital/hereditary neuropathy (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | ||
| Skin damage resulting from congenital/hereditary neuropathy (disorder) | associé à (attribut) | atteinte d'un nerf périphérique | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR