Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3449166014 | Hereditary skin peeling syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3449167017 | Hereditary skin peeling syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
4594936015 | Peeling skin syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
4594937012 | Familial continuous skin peeling syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Generalized peeling skin syndrome | Is a | True | Hereditary skin peeling syndrome | Inferred relationship | Existential restriction modifier | |
Acral peeling skin syndrome | Is a | True | Hereditary skin peeling syndrome | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets