Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
13786011 | Autosomal dominant hypohidrotic ectodermal dysplasia syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
13787019 | Rapp-Hodgkin ectodermal dysplasia syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
503512017 | Anhidrotic ectodermal dysplasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
503513010 | Rapp-Hodgkin type of ectodermal dysplasia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
503514016 | Hypohidrotic ectodermal dysplasia | en | Synonym | Inactive | Entire term case insensitive | SNOMED CT core module |
503515015 | Anhidrotic ectodermal dysplasia syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
503516019 | Hypohidrotic ectodermal dysplasia syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
818127016 | Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hypohidrotic X-linked ectodermal dysplasia | Is a | False | Autosomal dominant hypohidrotic ectodermal dysplasia syndrome | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets