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 |
3431530019 | Lipodystrophy due to peptidic growth factors deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3431531015 | Lipodystrophy due to peptidic growth factors deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3431532010 | Combined insulin, insulin-like growth factor 1 and epidermal growth factor deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3431533017 | Hoepffner Dreyer Reimers syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
3431534011 | Werner-like syndrome due to combined growth factor deficiency | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Lipodystrophy due to peptidic growth factors deficiency | Is a | Lipodystrophy | true | Inferred relationship | Existential restriction modifier | ||
Lipodystrophy due to peptidic growth factors deficiency | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 2 | |
Lipodystrophy due to peptidic growth factors deficiency | Finding site | Structure of subcutaneous fatty tissue | true | Inferred relationship | Existential restriction modifier | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets