Status: current, Defined. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3752705016 | Leydig cell hypoplasia | en | Synonym | Active | Case sensitive | SNOMED CT core |
794700014 | Leydig cell agenesis (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
93481014 | Leydig cell agenesis | en | Synonym | Active | Case sensitive | SNOMED CT core |
93482019 | Gonadotropin unresponsiveness syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
93483012 | Leydig cell dysgenesis | en | Synonym | Active | Case sensitive | SNOMED CT core |
93484018 | Gonadotrophin unresponsiveness syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation | Is a | True | Leydig cell agenesis | Inferred relationship | Some | |
Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation | Is a | True | Leydig cell agenesis | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set