Status: current, Defined. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 3722899012 | Malignant germ cell neoplasm of corpus uteri | en | Synonym | Active | Case insensitive | SNOMED CT core | 
| 3722900019 | Malignant germ cell neoplasm of corpus uteri (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core | 
| 3722901015 | Malignant germ cell tumor of corpus uteri | en | Synonym | Active | Case insensitive | SNOMED CT core | 
| 3722902010 | Malignant germ cell tumour of corpus uteri | en | Synonym | Active | Case insensitive | SNOMED CT core | 
| 3722903017 | An extremely rare uterine neoplasm with characteristics of a typically polypoid mass deriving from primordial germ cells in the endometrium. Presentation is non-specific and often includes abnormal vaginal bleeding and/or discharge, a mass protruding from the vagina, abdominal and/or pelvic pain or, less commonly, difficulty passing stool and perianal pain. The malignant teratoma and yolk sac histological subtypes are the most common. | en | Definition | Active | Case sensitive | SNOMED CT core | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Malignant germ cell neoplasm of corpus uteri | Is a | Germ cell tumour | true | Inferred relationship | Some | ||
| Malignant germ cell neoplasm of corpus uteri | Finding site | Body of uterus structure | true | Inferred relationship | Some | 1 | |
| Malignant germ cell neoplasm of corpus uteri | Associated morphology | Malignant germ cell neoplasm | true | Inferred relationship | Some | 1 | |
| Malignant germ cell neoplasm of corpus uteri | Is a | Malignant neoplasm of body of uterus | true | Inferred relationship | Some | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set