Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2971230015 | HNPCC - hereditary nonpolyposis colorectal cancer | en | Synonym | Active | Case sensitive | SNOMED CT core |
2971579012 | Lynch syndrome | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
459527013 | Hereditary nonpolyposis colon cancer | en | Synonym | Active | Case insensitive | SNOMED CT core |
459528015 | HNPCC - hereditary nonpolyposis colon cancer | en | Synonym | Active | Case sensitive | SNOMED CT core |
711910018 | Hereditary nonpolyposis colon cancer (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2972086014 | Autosomal dominant disease caused by a germline mutation in a DNA mismatch repair (MMR) gene and manifest by hereditary malignancy. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial colorectal cancer type X | Is a | True | Hereditary nonpolyposis colon cancer | Inferred relationship | Some | |
Family history of hereditary nonpolyposis colon cancer | Associated finding | True | Hereditary nonpolyposis colon cancer | Inferred relationship | Some | 1 |
Non-polyposis Turcot syndrome | Is a | False | Hereditary nonpolyposis colon cancer | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Neoplasm and/or hamartoma reference set
Problem/Diagnosis reference set