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