Status: current, Not sufficiently defined by necessary conditions definition status. Date: 28-Feb 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 4695998013 | Familial colorectal cancer type X (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module | 
| 4695999017 | Familial colorectal cancer type X | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module | 
| 4696000015 | FCCTX - familial colorectal cancer type X | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Familial colorectal cancer type X | Is a | Hereditary nonpolyposis colon cancer | true | Inferred relationship | Existential restriction modifier | ||
| Familial colorectal cancer type X | Finding site | Colon structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial colorectal cancer type X | Associated morphology | Malignant neoplasm, primary | false | Inferred relationship | Existential restriction modifier | 1 | |
| Familial colorectal cancer type X | Associated morphology | Malignant neoplasm | true | Inferred relationship | Existential restriction modifier | 1 | |
| Familial colorectal cancer type X | Pathological process | Malignant proliferation of primary neoplasm | true | Inferred relationship | Existential restriction modifier | 1 | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
This concept is not in any reference sets