Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3642783018 | Serrated polyposis | en | Synonym | Active | Case insensitive | SNOMED CT core |
3642784012 | Hyperplastic polyposis syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3642785013 | Hyperplastic polyposis syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3642786014 | A rare genetic intestinal disease with the presence of multiple (usually large) hyperplastic/serrated colorectal polyps, usually with a pancolonic distribution. Histology reveals hyperplastic polyps, sessile serrated adenomas (most common), traditional serrated adenomas or mixed polyps. It is associated with an increased personal and familial (first-degree relatives) risk of colorectal cancer. There is evidence this disease is caused by heterozygous mutation in the RNF43 gene on chromosome 17q22. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hyperplastic polyposis syndrome | Is a | Familial multiple polyposis syndrome | true | Inferred relationship | Some | ||
Hyperplastic polyposis syndrome | Associated morphology | Multiple polyps | true | Inferred relationship | Some | 1 | |
Hyperplastic polyposis syndrome | Finding site | Structure of large intestine | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set