Page values for "Cowden Syndrome"
Jump to navigation
Jump to search
"_pageData" values
1 row is stored for this page| Field | Field type | Value |
|---|---|---|
| _pageID | Integer | 858,156 |
| _pageName | Page | Cowden Syndrome |
| _pageTitle | String | Cowden Syndrome |
| _pageNamespace | Integer | 0 |
"definitions" values
1 row is stored for this page| Field | Field type | Value |
|---|---|---|
| Term | Page | Cowden Syndrome |
| Short_definition | String | Cowden Syndrome - (pronounced) (KOW-den SIN-drome) A rare inherited disorder characterized by the presence of many benign (noncancerous) growths called hamartomas and an increased risk of cancer. Hamartomas form in various parts of the body, particularly in the skin, mouth, and gastrointestinal trac |
| Type | Page | Cancer terms |
| Specialty | Page | Oncology |
| Language | Page | English |
| Source | Page | NCI |
| Comments | String |