Page values for "PTEN hamartoma tumor syndrome"
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"_pageData" values
1 row is stored for this page| Field | Field type | Value |
|---|---|---|
| _pageID | Integer | 863,692 |
| _pageName | Page | PTEN hamartoma tumor syndrome |
| _pageTitle | String | PTEN hamartoma tumor syndrome |
| _pageNamespace | Integer | 0 |
"definitions" values
1 row is stored for this page| Field | Field type | Value |
|---|---|---|
| Term | Page | PTEN hamartoma tumor syndrome |
| Short_definition | String | PTEN hamartoma tumor syndrome - group of inherited disorders caused by mutations (changes) in the PTEN gene. In people with PTEN hamartoma tumor syndrome, many benign (noncancerous) growths called hamartomas form in various parts of the body, particularly the skin, mouth, and gastrointestinal tract. |
| Type | Page | Cancer terms |
| Specialty | Page | Oncology |
| Language | Page | English |
| Source | Page | NCI |
| Comments | String |