Information for "Meckel–Gruber syndrome"
Basic information
| Display title | Meckel–Gruber syndrome |
| Default sort key | Meckel-Gruber syndrome |
| Page length (in bytes) | 11,118 |
| Namespace ID | 0 |
| Page ID | 9446925 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of page watchers | Fewer than 30 watchers |
| Number of redirects to this page | 10 |
| Counted as a content page | Yes |
| Wikidata item ID | Q1915681 |
| Local description | Medical condition |
| Central description | a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia. |
| Page image |  |
| Page views in the past 30 days |
Page protection
| Edit | Allow all users (no expiry set) |
| Move | Allow all users (no expiry set) |
Edit history
| Page creator | WiiAlbanyGirl (talk | contribs) |
| Date of page creation | 18:51, 11 February 2007 |
| Latest editor | Parcynthia (talk | contribs) |
| Date of latest edit | 00:12, 3 December 2024 |
| Total number of edits | 182 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
Page properties
Lint errors
| Background color inline style rule exists without a corresponding text color | 1 |