| Display title | Simpson–Golabi–Behmel syndrome |
| Default sort key | Simpson-Golabi-Behmel syndrome |
| Page length (in bytes) | 14,072 |
| Namespace ID | 0 |
| Page ID | 4166656 |
| 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 | 8 |
| Counted as a content page | Yes |
| Wikidata item ID | Q478891 |
| Local description | Congenital disorder |
| Central description | X-linked disease characterized by pre- and postnatal overgrowth and craniofacial, skeletal, cardiac and renal abnormalities |
| Page image |  |
| Page views in the past 30 days | |
| Edit | Allow all users (no expiry set) |
| Move | Allow all users (no expiry set) |
| Page creator | Sok122 (talk | contribs) |
| Date of page creation | 01:00, 23 February 2006 |
| Latest editor | 167.201.243.136 (talk) |
| Date of latest edit | 22:00, 15 March 2024 |
| Total number of edits | 173 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (5) | This page is a member of 5 hidden categories (help):
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| Transcluded templates (75) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | |
| Background color inline style rule exists without a corresponding text color | 1 |
