| Display title | GRIN2B-related neurodevelopmental disorder |
| Default sort key | GRIN2B-related neurodevelopmental disorder |
| Page length (in bytes) | 5,953 |
| Namespace ID | 0 |
| Page ID | 71202716 |
| 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 | 0 |
| Counted as a content page | Yes |
| Wikidata item ID | Q50349610 |
| Local description | Medical condition |
| Central description | An autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of GRIN2B on chromosome 12p13.1. |
| Page views in the past 30 days | |
| Edit | Allow all users (no expiry set) |
| Move | Allow all users (no expiry set) |
| Page creator | Rollcloud (talk | contribs) |
| Date of page creation | 18:08, 1 July 2022 |
| Latest editor | Ozzie10aaaa (talk | contribs) |
| Date of latest edit | 22:30, 26 July 2022 |
| Total number of edits | 20 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
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| Transcluded templates (42) | Pages transcluded onto the current version of this page (help):
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