| Display title | Seckel syndrome |
| Default sort key | Seckel syndrome |
| Page length (in bytes) | 5,817 |
| Namespace ID | 0 |
| Page ID | 4624339 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of page watchers | 33 |
| Number of page watchers who visited in the last 30 days | There may or may not be a watching user visiting recent edits |
| Number of redirects to this page | 14 |
| Counted as a content page | Yes |
| Wikidata item ID | Q572169 |
| Local description | Medical condition |
| Central description | autosomal recessive disease characterized by intrauterine growth retardation and postnatal dwarfism with microcephaly and intellectual disability |
| 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 | Inferiority (talk | contribs) |
| Date of page creation | 11:03, 4 April 2006 |
| Latest editor | Ineffablebookkeeper (talk | contribs) |
| Date of latest edit | 16:55, 8 June 2024 |
| Total number of edits | 119 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (8) | This page is a member of 8 hidden categories (help):
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| Transcluded templates (79) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - Seckel syndrome
- Sitelink
- Statement: P1395
- Statement: P1461
- Title
- Statement: P486
- Statement: P5806
- Description: en
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| Background color inline style rule exists without a corresponding text color | 1 |
