| Display title | Galloway–Mowat syndrome |
| Default sort key | Galloway–Mowat syndrome |
| Page length (in bytes) | 6,666 |
| Namespace ID | 0 |
| Page ID | 4293651 |
| 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 | 5 |
| Counted as a content page | Yes |
| Wikidata item ID | Q4357083 |
| Local description | Medical condition |
| Central description | autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome |
| 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 | Dwaipayanc (talk | contribs) |
| Date of page creation | 07:53, 6 March 2006 |
| Latest editor | WikiCleanerBot (talk | contribs) |
| Date of latest edit | 18:15, 25 March 2024 |
| Total number of edits | 78 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (9) | This page is a member of 9 hidden categories (help):
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| Transcluded templates (74) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - Galloway-Mowat syndrome
- Title
- Description: en
- Statement: P1995
- Statement: P5806
- Statement: P1461
- Statement: P1395
- Sitelink
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| Background color inline style rule exists without a corresponding text color | 1 |
