| Display title | Medullary cystic kidney disease |
| Default sort key | Medullary Cystic Kidney Disease |
| Page length (in bytes) | 21,220 |
| Namespace ID | 0 |
| Page ID | 6484732 |
| 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 | 3 |
| Counted as a content page | Yes |
| Wikidata item ID | Q1916694 |
| Local description | Medical condition |
| Central description | inherited form of cystic kidney disease leading to fibrosis and impaired renal function that is caused by mutations in the UMOD gene, which encodes uromodulin/Tamm-Horsfall mucoprotein |
| 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 | Wouterstomp (talk | contribs) |
| Date of page creation | 19:55, 15 August 2006 |
| Latest editor | 108.31.101.142 (talk) |
| Date of latest edit | 23:55, 13 August 2024 |
| Total number of edits | 315 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (6) | This page is a member of 6 hidden categories (help):
|
| Transcluded templates (90) | Pages transcluded onto the current version of this page (help):
|
| Wikidata entities used in this page | |
| Duplicate IDs | 2 |
| Background color inline style rule exists without a corresponding text color | 1 |
