Information for "Calpainopathy"
Basic information
| Display title | Calpainopathy |
| Default sort key | Calpainopathy |
| Page length (in bytes) | 11,449 |
| Namespace ID | 0 |
| Page ID | 63872064 |
| 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 | Q17177467 |
| Local description | Medical condition |
| Central description | autosomal recessive limb-girdle muscular dystrophy that has material basis in homozygous or compound heterozygous mutation in the gene encoding the proteolytic enzyme calpain-3 (CAPN3) on chromosome 15q15 |
| Page image |  |
| Page views in the past 30 days |
Page protection
| Edit | Allow all users (no expiry set) |
| Move | Allow all users (no expiry set) |
Edit history
| Page creator | Lukelahood (talk | contribs) |
| Date of page creation | 00:16, 6 May 2020 |
| Latest editor | Beland (talk | contribs) |
| Date of latest edit | 20:28, 25 April 2024 |
| Total number of edits | 44 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
Page properties
Lint errors
| Background color inline style rule exists without a corresponding text color | 1 |