Display title | Pachyonychia congenita |
Default sort key | Pachyonychia congenita |
Page length (in bytes) | 13,166 |
Namespace ID | 0 |
Page ID | 9345204 |
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 | 23 |
Counted as a content page | Yes |
Wikidata item ID | Q3360152 |
Local description | Medical condition |
Central description | rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes |
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Edit history
Page creator | Irwin McLean (talk | contribs) |
Date of page creation | 11:58, 6 February 2007 |
Latest editor | A.sav (talk | contribs) |
Date of latest edit | 06:06, 11 April 2024 |
Total number of edits | 183 |
Recent number of edits (within past 30 days) | 1 |
Recent number of distinct authors | 1 |
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Wikidata entities used in this page | - medical genetics
- pachyonychia congenita
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- Sitelink
- Some statements
- Description: en
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