| Display title | SPG15 (disease) |
| Default sort key | SPG15 (disease) |
| Page length (in bytes) | 12,205 |
| Namespace ID | 0 |
| Page ID | 71108211 |
| 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 | Q32142628 |
| Local description | Genetic disorder |
| Central description | A hereditary spastic paraplegia that has material basis in mutation in the ZFYVE26 gene on chromosome 14q24.1. |
| Page views in the past 30 days | |
| Edit | Allow all users (no expiry set) |
| Move | Allow all users (no expiry set) |
| Page creator | Curequester (talk | contribs) |
| Date of page creation | 14:08, 22 June 2022 |
| Latest editor | Citation bot (talk | contribs) |
| Date of latest edit | 21:02, 2 December 2023 |
| Total number of edits | 32 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (5) | This page is a member of 5 hidden categories (help):
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| Transcluded templates (48) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | |
