Display title | GM2-gangliosidosis, AB variant |
Default sort key | GM2-gangliosidosis, AB variant |
Page length (in bytes) | 8,621 |
Namespace ID | 0 |
Page ID | 2525674 |
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 | 6 |
Counted as a content page | Yes |
Wikidata item ID | Q5513688 |
Local description | Medical condition |
Central description | extremely rare, severe genetic disorder characterized by progressive neurological decline due to ganglioside activator deficiency |
Page image | ![Autorecessive.svg](//upload.wikimedia.org/wikipedia/commons/thumb/3/3e/Autorecessive.svg/220px-Autorecessive.svg.png) |
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Page creator | PDH (talk | contribs) |
Date of page creation | 05:04, 24 August 2005 |
Latest editor | Citation bot (talk | contribs) |
Date of latest edit | 01:53, 11 March 2023 |
Total number of edits | 135 |
Recent number of edits (within past 30 days) | 0 |
Recent number of distinct authors | 0 |
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Background color inline style rule exists without a corresponding text color | 1 |