Display title | Galloway–Mowat syndrome |
Default sort key | Galloway–Mowat syndrome |
Page length (in bytes) | 6,666 |
Namespace ID | 0 |
Page ID | 4293651 |
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 | 5 |
Counted as a content page | Yes |
Wikidata item ID | Q4357083 |
Local description | Medical condition |
Central description | autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome |
Page image | ![Autosomal recessive - en.svg](//upload.wikimedia.org/wikipedia/commons/thumb/f/f1/Autosomal_recessive_-_en.svg/220px-Autosomal_recessive_-_en.svg.png) |
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Page creator | Dwaipayanc (talk | contribs) |
Date of page creation | 07:53, 6 March 2006 |
Latest editor | WikiCleanerBot (talk | contribs) |
Date of latest edit | 18:15, 25 March 2024 |
Total number of edits | 78 |
Recent number of edits (within past 30 days) | 0 |
Recent number of distinct authors | 0 |
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Wikidata entities used in this page | - Galloway-Mowat syndrome
- Title
- Description: en
- Statement: P1995
- Statement: P5806
- Statement: P1461
- Statement: P1395
- Sitelink
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Background color inline style rule exists without a corresponding text color | 1 |