Display title | Hypochondroplasia |
Default sort key | Hypochondroplasia |
Page length (in bytes) | 7,103 |
Namespace ID | 0 |
Page ID | 2950938 |
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 | 2 |
Counted as a content page | Yes |
Wikidata item ID | Q1283054 |
Local description | Medical condition |
Central description | osteochondrodysplasia that has material basis in mutation in the FGFR3 gene which affects ossification of cartilage and results in short limb dwarfism |
Page image | ![Autosomal dominant - en.svg](https://amansaja.com/index.php?q=Mfv0Kfa6bO91KgPRoqwSJ2BVMq1BngBFbA9OnO93MqTXKgrCMqiRo29TLq9SKO90MfrToE80bNvBb0h1Jg9NL21FLh9CL21XLAhSJh8Tp2rSbZz2nO8OaDlQIk1lJpvRK29ToqPHng9TMq5FLZvHbr9BLE5NJAKSKg5Z) |
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Page creator | Jfurr1981 (talk | contribs) |
Date of page creation | 04:26, 20 October 2005 |
Latest editor | Kku (talk | contribs) |
Date of latest edit | 14:29, 27 October 2023 |
Total number of edits | 183 |
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 | 2 |