MODY 7 syndrome (Q102317): Difference between revisions
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15 August 2026
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Latest revision as of 19:15, 16 August 2026
This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. KLF11 has been associated with a form of diabetes that has been characterised as "MODY7" by OMIM.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1745614099 |
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| English | MODY 7 syndrome |
This refers to the hereditary form of diabetes caused by mutations in an autosomal dominant gene (sex independent, i.e. inherited from any of the parents) disrupting insulin production. KLF11 has been associated with a form of diabetes that has been characterised as "MODY7" by OMIM. |
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CID11:ID_1745614099
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dki-india-ID_1745614099
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Concluído
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15 August 2026
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