MODY 3 syndrome (Q102295): Difference between revisions
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15 August 2026
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Latest revision as of 19:14, 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. Mutations of the HNF1? gene (a homeobox gene). 30%–70% cases. Tend to be responsive to sulfonylureas. Low renal threshold for glucose.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_964882179 |
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| English | MODY 3 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. Mutations of the HNF1? gene (a homeobox gene). 30%–70% cases. Tend to be responsive to sulfonylureas. Low renal threshold for glucose. |
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CID11:ID_964882179
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dki-india-ID_964882179
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Concluído
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15 August 2026
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