MODY 7 syndrome (Q102317)
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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 |
||
| 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. |
Statements
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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