MODY 2 syndrome (Q102304): Difference between revisions
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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. This form is due to any of several mutations in the GCK gene. 30%–70% cases. Mild fasting hyperglycaemia throughout life. Small rise on glucose loading.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_990655222 |
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| English | MODY 2 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. This form is due to any of several mutations in the GCK gene. 30%–70% cases. Mild fasting hyperglycaemia throughout life. Small rise on glucose loading. |
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CID11:ID_990655222
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