MODY 8 syndrome (Q102323): 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. CEL has been associated with a form of diabetes that has been characterised as "MODY8" by OMIM. It is very rare with five families reported to date. It is associated with exocrine pancreatic dysfunction.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_205210166 |
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| English | MODY 8 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. CEL has been associated with a form of diabetes that has been characterised as "MODY8" by OMIM. It is very rare with five families reported to date. It is associated with exocrine pancreatic dysfunction. |
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CID11:ID_205210166
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dki-india-ID_205210166
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Concluído
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15 August 2026
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