MODY 8 syndrome (Q102323): Difference between revisions

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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
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.