Catalog

MODY 3 syndrome

No MMS code

Link to WHO Definition

MODY 3 syndrome – http://id.who.int/icd/entity/964882179

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.