Catalog

MODY 2 syndrome

No MMS code

Link to WHO Definition

MODY 2 syndrome – http://id.who.int/icd/entity/990655222

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.