Autosomal dominant hyperinsulinism due to Kir6.2 deficiency (8667531)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
MAJOR CONCEPT File: 757, IEN: 7452576
DESIGNATION CODE
  • 3308265014
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH