Autosomal dominant hyperinsulinism due to sulphonylurea receptor 1 deficiency (8667533)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant hyperinsulinism due to sulphonylurea receptor 1 deficiency
MAJOR CONCEPT File: 757, IEN: 7452577
DESIGNATION CODE
  • 3308270019
    CODING SYSTEM:   SCT
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH
DEACTIVATION FLAG DEACTIVATED