Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency (8667532)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant hyperinsulinism due to sulfonylurea receptor 1 deficiency
MAJOR CONCEPT File: 757, IEN: 7452577
DESIGNATION CODE
  • 3308269015
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH