Familial benign copper deficiency (disorder) (8794138)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Familial benign copper deficiency (disorder)
MAJOR CONCEPT File: 757, IEN: 7482389
DESIGNATION CODE
  • 3642760016
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE FULLY SPECIFIED NAME
SCOPE DIRECTLY LINKED
FORM FSN