Familial benign copper deficiency (8794137)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Familial benign copper deficiency
MAJOR CONCEPT File: 757, IEN: 7482389
DESIGNATION CODE
  • 3642758018
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE MAJOR CONCEPT
SCOPE DIRECTLY LINKED
FORM MAJ