Autosomal dominant myoglobinuria (disorder) (8708288)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant myoglobinuria (disorder)
MAJOR CONCEPT File: 757, IEN: 7462352
DESIGNATION CODE
  • 3446263014
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE FULLY SPECIFIED NAME
SCOPE DIRECTLY LINKED
FORM FSN