Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder) (8707426)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)
MAJOR CONCEPT File: 757, IEN: 7461921
DESIGNATION CODE
  • 3441990011
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE FULLY SPECIFIED NAME
SCOPE DIRECTLY LINKED
FORM FSN