Autosomal dominant vitreoretinochoroidopathy (8661592)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Autosomal dominant vitreoretinochoroidopathy
MAJOR CONCEPT File: 757, IEN: 7442877
DESIGNATION CODE
  • 3047555016
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH