Homozygous prothrombin G20210A mutation (8629168)    EXPRESSIONS (757.01)

Name Value
DISPLAYABLE TEXT Homozygous prothrombin G20210A mutation
MAJOR CONCEPT File: 757, IEN: 7404493
DESIGNATION CODE
  • 2795461010
    CODING SYSTEM:   SCT
    HIERARCHY:   Disorder
TYPE SYNONYM
SCOPE DIRECTLY LINKED
FORM OTH