Prothrombin G20210A mutation

Prothrombin G20210A mutation (disorder)

active

Code	`440989002`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20090131

Parents (2)

11164009Autosomal dominant hereditary disorder disorder
439698008Hereditary thrombophilia disorder

Children (2)

441421001Heterozygous prothrombin G20210A mutation disorder
441420000Homozygous prothrombin G20210A mutation disorder