441420000: Homozygous prothrombin G20210A mutation (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia\Prothrombin G20210A mutation\Homozygous prothrombin G20210A mutation
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia\Prothrombin G20210A mutation\Homozygous prothrombin G20210A mutation
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Prothrombin G20210A mutation\Homozygous prothrombin G20210A mutation
• \Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia\Prothrombin G20210A mutation\Homozygous prothrombin G20210A mutation

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2009. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2787282019	Homozygous prothrombin G20210A mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
2795461010	Homozygous prothrombin G20210A mutation	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

Back to Start