441420000: Homozygous prothrombin G20210A mutation (disorder)

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

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

Descriptions:

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

Expanded Value Set

Reference Sets

Description inactivation indicator reference set

GB English

US English

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