307115002: Homozygous Factor V Leiden mutation (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Homozygous Factor V Leiden mutation
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Homozygous Factor V Leiden mutation
• \Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Factor V Leiden mutation\Homozygous Factor V Leiden mutation

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
450295015	Homozygous Factor V Leiden mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
703597014	Homozygous Factor V Leiden mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1818721000195112	mutazione del fattore V Leiden omozigote	it	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5197881000241112	mutation homozygote du facteur V de Leiden	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
907881000195113	Homozygote Faktor-V-Leiden-Mutation	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

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