441189007: Homozygous protein S deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\...
• \Thrombophilia\Hereditary thrombophilia\Hereditary protein S deficiency\Homozygous protein S deficiency
• \Thrombophilia\Protein S deficiency disease\Hereditary protein S deficiency\Homozygous protein S deficiency
• \Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Protein S deficiency disease\Hereditary protein S deficiency\Homozygous protein S deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia\Hereditary protein S deficiency\Homozygous protein S deficiency
• \Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia\Hereditary protein S deficiency\Homozygous protein S deficiency
• \Disease\Disorder of hemostatic system\Thrombophilia\Protein S deficiency disease\Hereditary protein S deficiency\Homozygous protein S deficiency
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Protein S deficiency disease\Hereditary protein S deficiency\Homozygous protein S deficiency

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
2789761017	Homozygous protein S deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
2795208016	Homozygous protein S deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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