441189007: Homozygous protein S deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\...
• \Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary protein S deficiency (disorder)\Homozygous protein S deficiency
• \Thrombophilia\Protein S deficiency disease\Hereditary protein S deficiency (disorder)\Homozygous protein S deficiency
• \Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Deficiency of naturally occurring coagulation factor inhibitor\Protein S deficiency disease\Hereditary protein S deficiency (disorder)\Homozygous protein S deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Hereditary protein S deficiency (disorder)\Homozygous protein S deficiency
• \Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary protein S deficiency (disorder)\Homozygous protein S deficiency
• \Disease\Disorder of hemostatic system\Thrombophilia\Protein S deficiency disease\Hereditary protein S deficiency (disorder)\Homozygous protein S deficiency
• \Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Deficiency of naturally occurring coagulation factor inhibitor\Protein S deficiency disease\Hereditary protein S deficiency (disorder)\Homozygous protein S deficiency

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
2789761017	Homozygous protein S deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2795208016	Homozygous protein S deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2789761017	Homozygous protein S deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2795208016	Homozygous protein S deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5333461000241113	déficit en protéine S, homozygote	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5333461000241113	déficit en protéine S, homozygote	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

Back to Start