441101007: Heterozygous protein C deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\...
• \Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)
• \Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)
• \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 C deficiency disease\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)
• \Disease\Disorder of hemostatic system\Thrombophilia\Hereditary thrombophilia (disorder)\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)
• \Disease\Disorder of hemostatic system\Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (disorder)
• \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 C deficiency disease\Hereditary protein C deficiency (disorder)\Heterozygous protein C deficiency (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
2790011014	Heterozygous protein C deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2791270019	Heterozygous protein C deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790011014	Heterozygous protein C deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2791270019	Heterozygous protein C deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5333401000241114	déficit en protéine C, hétérozygote	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5333401000241114	déficit en protéine C, hétérozygote	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

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