234444001: Congenital factor IX deficiency variant (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\...
• \Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease (disorder)\Congenital factor IX deficiency variant
• \Haemophilia\Hereditary factor IX deficiency disease (disorder)\Congenital factor IX deficiency variant
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder (disorder)\X-linked hereditary disease\Hereditary factor IX deficiency disease (disorder)\Congenital factor IX deficiency variant
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary factor IX deficiency disease (disorder)\Congenital factor IX deficiency variant
• \Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease (disorder)\Congenital factor IX deficiency variant
• \Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor IX deficiency disease (disorder)\Congenital factor IX deficiency variant

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
351266019	Congenital factor IX deficiency variant	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
622763015	Congenital factor IX deficiency variant (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
351266019	Congenital factor IX deficiency variant	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
622763015	Congenital factor IX deficiency variant (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
127141000077117	variante de déficience congénitale en facteur IX	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
127141000077117	variante de déficience congénitale en facteur IX	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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