234444001: Congenital factor IX deficiency variant (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Factor IX deficiency\Hereditary factor IX deficiency disease\Congenital factor IX deficiency variant
• \Hemophilia\Hereditary factor IX deficiency disease\Congenital factor IX deficiency variant
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor IX deficiency disease\Congenital factor IX deficiency variant
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor IX deficiency\Hereditary factor IX deficiency disease\Congenital factor IX deficiency variant
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor IX deficiency disease\Congenital factor IX deficiency variant
• \Disease\Congenital disease\Hereditary factor IX deficiency disease\Congenital factor IX deficiency variant

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351266019	Congenital factor IX deficiency variant	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
622763015	Congenital factor IX deficiency variant (disorder)	en	Fully specified name	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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