426199009: Congenital factor IX deficiency without inhibitor (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Factor IX deficiency\Hereditary factor IX deficiency disease\Congenital factor IX deficiency without inhibitor
• \Haemophilia\Hereditary factor IX deficiency disease\Congenital factor IX deficiency without inhibitor
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor IX deficiency disease\Congenital factor IX deficiency without inhibitor
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor IX deficiency\Hereditary factor IX deficiency disease\Congenital factor IX deficiency without inhibitor
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor IX deficiency disease\Congenital factor IX deficiency without inhibitor
• \Disease\Congenital disease\Hereditary factor IX deficiency disease\Congenital factor IX deficiency without inhibitor

Status: current, Primitive. Date: 31-Jul 2007. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2662913011	Congenital factor IX deficiency without inhibitor (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2674750019	Congenital factor IX deficiency without inhibitor	en	Synonym	Active	Initial character case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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