234445000: Congenital factor IX deficiency with 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 with inhibitor
• \Haemophilia\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with 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 with inhibitor
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor
• \Disease\Congenital disease\Hereditary factor IX deficiency disease\Congenital factor IX deficiency with inhibitor

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
351267011	Congenital factor IX deficiency with inhibitor	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
622764014	Congenital factor IX deficiency with inhibitor (disorder)	en	Fully specified name	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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