439460003: Hereditary factor XIII A subunit and B subunit deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Factor XIII deficiency disease\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency
• \Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XIII deficiency disease\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII A subunit and B subunit deficiency

Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2789756019	Hereditary factor XIII A subunit and B subunit deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2790528015	Hereditary factor XIII type I deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2794133016	Hereditary factor XIII A subunit and B subunit deficiency	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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