439459008: Hereditary factor XIII 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 B subunit deficiency
• \Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII B subunit deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor XIII deficiency disease\Hereditary factor XIII 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 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 B subunit deficiency

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2789395015	Hereditary factor XIII B subunit deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2790347018	Hereditary factor XIII B subunit deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2790348011	Hereditary factor XIII beta subunit deficiency	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
2790527013	Hereditary factor XIII type III 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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