43217004: Hereditary factor XII deficiency disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\...
• \Contact factor deficiency\Factor XII deficiency disease\Hereditary factor XII deficiency disease
• \Coagulation factor deficiency syndrome\Factor XII deficiency disease\Hereditary factor XII deficiency disease
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XII deficiency disease
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor XII deficiency disease
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XII deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Contact factor deficiency\Factor XII deficiency disease\Hereditary factor XII deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XII deficiency disease\Hereditary factor XII deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor XII deficiency disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
72102014	Hereditary factor XII deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
72103016	Hereditary Hageman factor deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
780203015	Hereditary factor XII deficiency disease (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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