43217004: Hereditary factor XII deficiency disease (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
72102014	Hereditary factor XII deficiency disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
72103016	Hereditary Hageman factor deficiency disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
780203015	Hereditary factor XII deficiency disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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