40855001: Hereditary factor VII deficiency disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\...
• \Prothrombin complex deficiency\Factor VII deficiency\Hereditary factor VII deficiency disease
• \Coagulation factor deficiency syndrome\Factor VII deficiency\Hereditary factor VII deficiency disease
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor VII deficiency disease
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor VII deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Prothrombin complex deficiency\Factor VII deficiency\Hereditary factor VII deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor VII deficiency\Hereditary factor VII deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor VII deficiency disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2789802015	Hereditary factor VII deficiency disease (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2794698010	Hereditary factor VII deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
492809012	Hereditary hypoproconvertinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
68137016	Hereditary factor VII deficiency syndrome	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
68138014	Hereditary hypoproconvertinemia	en	Synonym	Active	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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