33297000: Hereditary factor II deficiency disease (disorder)

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

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
485473013	Hereditary hypoprothrombinaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
55565011	Hereditary factor II deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
55566012	Hereditary hypoprothrombinemia	en	Synonym	Active	Case insensitive	SNOMED CT core
764682017	Hereditary factor II 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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