33297000: Hereditary factor II deficiency disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic 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 hemostatic system\Blood coagulation disorder\Prothrombin complex deficiency\Factor II deficiency\Hereditary factor II deficiency disease
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor II deficiency\Hereditary factor II deficiency disease
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor II 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
55565011	Hereditary factor II deficiency disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
55566012	Hereditary hypoprothrombinemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
485473013	Hereditary hypoprothrombinaemia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
764682017	Hereditary factor II 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

Back to Start