37350004: Hereditary factor X deficiency disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of hemostatic system\Blood coagulation disorder\...
• \Prothrombin complex deficiency\Factor X deficiency\Hereditary factor X deficiency disease
• \Coagulation factor deficiency syndrome\Factor X deficiency\Hereditary factor X deficiency disease
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor X deficiency disease
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor X deficiency disease
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor X deficiency disease
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Prothrombin complex deficiency\Factor X deficiency\Hereditary factor X deficiency disease
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor X deficiency\Hereditary factor X deficiency disease
• \Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor X 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
62309012	Hereditary factor X deficiency disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
62310019	Hereditary Stuart factor deficiency disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
62311015	Hereditary Stuart-Prower deficiency disease	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
769207019	Hereditary factor X 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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