37350004: Hereditary factor X deficiency disease (disorder)

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

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
62309012	Hereditary factor X deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
62310019	Hereditary Stuart factor deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
62311015	Hereditary Stuart-Prower deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
769207019	Hereditary factor X 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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