31925001: Hereditary factor I deficiency disease (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\...
• \Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease
• \Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Fibrinogen abnormality\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease
• \Disease\Congenital disease\Congenital fibrinogen abnormality\Hereditary factor I deficiency disease

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
485080016	Hereditary hypofibrinogenaemia	en	Synonym	Active	Case insensitive	SNOMED CT core
53348015	Hereditary factor I deficiency disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
53350011	Hereditary hypofibrinogenemia	en	Synonym	Active	Case insensitive	SNOMED CT core
763149014	Hereditary factor I 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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