31925001: Hereditary factor I deficiency disease (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\...
• \Fibrinogen abnormality\anomalie congénitale du fibrinogène\Hereditary factor I deficiency disease
• \Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease
• \Disease\Genetic disease\maladie héréditaire\Hereditary coagulation factor deficiency\Hereditary factor I deficiency disease
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Fibrinogen abnormality\anomalie congénitale du fibrinogène\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\anomalie congénitale du fibrinogène\Hereditary factor I deficiency disease

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
485080016	Hereditary hypofibrinogenaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
53348015	Hereditary factor I deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
53350011	Hereditary hypofibrinogenemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
763149014	Hereditary factor I deficiency disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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