234457009: hypofibrinogénémie (trouble)

• SNOMED CT Concept\constatation clinique\...
• \constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\...
• \Fibrinogen abnormality\Hypofibrinogenaemia
• \Coagulation factor deficiency syndrome\Factor I deficiency disease (disorder)\Hypofibrinogenaemia
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\...
• \Fibrinogen abnormality\Hypofibrinogenaemia
• \Coagulation factor deficiency syndrome\Factor I deficiency disease (disorder)\Hypofibrinogenaemia

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
351285016	Hypofibrinogenaemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
351286015	Hypofibrinogenemia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
622779019	Hypofibrinogenemia (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
819271000241114	hypofibrinogénémie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
819281000241111	hypofibrinogénémie (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

Back to Start