45963004: Factor XI deficiency, type III (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\Blood coagulation disorder\...
• \Contact factor deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type III
• \Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type III
• \Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type III
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Hereditary factor XI deficiency disease\Factor XI deficiency, type III
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Contact factor deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type III
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor XI deficiency\Hereditary factor XI deficiency disease\Factor XI deficiency, type III
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor XI deficiency disease\Factor XI deficiency, type III
• \Disease\Congenital disease\Hereditary factor XI deficiency disease\Factor XI deficiency, type III

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
76639013	Factor XI deficiency, type III	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
783260019	Factor XI deficiency, type III (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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