441188004: Homozygous protein C deficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Functional finding\Disorder of haemostatic system\...
• \Thrombophilia\Hereditary thrombophilia\Hereditary protein C deficiency\Homozygous protein C deficiency
• \Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency\Homozygous protein C deficiency
• \Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Protein C deficiency disease\Hereditary protein C deficiency\Homozygous protein C deficiency
• \Disease\Genetic disease\Hereditary disease\Hereditary thrombophilia\Hereditary protein C deficiency\Homozygous protein C deficiency
• \Disease\Disorder of haemostatic system\Thrombophilia\Hereditary thrombophilia\Hereditary protein C deficiency\Homozygous protein C deficiency
• \Disease\Disorder of haemostatic system\Thrombophilia\Protein C deficiency disease\Hereditary protein C deficiency\Homozygous protein C deficiency
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Protein C deficiency disease\Hereditary protein C deficiency\Homozygous protein C deficiency

Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2788436010	Homozygous protein C deficiency (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
2794654010	Homozygous protein C deficiency	en	Synonym	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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