439702007: Hereditary protein S deficiency (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation fonctionnelle\Disorder of haemostatic system\...
• \thrombophilie\Hereditary thrombophilia (disorder)\Hereditary protein S deficiency (disorder)
• \thrombophilie\Protein S deficiency disease\Hereditary protein S deficiency (disorder)
• \Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Protein S deficiency disease\Hereditary protein S deficiency (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary thrombophilia (disorder)\Hereditary protein S deficiency (disorder)
• \Disease\Disorder of haemostatic system\thrombophilie\Hereditary thrombophilia (disorder)\Hereditary protein S deficiency (disorder)
• \Disease\Disorder of haemostatic system\thrombophilie\Protein S deficiency disease\Hereditary protein S deficiency (disorder)
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Deficiency of naturally occurring coagulation factor inhibitor\Protein S deficiency disease\Hereditary protein S deficiency (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2788437018	Hereditary protein S deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2791861013	Hereditary protein S deficiency	en	Synonym (core metadata concept)	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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