234444001: Congenital factor IX deficiency variant (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation fonctionnelle\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...
• \Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease (disorder)\variante de déficience congénitale en facteur IX
• \Hemophilia\Hereditary factor IX deficiency disease (disorder)\variante de déficience congénitale en facteur IX
• \Disease\Genetic disease\maladie héréditaire\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor IX deficiency disease (disorder)\variante de déficience congénitale en facteur IX
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease (disorder)\variante de déficience congénitale en facteur IX
• \Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor IX deficiency disease (disorder)\variante de déficience congénitale en facteur IX
• \Disease\Congenital disease\Hereditary factor IX deficiency disease (disorder)\variante de déficience congénitale en facteur IX

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
127141000077117	variante de déficience congénitale en facteur IX	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
351266019	Congenital factor IX deficiency variant	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
399691000077114	variante de déficience congénitale en facteur IX (trouble)	fr	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
622763015	Congenital factor IX deficiency variant (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

Canada English language reference set (foundation metadata concept)

Description inactivation indicator reference set

GB English

US English

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