438372000: Hereditary factor IX deficiency disease with inhibitor (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)\Hereditary factor IX deficiency disease with inhibitor (disorder)

\Hemophilia\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor (disorder)

\Disease\Genetic disease\maladie héréditaire\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor (disorder)
\Disease\Disorder of haemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor (disorder)
\Disease\Congenital disease\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2009. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2787760013 Hereditary factor IX deficiency disease with inhibitor (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2791040019 Haemophilia B with inhibitor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2791041015 Hemophilia B with inhibitor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2791042010 Hereditary factor IX deficiency disease with inhibitor en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor IX deficiency disease with inhibitor (disorder)	interprète (attribut)	Hemostatic function (observable entity)	true	Inferred relationship	Some	1
Hereditary factor IX deficiency disease with inhibitor (disorder)	a pour interprétation (attribut)	anormal	true	Inferred relationship	Some	1
Hereditary factor IX deficiency disease with inhibitor (disorder)	est un(e) (attribut)	Hereditary factor IX deficiency disease (disorder)	true	Inferred relationship	Some
Hereditary factor IX deficiency disease with inhibitor (disorder)	survenue (attribut)	congénital	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Severe hereditary factor IX deficiency disease with inhibitor (disorder)	est un(e) (attribut)	True	Hereditary factor IX deficiency disease with inhibitor (disorder)	Inferred relationship	Some
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	est un(e) (attribut)	True	Hereditary factor IX deficiency disease with inhibitor (disorder)	Inferred relationship	Some
Moderate hereditary factor IX deficiency disease with inhibitor (disorder)	est un(e) (attribut)	True	Hereditary factor IX deficiency disease with inhibitor (disorder)	Inferred relationship	Some

This concept is not in any reference sets