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

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\...

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

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

\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder (disorder)\X-linked hereditary disease\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor
\Disease\Disorder of foetus and/or newborn\Congenital disease\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor
\Disease\Disorder of hemostatic system\Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system.\Coagulation factor deficiency syndrome\Haemophilia\Hereditary factor IX deficiency disease (disorder)\Hereditary factor IX deficiency disease with inhibitor

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor IX deficiency disease with inhibitor	Is a	Hereditary factor IX deficiency disease (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary factor IX deficiency disease with inhibitor	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hereditary factor IX deficiency disease with inhibitor	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary factor IX deficiency disease with inhibitor	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Severe hereditary factor IX deficiency disease with inhibitor (disorder)	Is a	True	Hereditary factor IX deficiency disease with inhibitor	Inferred relationship	Existential restriction modifier (core metadata concept)
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Is a	True	Hereditary factor IX deficiency disease with inhibitor	Inferred relationship	Existential restriction modifier (core metadata concept)
Moderate hereditary factor IX deficiency disease with inhibitor	Is a	True	Hereditary factor IX deficiency disease with inhibitor	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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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
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
6254761000241111	déficit héréditaire en facteur IX de la coagulation avec inhibiteur	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6254771000241115	maladie de Christmas avec inhibiteur	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6254781000241118	hémophilie B avec inhibiteur	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6254761000241111	déficit héréditaire en facteur IX de la coagulation avec inhibiteur	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6254771000241115	maladie de Christmas avec inhibiteur	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6254781000241118	hémophilie B avec inhibiteur	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module