438372000: hereditaire stollingsfactor IX-deficiëntieziekte met inhibitor (aandoening)

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

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...

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

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

\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor IX deficiency disease\Hereditary factor IX deficiency disease with inhibitor (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary factor IX deficiency disease\Hereditary factor IX deficiency disease with inhibitor (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor IX deficiency (disorder)\Hereditary factor IX deficiency disease\Hereditary factor IX deficiency disease with inhibitor (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor IX deficiency disease\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:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary factor IX deficiency disease with inhibitor (disorder)	Is a	Hereditary factor IX deficiency disease	true	Inferred relationship	Some
Hereditary factor IX deficiency disease with inhibitor (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Hereditary factor IX deficiency disease with inhibitor (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary factor IX deficiency disease with inhibitor (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	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 (disorder)	Inferred relationship	Some
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Is a	True	Hereditary factor IX deficiency disease with inhibitor (disorder)	Inferred relationship	Some
Moderate hereditary factor IX deficiency disease with inhibitor (disorder)	Is a	True	Hereditary factor IX deficiency disease with inhibitor (disorder)	Inferred relationship	Some

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
6126121000146111	hemofilie B met inhibitor	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8720491000146119	genetische factor IX-deficiëntieziekte met inhibitor	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8720501000146112	erfelijke factor IX-deficiëntieziekte met antilichaam	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8720511000146114	hereditaire factor IX-deficiëntieziekte met inhibitor	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9891281000146116	hereditaire stollingsfactor IX-deficiëntieziekte met inhibitor (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9892921000146119	hereditaire stollingsfactor IX-deficiëntieziekte met inhibitor	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)