438792009: hereditaire stollingsfactor IX-deficiëntie zonder 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 without inhibitor (disorder)

\Hemophilia\Hereditary factor IX deficiency disease\Hereditary factor IX deficiency disease without 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 without inhibitor (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Hereditary factor IX deficiency disease\Hereditary factor IX deficiency disease without 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 without 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 without 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 without inhibitor (disorder)	Is a	Hereditary factor IX deficiency disease	true	Inferred relationship	Some
Hereditary factor IX deficiency disease without inhibitor (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Hereditary factor IX deficiency disease without inhibitor (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Hereditary factor IX deficiency disease without inhibitor (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Moderate hereditary factor IX deficiency disease without inhibitor (disorder)	Is a	True	Hereditary factor IX deficiency disease without inhibitor (disorder)	Inferred relationship	Some
Severe hereditary factor IX deficiency disease without inhibitor (disorder)	Is a	True	Hereditary factor IX deficiency disease without inhibitor (disorder)	Inferred relationship	Some
Mild hereditary factor IX deficiency disease without inhibitor (disorder)	Is a	True	Hereditary factor IX deficiency disease without inhibitor (disorder)	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2788389010	Hereditary factor IX deficiency disease without inhibitor (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2791835014	Haemophilia B without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2791836010	Hemophilia B without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2795158019	Hereditary factor IX deficiency disease without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1468081000146118	hereditaire factor-IX-deficiëntie zonder inhibitor (aandoening)	nl	Fully specified name	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
1468091000146116	hereditaire factor-IX-deficiëntie zonder inhibitor	nl	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
3672921000146118	hemofilie B zonder remmer	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8586211000146118	hereditaire factor IX-deficiëntie zonder inhibitor (aandoening)	nl	Fully specified name	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8720471000146118	hereditaire factor IX-deficiëntie zonder inhibitor	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9891311000146118	hereditaire stollingsfactor IX-deficiëntie zonder inhibitor (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9892911000146112	hereditaire stollingsfactor IX-deficiëntie zonder inhibitor	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)