440868005: lichte 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)\Mild hereditary factor IX deficiency disease with inhibitor (disorder)

\Hemophilia\Hereditary factor IX deficiency disease\Hereditary factor IX deficiency disease with inhibitor (disorder)\Mild 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)\Mild 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)\Mild 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)\Mild 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)\Mild 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
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Is a	Hereditary factor IX deficiency disease with inhibitor (disorder)	true	Inferred relationship	Some
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Mild hereditary factor IX deficiency disease with high response inhibitor	Is a	True	Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Inferred relationship	Some
Mild hereditary factor IX deficiency disease with low response inhibitor (disorder)	Is a	True	Mild 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
2790086014	Mild hereditary factor IX deficiency disease with inhibitor (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2791292015	Mild hemophilia B with inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2793938017	Mild hereditary factor IX deficiency disease with inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2794994014	Mild haemophilia B with inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6890071000146113	lichte 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)
8721401000146119	lichte 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)
8721411000146117	lichte erfelijke 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)
8721421000146110	lichte erfelijke factor IX-deficiëntieziekte met remmer	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9891401000146112	lichte 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)
9893061000146118	lichte 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)