441192006: lichte hereditaire stollingsfactor IX-deficiëntieziekte 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)\Mild hereditary factor IX deficiency disease without inhibitor (disorder)

\Hemophilia\Hereditary factor IX deficiency disease\Hereditary factor IX deficiency disease without inhibitor (disorder)\Mild 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)\Mild 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)\Mild 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)\Mild 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)\Mild 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
Mild hereditary factor IX deficiency disease without inhibitor (disorder)	Is a	Hereditary factor IX deficiency disease without inhibitor (disorder)	true	Inferred relationship	Some
Mild hereditary factor IX deficiency disease without inhibitor (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	2
Mild hereditary factor IX deficiency disease without inhibitor (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Mild hereditary factor IX deficiency disease without inhibitor (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
2789838010	Mild hereditary factor IX deficiency disease without inhibitor (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2790744010	Mild hereditary factor IX deficiency disease without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2793597019	Mild haemophilia B without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2794748017	Mild hemophilia B without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6890281000146116	lichte hemofilie B 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)
8721451000146118	lichte hereditaire factor IX-deficiëntieziekte 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)
8721461000146115	lichte erfelijke factor IX-deficiëntieziekte 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)
8721471000146114	lichte genetische factor IX-deficiëntieziekte 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)
9891471000146117	lichte hereditaire stollingsfactor IX-deficiëntieziekte 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)
9893071000146112	lichte hereditaire stollingsfactor IX-deficiëntieziekte 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)