1285665003: lichte hereditaire stollingsfactor IX-deficiëntieziekte met inhibitor met hoge respons (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)\Mild hereditary factor IX deficiency disease with high response inhibitor

\Hemophilia\Hereditary factor IX deficiency disease\Hereditary factor IX deficiency disease with inhibitor (disorder)\Mild hereditary factor IX deficiency disease with inhibitor (disorder)\Mild hereditary factor IX deficiency disease with high response inhibitor

\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)\Mild hereditary factor IX deficiency disease with high response inhibitor
\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)\Mild hereditary factor IX deficiency disease with high response inhibitor
\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)\Mild hereditary factor IX deficiency disease with high response inhibitor
\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)\Mild hereditary factor IX deficiency disease with high response inhibitor

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2023. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Mild hereditary factor IX deficiency disease with high response inhibitor	Is a	Mild hereditary factor IX deficiency disease with inhibitor (disorder)	true	Inferred relationship	Some
Mild hereditary factor IX deficiency disease with high response inhibitor	Occurrence	Congenital	true	Inferred relationship	Some	2
Mild hereditary factor IX deficiency disease with high response inhibitor	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Mild hereditary factor IX deficiency disease with high response inhibitor	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
5249812016	Mild hereditary factor IX deficiency disease with high response inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5249813014	Mild hereditary factor IX deficiency disease with high response inhibitor (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
14420401000146116	lichte hemofilie B met remmende antistof met hoge respons	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14420411000146119	lichte hereditaire stollingsfactor IX-deficiëntieziekte met inhibitor met hoge respons	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14420421000146112	lichte hereditaire stollingsfactor IX-deficiëntieziekte met inhibitor met hoge respons (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14420431000146114	milde erfelijke factor IX-deficiëntieziekte met remmer met hoge respons	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)