441190003: ernstige 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)\Severe hereditary factor IX deficiency disease without inhibitor (disorder)

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Description inactivation indicator reference set

GB English

US English

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Id	Description	Lang	Type	Status	Case?	Module
2789418016	Severe hereditary factor IX deficiency disease without inhibitor (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2792427019	Severe haemophilia B without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2794172017	Severe hereditary factor IX deficiency disease without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2794173010	Severe hemophilia B without inhibitor	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6147151000146119	ernstige 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)
8713981000146111	ernstige 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)
8713991000146113	ernstige erfelijke factor IX-deficiëntieziekte zonder antilichaam	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8714001000146116	ernstige 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)
9891451000146113	ernstige 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)
9892521000146114	ernstige 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)