26029002: lichte hereditaire stollingsfactor VIII-deficiëntieziekte (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Functional finding\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\...

\Factor VIII deficiency\Hereditary factor VIII deficiency disease\Mild hereditary factor VIII deficiency disease (disorder)

\Hemophilia\Hereditary factor VIII deficiency disease\Mild hereditary factor VIII deficiency disease (disorder)

\Hereditary coagulation factor deficiency\Hereditary factor VIII deficiency disease\Mild hereditary factor VIII deficiency disease (disorder)

\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Hereditary factor VIII deficiency disease\Mild hereditary factor VIII deficiency disease (disorder)
\Disease\Genetic disease\Hereditary disease\Hereditary coagulation factor deficiency\Hereditary factor VIII deficiency disease\Mild hereditary factor VIII deficiency disease (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Factor VIII deficiency\Hereditary factor VIII deficiency disease\Mild hereditary factor VIII deficiency disease (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hemophilia\Hereditary factor VIII deficiency disease\Mild hereditary factor VIII deficiency disease (disorder)
\Disease\Disorder of hemostatic system\Blood coagulation disorder\Coagulation factor deficiency syndrome\Hereditary coagulation factor deficiency\Hereditary factor VIII deficiency disease\Mild hereditary factor VIII deficiency disease (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Mild hereditary factor VIII deficiency disease (disorder)	Is a	Hereditary factor VIII deficiency disease	true	Inferred relationship	Some
Mild hereditary factor VIII deficiency disease (disorder)	Finding site	Entire hematological system (body structure)	false	Inferred relationship	Some
Mild hereditary factor VIII deficiency disease (disorder)	Severity	Mild	false	Inferred relationship	Some
Mild hereditary factor VIII deficiency disease (disorder)	Finding site	Body system structure	false	Inferred relationship	Some
Mild hereditary factor VIII deficiency disease (disorder)	Has definitional manifestation	Hemostatic system finding	false	Inferred relationship	Some
Mild hereditary factor VIII deficiency disease (disorder)	Interprets	Hemostatic function	true	Inferred relationship	Some	1
Mild hereditary factor VIII deficiency disease (disorder)	Has interpretation	Abnormal	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Mild hereditary factor VIII deficiency disease with inhibitor (disorder)	Is a	True	Mild hereditary factor VIII deficiency disease (disorder)	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
43600019	Mild hemophilia A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
483093012	Mild haemophilia A	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2787929017	Mild hereditary factor VIII deficiency disease (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
2792392016	Mild hereditary factor VIII deficiency disease	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6890381000146112	lichte hemofilie A	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8721481000146111	lichte hereditaire factor VIII-deficiëntieziekte	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8721491000146113	lichte genetische factor VIII-deficiëntieziekte	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8721501000146115	lichte erfelijke factor VIII-deficiëntieziekte	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9890781000146117	lichte hereditaire stollingsfactor VIII-deficiëntieziekte (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9893081000146114	lichte hereditaire stollingsfactor VIII-deficiëntieziekte	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
2884517012	Mild disease manifests factor VIII activity of greater than 5% of normal	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core